Health & Personal Care
HIGH
FDA DEVICE
Microbiologics Recalls LYFO DISK Due to Testing Failure Risk
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
Microbiologics
Affected units
Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
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Food & Beverages
HIGH
FDA FOOD
Wegmans Recalls Deluxe Mixed Nuts Over Salmonella Risk
Wegmans recalled 3,024 units of Deluxe Mixed Nuts on December 2, 2025. The recall stems from potential Salmonella contamination. Consumers should not consume the product and seek refunds immediately.
Mellace Family Brands California
Potential contamination
Health & Personal Care
HIGH
FDA DEVICE
Microbiologics Recalls KWIK-STIK Kits Over Microorganism Recovery Failure
Microbiologics recalled 18 units of KWIK-STIK 6-Pack on December 2, 2025. The kits may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni. Patients and healthcare providers should stop using the device immediately.
Microbiologics
Affected units
Health & Personal Care
HIGH
FDA DEVICE
Zimmer Recalls Affixus Femoral Nailing System Over Fracture Risk
Zimmer recalled 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized distal diameter, risking fatigue fractures. This can lead to serious health complications requiring surgical intervention.
Zimmer
Affected implants
Health & Personal Care
HIGH
FDA DEVICE
Microbiologics Recalls KWIK-STIK Over Testing Failure Risk
Microbiologics recalled 86 units of the KWIK-STIK 2-Pack on December 2, 2025. The affected products may fail to recover the target microorganism Campylobacter jejuni. This recall affects units distributed worldwide, including the U.S.
Microbiologics
Affected units
Health & Personal Care
HIGH
FDA DEVICE
BD Catheter Recalled Due to Incorrect Expiration Labeling
BD recalled 149,310 hydrophilic catheters due to a labeling error regarding expiration dates. The recall affects the 14 Fr (4.7 mm) straight tip model, REF: RTU14F. Healthcare providers and patients must stop using the product immediately.
HANGZHOU BEVER MEDICAL DEVICES CO.
Labeling error,
Health & Personal Care
HIGH
FDA DEVICE
RayStation Radiation Therapy Software Recalled Over Dose Calculation Issue
RaySearch Laboratories AB recalled RayStation software on November 28, 2025, due to a malfunction. The software fails to invalidate calculated radiation doses for certain Regions of Interest. This defect poses a potential risk to patient safety.
RAYSEARCH LABORATORIES AB
Potential for
Health & Personal Care
HIGH
FDA DEVICE
RayStation Recalls Radiation Therapy System Over Dose Calculation Flaw
RAYSEARCH LABORATORIES AB
Potential for
Health & Personal Care
HIGH
FDA DEVICE
RaySearch Laboratories Recalls RayStation Software for Dose Calculation Error
RAYSEARCH LABORATORIES AB
Potential for
Health & Personal Care
HIGH
FDA DEVICE
RaySearch Laboratories Recalls RayStation Software Over Dose Calculation Error
RAYSEARCH LABORATORIES AB
Potential for
Health & Personal Care
HIGH
FDA DEVICE
RaySearch Laboratories Recalls RayStation Software Over Dose Calculation Error
RAYSEARCH LABORATORIES AB
Potential for
Health & Personal Care
HIGH
FDA DEVICE
RaySearch Laboratories Recalling Radiation Therapy Software Due to Safety Risk
RAYSEARCH LABORATORIES AB
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare Recalls SIGMA Spectrum Infusion Pump Over Infusion Risk
Baxter Healthcare
Certain pumps
Food & Beverages
HIGH
FDA FOOD
Mondelez Recalls Ritz Peanut Butter Crackers Over Allergen Risk
Mondelez Global recalled 70 cases of Ritz Peanut Butter Cracker Sandwiches on November 28, 2025. The recall stems from undeclared peanut allergens due to mispackaging. The affected product was distributed in eight states including Alabama and New York.
Mondelez Global
Undeclared allergens
Health & Personal Care
HIGH
FDA DEVICE
RaySearch Laboratories Recalls Radiation Therapy Software Over Dose Calculation Error
RAYSEARCH LABORATORIES AB
Potential for
Health & Personal Care
HIGH
FDA DEVICE
RaySearch Laboratories Recalls Radiation Therapy Software Due to High Risk
RAYSEARCH LABORATORIES AB
Potential for
Health & Personal Care
HIGH
FDA DEVICE
RaySearch Laboratories Recalls Radiation Therapy Software Due to Dose Calculation Error
RAYSEARCH LABORATORIES AB
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Advanced Bionics Sky CI M90 Recall: 2 Units Over Packaging Label Mismatch (2025)
Advanced Bionics recalled 2 Sky CI M90 behind-the-ear sound processors on 2025-11-27. The packaging label does not match the included product. Consumers should stop using the device and follow manufacturer instructions.
Advanced Bionics
Behind-the-ear sound
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls IV Administration Sets Due to Valve Issues
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
Medline Industries, LP
Medline kits
HIGH
CPSC
KingPavonini Recalls 6 Adult Portable Bed Rails Over Entrapment Risk (2025 Recall)
KingPavonini
The recalled