suffocation risk Recalls

Audi S5 Front Seat Belt Retractor Recall Affects 2025 VW Group Vehicles

Zydus Entacavir Recall 600 Bottles Over Impurity Degradation Issue (2025)

Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity

BD EpiCenter Recall: 2,050 Units Worldwide Over Unauthorized Access Risk

Biomet ZipTight AC Joint Implant Recall for 98 Units Over Missing Slotted Button (2025)

There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop

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.

LXDHSTRA Recall Expands on 2025 LXDHSTRA Baby Loungers and Crib Bumpers Sold on Amazon

EnHomee Fabric 13-Drawer Dressers Recalled for Tip-Over and Entrapment Risk (2025)

This recall involves EnHomee Fabric 13-Drawer Dressers. The Fabric 13-Drawer Dressers are 55.12" W x 35.45" H x 11.02" D and come in rustic brown, white, black, and pink.

Youbeien Crib Mobiles Recalled Due to Battery Ingestion Risk — Check Model RT668-17

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

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.

B Braun Medical ESPOCAN Spinal/Epidural Tray Recalled Over Lid Position Risk

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

B Braun Medical Recalls 2,840 Anesthesia Tray Kits Over Catheter Lid Defect (2025)

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

Cardinal Health 200 Salem Sump Gastroduodenal Tubes Recalled Worldwide for ARV Breakage

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

B Braun Medical Perifix FX Epidural Tray Recall for Lid Misalignment in Catheter Connector

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

Taproom Gourmet Bulk Fifth Avenue Mix Recalled for No Ingredient Label and Allergens

No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashew, and soy)

Taproom Gourmet Bulk Broadway Mix Recalled for Undeclared Allergens in 15lb Bulk Bags (2025)

No ingredient label. Product contains undeclared allergens (peanuts, sesame, wheat, and soy)

Cardinal Health 200 Salem Sump Stomach Tubes Recalled Worldwide in 2025 for ARV Breakage

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

Cardinal Health 200 Recalls Salem Sump Dual-Lumen Stomach Tubes Over ARV Breakage (2025)

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

B. Braun Medical Recalls 5,770 PERIFIX FX Epidural Anesthesia Trays for Lid Position Issue

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

B Braun Medical Recall Expands for Perifix FX Epidural Tray and Catheter Over Lid Position Defect (Z

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