replacement available Recalls

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

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.

GOOT ESSA GOOT ESSA Sheep Tomme Style Cheese Recalled for Listeria Monocytogenes (2025)

The firm had a positive Listeria Monocytogenes on a sample from this batch of product made.

Gina Marie Bakery Cookies Recalled for Undeclared Red 40 and Yellow 6

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.

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.

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

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

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

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

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.

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

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.

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 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.

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.

Iantrek CycloPen CP-300 Cyclodialysis System Recalled for Sterile Packaging Integrity (2025)

Potential for compromised integrity of the sterile packaging.

Iantrek C-Rex UNO CRX-120 Goniotomy Instrument Recalled for Packaging Integrity Issue (2025)

Potential for compromised integrity of the sterile packaging.

Sandoz Cyclophosphamide Injection 500 mg/5 mL Recalled for Temperature Excursion During Transport

cGMP deviations: Temperature excursion during transportation.

Spacelabs Healthcare DVI Display Cables Recalled for EMI Risk in 16,898 Units (2025)

Philips Ultrasound OMNI II TEE Transducer Recall Two Units Nationwide (2025)

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.