All Product Recalls

Wegmans Grilling Camembert Recalled Due to Listeria Risk

Products may be contaminated with Listeria monocytogenes

Wegmans Camembert Cheese Recalled Due to Listeria Risk

Products may be contaminated with Listeria monocytogenes

Wegmans Brie Cheese Recalled Due to Listeria Risk

Wegmans Food Markets recalled 4,884 units of Caramel Apple Pecan Topped Brie Cheese on August 12, 2025. The cheese may be contaminated with Listeria monocytogenes, a serious pathogen. Consumers should not consume this product and seek a refund.

Applied Medical Technology Recalls NutraGlide ENFit Nasal Feeding Tube 5F-6F x 55 in (1,780 units)

Applied Medical Technology recalled 1,780 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. Distal tips on these devices may detach at lower than expected forces. Stop using immediately and follow the recall instructions.

Applied Medical Technology NutraGlide ENFit Nasal Feeding Tube Recall — 200 Units (2025)

The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

Applied Medical Technology NutraGlide ENFit Nasal Feeding Tube Recall 840 Units (2025)

The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

Applied Medical Technology NutraGlide ENFit Nasal Feeding Tubes Recalled for 390 Units in 2025

The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

Agilent Technologies Recalls 65 FLEX Monoclonal CD20 Antibodies Over Weak Staining Risk (GA60461-2CN

Their is the potential for weak staining which may result in false negative CD20 identification.

Agilent FLEX Monoclonal CD20 Antibody Recalled for 4,145 Units (2025)

Their is the potential for weak staining which may result in false negative CD20 identification.

Lannett Lisdexamfetamine Recall Alerts 40 mg Capsules for Label Mix-Up (2025)

Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.

Agilent Technologies Denmark ApS Recalls 67 FLEX CD20 Antibody for Potential Weak Staining

Their is the potential for weak staining which may result in false negative CD20 identification.

PHILIPS IntelliSpace Cardiovascular Software 8.0.0.4 Recall Affects 4 Units Nationwide

Software issue that results in the display of outdated information.

SUNGAL UDK Half Plum 170 g Recall for Cyclamate Adulteration (2025)

Baxter Continu-Flo Intravascular Set Recalled for Tubing Separation — 14,400 Units in 2025

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.

Glenmark Theophylline Extended-Release 400mg Recall Expanded for Failed Dissolution Tests (2025)

Quallent Pharmaceuticals Health LLC Recall Expands for Duloxetine Delayed-Release Capsules Over Imp-

CGMP deviations: N-nitroso-duloxetine impurity above the proposed interim limit.

Medline Medline Extremity Pack DYNJ45701B Sterile Kit Recall Affects 88 Units (2025)

Convenience kits labeled as sterile have not gone through the sterilization process.

Medline Industries Recalls 22 Sterile Convenience Kits DYNJ0382730O, DYNJ61038B (2025)

Convenience kits labeled as sterile have not gone through the sterilization process.

Schiller Argus PB-3000 Vital Signs Monitor Recall Affects 266 US Units

Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.

AliExpress Recalls LeymanKids Children's Pajama Sets for Burn Risk in 2025 Recall