immediate action Recalls

Zimmer Recalls Affixus Antegrade Femoral Nails Over Fracture Risk

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.

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.

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.

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.

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.

RaySearch Laboratories Recalls RayStation Software Over Dose Calculation Error

Baxter Healthcare Recalls SIGMA Spectrum Infusion Pump Over Infusion Risk

RaySearch Laboratories Recalling Radiation Therapy Software Due to Safety Risk

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.

RayStation Recalls Radiation Therapy System Over Dose Calculation Flaw

RaySearch Laboratories Recalls RayStation Software for Dose Calculation Error

RaySearch Laboratories Recalls RayStation Software Over Dose Calculation Error

RaySearch Laboratories Recalls Radiation Therapy Software Over Dose Calculation Error

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.

RaySearch Laboratories Recalls Radiation Therapy Software Due to High Risk

RaySearch Laboratories Recalls Radiation Therapy Software Due to Dose Calculation Error

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.

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.

Ebern Designs Ojaswi 12-Drawer Dressers Recalled for Tip-Over Risk (2025)