Latest recalls — page 24

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

3,525 recalls in our current data. Showing 2,301–2,400, newest first.

FDA Class II · Medical device · June 17, 2026

NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 recall — In2bones USA, LLC

Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.

Company / brand: In2bones USA recalls

Official ID Z-2355-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

DigitalDiagnost C90 Flex/Value/Chest/ER recall — Philips North America Llc

System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

Company / brand: Philips North America recalls

Official ID Z-2354-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

SD LTM 64 PLUS recall — Micromed S.p.A.

Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple amplifier configuratio…

Company / brand: Micromed S.p.A recalls

Official ID Z-2353-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2352-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2351-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2350-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2349-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2348-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2347-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2346-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2345-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2344-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2343-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2342-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2341-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2340-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2339-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2338-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2337-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2336-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2335-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2334-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2333-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — HF Acquisition Co LLC

Due to incorrect incubation process being performed on product.

Company / brand: HF Acquisition Co recalls

Official ID Z-2332-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — HF Acquisition Co LLC

Due to incorrect incubation process being performed on product.

Company / brand: HF Acquisition Co recalls

Official ID Z-2331-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

CGuard¿ Prime Carotid Stent System recall — INSPIREMD Inc

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Company / brand: INSPIREMD recalls

Official ID Z-2330-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

CGuard Prime Carotid Stent System recall — INSPIREMD Inc

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Company / brand: INSPIREMD recalls

Official ID Z-2329-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — INSPIREMD Inc

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Company / brand: INSPIREMD recalls

Official ID Z-2328-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

CGuard Prime Carotid Stent System recall — INSPIREMD Inc

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Company / brand: INSPIREMD recalls

Official ID Z-2327-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — INSPIREMD Inc

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Company / brand: INSPIREMD recalls

Official ID Z-2326-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — INSPIREMD Inc

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Company / brand: INSPIREMD recalls

Official ID Z-2325-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

TDC VELOCE" recall — D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls

Official ID Z-2324-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

TDC VELOCE" recall — D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls

Official ID Z-2323-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

TDC VELOCE" recall — D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls

Official ID Z-2322-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Bicarby" Dialysate recall — Fresenius Medical Care Holdings, Inc.

Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-…

Company / brand: Fresenius Medical Care Holdings recalls

Official ID Z-2321-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves recall — BERLIN HEART GMBH

Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.

Company / brand: BERLIN HEART recalls

Official ID Z-2320-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Mahurkar Elite PASS Trays recall — Mozarc Medical US LLC

The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.

Company / brand: Mozarc Medical US recalls

Official ID Z-2319-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia Moveo angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Company / brand: GE Medical Systems recalls

Official ID Z-2318-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia IGS Pulse angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Company / brand: GE Medical Systems recalls

Official ID Z-2317-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia IGS 7 Pulse angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Company / brand: GE Medical Systems recalls

Official ID Z-2316-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia IGS 5 Pulse angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Company / brand: GE Medical Systems recalls

Official ID Z-2315-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Allia IGS 3 Pulse angiographic X-ray system recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…

Company / brand: GE Medical Systems recalls

Official ID Z-2314-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Plum Duo Precision IV Pump recall — ICU Medical, Inc.

Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…

Company / brand: ICU Medical recalls

Official ID Z-2313-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Plum Duo Infusion Pump recall — ICU Medical, Inc.

Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…

Company / brand: ICU Medical recalls

Official ID Z-2312-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Plum Solo Precision IV Pump recall — ICU Medical, Inc.

Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…

Company / brand: ICU Medical recalls

Official ID Z-2311-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Fresh Roast Systems ColorTrack recall — Fresh Roast Systems Inc

A defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which could under very rare specific misuse circumstances …

Company / brand: Fresh Roast Systems recalls

Official ID Z-2280-2026 · Official record ↗

FDA Class II · Food · June 17, 2026