replacement available Recalls

Black Sheep Egg Company Recalls 23,400 Dozen Free Range Grade AA Eggs Over Salmonella Risk (2025)

Ascend Laboratories Recalls Atorvastatin Calcium 80 mg Tablets (90-Count & 500-Count) for Failed Dil

Ascend Laboratories Recalls Alkem Atorvastatin Calcium 20 mg Tablets for Dissolution Failures (3 NDC

Kico Knee Innovation ARVIS Shoulder AI Planning Software Recalled for High-Risk Malalignment in 21-0

Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion.

Black Sheep Egg Company Recalls 46,800 Dozen Free Range Grade AA Eggs Over Salmonella Risk (2025)

Black Sheep Egg Company Recalls 23,400 Dozen Free Range Eggs Over Salmonella Risk (2025)

Black Sheep Egg Company Recall: 288,900 Dozen Free Range Grade AA Eggs Over Salmonella Risk

Beckman Coulter Recalls 160 DxC 500i Modules and DxI 9000 Analyzers in 2025 Recall

Black Sheep Egg Company Recalled 14,220 Dozen Free Range Eggs Over Salmonella Risk (2025)

Beckman Coulter Recalls 571 DxI 9000 Immunoassay Analyzers and DxC 500i (2025)

Black Sheep Egg Company Free Range Grade AA Eggs Recalled for Salmonella Risk (20,625 Dozen) 2025

Wuensche USA Recalls Ambiano Cotton Candy Makers 836098 Over Fire Hazard (2025)

Wuensche USA recalls Ambiano Cotton Candy Makers, model 836098, sold at ALDI. The recall cites a fire hazard from the heating element when the sugar receptacle is missing. Consumers should stop using the unit and pursue a refund.

Five Below Recalls Tabletop Fire Pits for Risk of Serious Burn Injury

Arizer Solo II Portable Vaporizers Recalled for Fire and Burn Hazards (Canada-Imported)

Arizer recalled the Solo II portable vaporizer on 2025-09-18 after reports of overheating lithium-ion batteries. The recall targets units imported by 7111495 Canada. Consumers should stop using the device and pursue a free replacement.

IcyBreeze Recall Expands Over Fire Hazard Risk in Portable Misting Fans (2025)

YooxArmor Recalled 2,000+ Kids’ Helmets Sold on Amazon Over Head-Injury Risk (2025)

Kirkland Signature Ahi Tuna Wasabi Poke Recalled Over Listeria Risk

Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke.

B Braun Medical Recalls 0 CE17TKFSDT Epidural Tray Kit for Lid Position Hazard (2025)

Potential for the lid of the catheter connector to be in the incorrect position.

GE Medical Systems LOGIQ P9 R4.5 Ultrasound System Recalled for Inaccurate Liver Readings (37 Units)

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

GE Medical Systems LOGIQ P10 Ultrasound System Recalled for UGAP Data Inaccuracy (31 Units, 2025)

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.