All Product Recalls

Gina Marie Bakery Italian Sesame Cookies Recalled for Undeclared Sesame and Food Colorings (2025)

Undeclared Sesame, Undeclared Yellow 5, Red 40, Yellow 6

Gina Marie Bakery Recall: 172 Cases of Vanilla Chocolate Dipped Cookies Recalled for Undeclared Red

Gina Marie Bakery Biscotti Recalled for Undeclared Red 40

Gina Marie Bakery LLC recalled 172 cases of Toasted Almond & Cherry Biscotti after the FDA flagged undeclared Red 40. The recall is classified as high hazard. Consumers should avoid the product and contact the company for refunds or replacements.

Abbott TactiFlex Sensor Ablation Catheter Recall 2025 Affects 1,958 Units

Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.

Biomet Juggerknot Mini Soft Anchors 912080 Recall 40 Units Nationwide 2025

The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.

Hale Fresh Basil Infused Olive Oil Recall: 54 Bottles in Kentucky (2025)

Potential to be contaminated with Clostridium botulinum. Products manufactured without an approved process filed.

BioPro Recalls 147 Bipolar Heads Over Sterility Risk — Check Your Model Numbers

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

Hale recalls 54 bottles of Lotsa Pasta Roasted Garlic Infused Olive Oil for botulism risk (2025)

Potential to be contaminated with Clostridium botulinum. Products manufactured without an approved process filed.

MedicalCommunications GmbH Recalls 474 Ashvins HEYEX 2 / HEYEX PACS Software Units (2025)

Potential that the measured value may be smaller than the actual area.

BioPro Recalls 147 Metal and Ceramic Femoral Heads Over Sterility Packaging Issue

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

NOXBOX Recalled 1,667 NOxBOXi Nitric Oxide Delivery System Units in 2025

The unexpected internal fault / system diagnostic error to result when a rapid succession of button selections is made to the user interface without waiting for the device to respond to user prompts.

NOXBOX NOxBOXi Nitric Oxide Delivery System Recalled for 1,667 Units in 2025

Whole Foods Market Granola Recalled for Undeclared Allergens in 6-Unit Pack

Product was incorrectly labeled, resulting in undeclared wheat, sesame, and cashew.

Draeger Atlan A350 Anesthesia Workstations Recalled for Ventilator Failures in 2025

The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

BioPro Femoral Head Hip Implant Recall 147 Units in 2025 Texas and Michigan

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

Draeger Atlan A350XL Anesthesia Workstation Recalled for Ventilator Failure Risk (223 Units) in 25+N

The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

BioPro Endo Head Ceramic Recall Affects 147 Units Over Sterility Packaging Issue (2025)

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

Eureka Recalls Cinnamon for Elevated Lead Levels

Eureka recalled 32 cases of cinnamon on September 9, 2025, due to elevated lead levels. Consumers should not consume the product and seek refunds. The recall affects retail and wholesale customers in California and Michigan.

Lee K of NY Inc. Recalls 43-Unit Batch of PINOCCHIO CATERING Aged Kimchi Mackerel for Undeclared All

Product contains undeclared milk and shrimp

Beckman Coulter MicroScan Neg Multidrug Resistant MIC 1 C32368 Recall Expands Internationally (2025)

Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.