Fresh Recalls

Latest recalls — page 6

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

3,525 recalls in our current data. Showing 501–600, newest first.

FDA Class II · Medical device · September 23, 2026

Brand Name recall — PTW FREIBURG

When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead users to incorr…

Company / brand: PTW FREIBURG recalls

Official ID Z-3174-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

GM Helix Implant recall — Straumann USA LLC

There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.

Company / brand: Straumann USA recalls

Official ID Z-3173-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

SunMed Tracheal Tube recall — WELL LEAD MEDICAL CO. LTD

The 6Fr suction catheter could not pass through the samples smoothly.

Company / brand: WELL LEAD MEDICAL CO recalls

Official ID Z-3172-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Core Services Hub V8 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3171-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Workflow Core Services V8 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3170-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Centricity PACS Server V7 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3169-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Centricity PACS V2 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3168-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Enterprise Archive V8 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3167-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Centricity Enterprise Archive V2 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3166-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

NOxBOXi Nitric Oxide Delivery System recall — NOXBOX LTD

Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation.

Company / brand: NOXBOX recalls

Official ID Z-3165-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Brand Name recall — Nuclein LLC

Due to a software issue

Company / brand: Nuclein recalls

Official ID Z-3164-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3163-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3162-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3161-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3160-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Oncology sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3159-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Oncology sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3158-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Non-Dedicated Gravity Administration Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3157-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Plum administration sets recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3156-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Haylard UNIV IMAGING BIOPSY TRUCUSTOM recall — AVID Medical, Inc.

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Company / brand: AVID Medical recalls

Official ID Z-3154-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Haylard BASIC BIOPSY TRAY recall — AVID Medical, Inc.

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Company / brand: AVID Medical recalls

Official ID Z-3153-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Haylard CONTINUOUS NERVE BLOCK TRAY recall — AVID Medical, Inc.

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Company / brand: AVID Medical recalls

Official ID Z-3152-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Haylard 18G SINGLE SHOT EPI TRAY recall — AVID Medical, Inc.

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Company / brand: AVID Medical recalls

Official ID Z-3151-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Impella Optical Controller recall — Abiomed, Inc.

The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.

Company / brand: Abiomed recalls

Official ID Z-3150-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Impella Optical Controller with the below product descriptions and corresponding Product C recall — Abiomed, Inc.

The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.

Company / brand: Abiomed recalls

Official ID Z-3149-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Automated Impella Controller (AIC) with the below product descriptions and corresponding P recall — Abiomed, Inc.

The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.

Company / brand: Abiomed recalls

Official ID Z-3148-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System recall — Bayer Medical Care, Inc.

Some devices may not have been properly sterilized due to a manufacturing sterilization issue.

Company / brand: Bayer Medical Care recalls

Official ID Z-3147-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Percutaneous Insertion Kit (PIK) recall — Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

Company / brand: Maquet Cardiopulmonary recalls

Official ID Z-3146-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Percutaneous Insertion Kit (PIK) recall — Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

Company / brand: Maquet Cardiopulmonary recalls

Official ID Z-3145-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Percutaneous Insertion Kit (PIK) recall — Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

Company / brand: Maquet Cardiopulmonary recalls

Official ID Z-3144-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 recall — GE Medical Systems Information Technologies Inc

Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.

Company / brand: GE Medical Systems Information Technologies recalls

Official ID Z-3143-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Philips PIC iX Essentials REF recall — Philips North America

Due to software malfunction, patient information system may freeze and become unresponsive.

Company / brand: Philips North America recalls

Official ID Z-3142-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Philips Patient Information Center iX REF recall — Philips North America

Due to software malfunction, patient information system may freeze and become unresponsive.

Company / brand: Philips North America recalls

Official ID Z-3141-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Medline Convenience Kit recall — Medline Industries, LP

The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a comprom…

Company / brand: Medline Industries recalls

Official ID Z-3137-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose and B- Ketone meter recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3132-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose and B- Ketone meter recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3131-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose and B- Ketone meter recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3130-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose Hospital Meter System recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3129-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose Hospital Meter System recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3128-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3127-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3126-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3125-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3124-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3123-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3122-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3121-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Halyard IV START KIT NON-STERILE REF recall — AVID Medical, Inc.

Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides

Company / brand: AVID Medical recalls

Official ID Z-3108-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusi recall — BD SWITZERLAND SARL

Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.

Company / brand: BD SWITZERLAND SARL recalls

Official ID Z-3080-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

DuoGlide Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.

this is a downstream recall of class I recall RES 98777

Company / brand: Bard Access Systems recalls

Official ID Z-2985-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.

this is a downstream recall of class I recall RES 98777

Company / brand: Bard Access Systems recalls

Official ID Z-2984-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Mon Sire Brie recall — Optimus Inc. d/b/a/ Markys Caviar

The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.

Company / brand: Optimus d/b/a/ Markys Caviar recalls

Official ID H-1388-2026 · Official record ↗

FDA Class III · Food · September 23, 2026

Hexing Haw Balls candy recall — Tiffany Food Corp

Unapproved dye Ponceau 4R

Company / brand: Tiffany Food recalls

Official ID H-1387-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

PUMPKIN SPICE NO BAKE COOKIE NET WT 3 recall — Best Friends Bakery, LLC

Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no …

Company / brand: Best Friends Bakery recalls

Official ID H-1386-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Elegant Foods Carrot Cake recall — Elegant Foods, LLC

Carrot decoration contains Yellow #5 and Yellow #6 which is not listed on finished product label.

Company / brand: Elegant Foods recalls

Official ID H-1385-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Elegant Foods Golden Raisins recall — Elegant Foods, LLC

Undeclared sulfites

Company / brand: Elegant Foods recalls

Official ID H-1384-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Elegant Foods Coconut Flakes recall — Elegant Foods, LLC

Undeclared sulfites

Company / brand: Elegant Foods recalls

Official ID H-1383-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Buckhead recall — Buckhead Meat Company D.B.A. Trinity Seafood

The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.

Company / brand: Buckhead Meat Company D.B.A. Trinity Seafood recalls

Official ID H-1382-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Organic Triple Berry Blend Strawberries recall — Frutas y Hortalizas del Sur S.A.

Potential E. coli O145:H28 Contamination

Company / brand: Frutas y Hortalizas del Sur recalls

Official ID H-1380-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

PICO DE GALLO-HOT-6/9oz HEB-PICO-HOT-12/14oz recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1379-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

HEB-PICO-MEDIUM-12/14oz PICO DE GALLO-MEDIUM-6/14oz PICO DE GALLO-MEDIUM-6/9oz PICO-DE-GAL recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1378-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

HEB-GUAC KIT-MILD-3/57 recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1377-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

NatureBest Mild Cheddar & Jalapeno Stuffed Mushrooms 8oz (227g) HEB SI JAL POP STFFD MUSHR recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1376-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

PEPPER-JALAPENO-DC 1/4"-4/5# PEPPER-JALAPENO-DC 1/4"-1/5# PEPPER-JALAPENO-SL 1/8"-1/5# PEP recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1375-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

HEB-PICO-MANGO-12/14oz PICO DE GALLO-MANGO-4/14oz PICO DE GALLO-MANGO-6/14oz recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1374-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

SOUP MIX-6/58oz Tray recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1373-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

PICO DE GALLO-MILD-4oz PICO DE GALLO-MILD-6/14oz PICO DE GALLO-4/5# PICO DE GALLO-1/5# PIC recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1372-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

BH Bold Chef Salad Kit recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1368-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1367-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Fresh Pico Tray recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1366-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo Hot recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1365-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Tomato Salsa Fresca recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1364-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Salsa Fresca Medium recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1363-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Salsa Verde Mild recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1362-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Salsa Roja Medium recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1361-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo Spicy recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1360-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo Mild recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1359-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Hot Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1358-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Mild Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1357-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1356-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1355-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pineapple Mango Salsa Mild recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1354-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Mango Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1353-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Authentic Guacamole recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1352-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Spicy Guacamole recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1351-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Fiesta Salad with Shrimp recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1350-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Taco Dip recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1349-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Spicy Pimento Cheese Dip recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1348-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Spicy Jalapeno Jarlsberg Dip recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1347-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Spicy Roast Beef Sandwich (closed-face) recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1346-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Rice & Bean Burrito recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1345-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Diced Jalapenos recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1344-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Mercer's brand 6 ICE CREAM SANDWICHES TO GO recall — Quality Dairy Farms Inc.

Undeclared peanuts

Company / brand: Quality Dairy Farms recalls

Official ID H-1343-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Martina brand Fresh Whole Mangoes recall — Panorama Produce Sales Inc.

Product may be contaminated with Salmonella

Company / brand: Panorama Produce Sales recalls

Official ID H-1342-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Everything Sprouts Robust Radish Mix recall — Everything Sprouts, LLC

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

Company / brand: Everything Sprouts recalls

Official ID H-1340-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Everything Sprouts Crunchy Protein Sprout Mix recall — Everything Sprouts, LLC

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

Company / brand: Everything Sprouts recalls

Official ID H-1339-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Everything Sprouts Zesty Garlic Mix recall — Everything Sprouts, LLC

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

Company / brand: Everything Sprouts recalls

Official ID H-1338-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Everything Sprouts and Calco branded Alfalfa Sprouts recall — Everything Sprouts, LLC

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

Company / brand: Everything Sprouts recalls

Official ID H-1337-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Foods Alive organic moringa leaf powder recall — FOODS ALIVE INC.

Potential Salmonella contamination

Company / brand: FOODS ALIVE recalls

Official ID H-1336-2026 · Official record ↗

FDA Class I · Drug · September 23, 2026

Thyroid Tablets recall — VITRUVIAS THERAPEUTICS INC

Superpotent Drug

Company / brand: VITRUVIAS THERAPEUTICS recalls

Official ID D-0866-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Dopamine HCl Inj recall — Pfizer

Lack of Assurance of Sterility

Company / brand: Pfizer recalls

Official ID D-0853-2026 · Official record ↗

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