Fresh Recalls

Latest recalls — page 3

Browse the most recent U.S. safety recalls in our connected official government data.

3,525 recalls in our current data. Showing 201–300, newest first.

FDA Class II · Medical device · October 7, 2026

Computed Tomography X-ray System recall — Shanghai United Imaging Healthcare Co., Ltd.

Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …

Company / brand: Shanghai United Imaging Healthcare Co recalls

Official ID Z-3280-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Computed Tomography X-ray System recall — Shanghai United Imaging Healthcare Co., Ltd.

Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …

Company / brand: Shanghai United Imaging Healthcare Co recalls

Official ID Z-3279-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Computed Tomography X-ray System recall — Shanghai United Imaging Healthcare Co., Ltd.

Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …

Company / brand: Shanghai United Imaging Healthcare Co recalls

Official ID Z-3278-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Computed Tomography X-ray System recall — Shanghai United Imaging Healthcare Co., Ltd.

Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …

Company / brand: Shanghai United Imaging Healthcare Co recalls

Official ID Z-3277-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Philips IntraSight Plus REF recall — Volcano Corp

Software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment.

Company / brand: Volcano recalls

Official ID Z-3276-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number recall — Bard Peripheral Vascular Inc

Breast biopsy and tissue removal system may experience the following errors: 1) Probe calibration and /or handheld driver failure (code HH01-00020009) , 2) Pressure sensor (code E0…

Company / brand: Bard Peripheral Vascular recalls

Official ID Z-3275-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Fisher Scientific Sure-Vue Urine hCG recall — Alere San Diego, Inc.

hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.

Company / brand: Alere San Diego recalls

Official ID Z-3274-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Fisher Scientific Sure-Vue Urine hCG Strip recall — Alere San Diego, Inc.

hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.

Company / brand: Alere San Diego recalls

Official ID Z-3273-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Fisher Scientific Sure-Vue Serum/Urine hCG recall — Alere San Diego, Inc.

hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.

Company / brand: Alere San Diego recalls

Official ID Z-3272-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

McKesson CONSULT hCG Urine Cassette recall — Alere San Diego, Inc.

hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.

Company / brand: Alere San Diego recalls

Official ID Z-3271-2026 · Official record ↗

FDA Class III · Medical device · October 7, 2026

HeartSine samaritan PAD (Public Access Defibrillator) recall — HeartSine Technologies Ltd

Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check.

Company / brand: HeartSine Technologies recalls

Official ID Z-3270-2026 · Official record ↗

FDA Class I · Medical device · October 7, 2026

VentStar Resus Neo recall — Draeger, Inc.

Potential cracks in the hose, which could lead to leakage or the hose falling off.

Company / brand: Draeger recalls

Official ID Z-3252-2026 · Official record ↗

FDA Class I · Medical device · October 7, 2026

Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED recall — Medline Industries, LP

Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, spar…

Company / brand: Medline Industries recalls

Official ID Z-3228-2026 · Official record ↗

FDA Class I · Medical device · October 7, 2026

Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories recall — Medline Industries, LP

Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, spar…

Company / brand: Medline Industries recalls

Official ID Z-3227-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Philips Medical Systems Technologies Ltd recall — Philips North America Llc

The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached. This may result in t…

Company / brand: Philips North America recalls

Official ID Z-3155-2026 · Official record ↗

FDA Class II · Medical device · October 7, 2026

NovaSeq 6000Dx including DRAGEN Server recall — Illumina, Inc.

Retrospectively reported correction for an instrument intended for targeted sequencing of DNA libraries from human genomic DNA used with in vitro diagnostic assays has a server wit…

Company / brand: Illumina recalls

Official ID Z-0068-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — Custom Interventional Pain Management, LLC

Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits.

Company / brand: Custom Interventional Pain Management recalls

Official ID Z-0067-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0066-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0065-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0064-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0063-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0062-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0061-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0060-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0059-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0058-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0057-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0056-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0055-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0054-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0053-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0052-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0051-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0050-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0049-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0048-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0047-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0046-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0045-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0044-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0043-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0042-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0041-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0040-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0039-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0038-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0037-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0036-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0035-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0034-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0033-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0032-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0031-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0030-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0029-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0028-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0027-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0026-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0025-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0024-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0023-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0022-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0021-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0020-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0019-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0018-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0017-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0016-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0015-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0014-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0013-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0012-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0011-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0010-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0009-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0008-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0007-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0006-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0005-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0004-2027 · Official record ↗

FDA Class II · Medical device · October 7, 2026

Brand Name recall — ASP Global, LLC.

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5…

Company / brand: ASP Global recalls

Official ID Z-0003-2027 · Official record ↗

FDA Class I · Food · October 7, 2026

Todd's Seeds Variety Pack of Sprouting Seeds - Broccoli recall — TODD'S SEEDS LLC

Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)

Company / brand: TODD'S SEEDS recalls

Official ID H-1409-2026 · Official record ↗

FDA Class I · Food · October 7, 2026

Todd's Seeds Alfalfa & Mung Bundle (1lb each) recall — TODD'S SEEDS LLC

Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)

Company / brand: TODD'S SEEDS recalls

Official ID H-1408-2026 · Official record ↗

FDA Class I · Food · October 7, 2026

Todd's Seeds Salad Sprouting Mixture - Broccoli recall — TODD'S SEEDS LLC

Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)

Company / brand: TODD'S SEEDS recalls

Official ID H-1407-2026 · Official record ↗

FDA Class I · Food · October 7, 2026

Todd's Seeds Sprouting Seed Mix - Broccoli recall — TODD'S SEEDS LLC

Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)

Company / brand: TODD'S SEEDS recalls

Official ID H-1406-2026 · Official record ↗

FDA Class I · Food · October 7, 2026

Todd's Seeds Broccoli & Friends Sprouting Seed Mix - Broccoli recall — TODD'S SEEDS LLC

Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)

Company / brand: TODD'S SEEDS recalls

Official ID H-1405-2026 · Official record ↗

FDA Class I · Food · October 7, 2026

Todd's Seeds Alfalfa Sprouting Seeds recall — TODD'S SEEDS LLC

Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)

Company / brand: TODD'S SEEDS recalls

Official ID H-1404-2026 · Official record ↗

FDA Class I · Food · October 7, 2026

Coco G's Courmet Flaming Cheddar Hots recall — Coco G's Snack Foods, Inc.

Potential Salmonella contamination.

Company / brand: Coco G's Snack Foods recalls

Official ID H-1403-2026 · Official record ↗

FDA Class II · Food · October 7, 2026

Lior brand Cinnamon Ground Seasoning recall — Galil Importing Corp

Product contains elevated levels of lead.

Company / brand: Galil Importing recalls

Official ID H-1402-2026 · Official record ↗

FDA Class II · Food · October 7, 2026

Organiccs Absolutely Pure recall — Pacific Health Sciences Llc

Undeclared shellfish (crab shell): source of ingredient Glucosamine sulfate

Company / brand: Pacific Health Sciences recalls

Official ID H-1401-2026 · Official record ↗

FDA Class II · Food · October 7, 2026

Cloud Cafe branded Collagen Milk recall — TOJI CO.

Undeclared allergen ingredient (fish)

Company / brand: TOJI CO recalls

Official ID H-1400-2026 · Official record ↗

FDA Class II · Food · October 7, 2026

Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil recall — LMSI, LLC

Product contains garlic essential oil not approved for culinary use

Company / brand: LMSI recalls

Official ID H-1399-2026 · Official record ↗

FDA Class I · Food · October 7, 2026

Salata Salad Kitchen Jalapen¿o Avocado Dressing recall — Salata Dressings, LLC

This recall was initiated due to potential Salmonella contamination in diced jalape¿no received from the supplier

Company / brand: Salata Dressings recalls

Official ID H-1398-2026 · Official record ↗

FDA Class II · Food · October 7, 2026

7up Tropical beverage recall — Admiral Beverage Corporation

Product may contain undeclared sugar.

Company / brand: Admiral Beverage recalls

Official ID H-1397-2026 · Official record ↗

FDA Class II · Food · October 7, 2026

Khazana The Treasure Spice Magic Fennel Candy recall — SLT Foods Inc.

Undeclared Yellow 5 & 6, Red 3, and Blue 1

Company / brand: SLT Foods recalls

Official ID H-0001-2027 · Official record ↗

FDA Class II · Drug · October 7, 2026

Benzoyl Peroxide Wash recall — SV Labs Toronto Corporation

Microbial contamination of topical product.

Company / brand: SV Labs Toronto recalls

Official ID D-0879-2026 · Official record ↗

FDA Class II · Drug · October 7, 2026

Benzoyl Peroxide Wash recall — SV Labs Toronto Corporation

Microbial contamination of topical product.

Company / brand: SV Labs Toronto recalls

Official ID D-0878-2026 · Official record ↗

FDA Class II · Drug · October 7, 2026

Paroxetine Extended-Release Tablets recall — Apotex Corp.

Failed dissolution specifications.

Company / brand: Apotex recalls

Official ID D-0877-2026 · Official record ↗

FDA Class II · Drug · October 7, 2026

Buprenorphine Hydrochloride recall — Par Health USA, LLC

Crystallization

Company / brand: Par Health USA recalls

Official ID D-0876-2026 · Official record ↗

FDA Class II · Drug · October 7, 2026

Zoladex (goserelin) implant recall — TerSera Therapeutics LLC

Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.

Company / brand: TerSera Therapeutics recalls

Official ID D-0875-2026 · Official record ↗

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Government sources last checked October 22, 2026 at 12:00 PM UTC.