infant product Recalls

Anderson Candy Company Recalls 960,000 Peanut Rounds for Undeclared Soy Allergen (2025)

Maquet Cardiovascular Heartstring III Proximal Seal System Recalled for 168 Units Worldwide (2025)

Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis.

Maquet Cardiovascular Recalls Heartstring III Proximal Seal System 3.8 mm Occluder (32,867 Units) 0

Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis.

Viewrail Recalls LED Control Module for Floating Stairs Over Fire Hazard

Synergy Housewares Recalls Wolfgang Puck Petite Tea Kettles for Burn Hazard (14 oz) Sold on HSN

Firefly Safe & Green 32 oz. Fuel Bottles Recalled for Poisoning Risk to Children

Empower Brands Recalls Remington Hair Dryers Over Electrocution Hazard (2025)

AquaStar Shrimp Recall: 22,500 Cases Recalled Over Cs-137 Contamination Risk (2025)

Product may be contaminated with Cesium-137 (Cs-137).

STWUQIKONG Three-Tier Spiral Tower Toy Recalled for Choking Hazard (2025)

This recall involves three-tiered spiral children's tower toys. The recalled toy has three levels and a basketball hoop with a character's face at the top. The toy measures about 10 inches high by 4 inches wide and came with three yellow balls.

Novartis/Sandoz Otic Suspension Recalled for Temperature Abuse (D-0626-2025)

Philips IQon Spectral CT 728332 Recalled Globally for Descending Patient Table Hazard

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Philips CT Systems Brilliance 40/64 Channel and Ingenuity Flex Recalled for Couch Descent Risk (2025

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Philips CT Systems Recalled for Descent Hazard In 210-Unit Worldwide Distribution (2025)

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Philips Ingenuity CT System Recall 2025: 285 Units Worldwide

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Beckman Coulter DxH 900 COULTER Hematology Analyzer Recalled for Inaccurate Hemoglobin Results

Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.

HEB Blueberry Yogurt Pretzels Recalled for Undeclared Wheat Allergen (2025)

Penner Patient Care Penner Pacific Bathing Spa Recalled for Missing UDI (25 Units, 2025)

The device does not bear a unique device identifier.

Penner Pacific Bathing Spa Recalled for Missing Unique Device Identifier (UDI) in 206 Units

The device does not bear a unique device identifier.

Penner Patient Care Bathing Spa Devices Recall for Missing Unique Device Identifier (Z-1500-2026)

The device does not bear a unique device identifier.

Penner Pacific Bathing Spa Recalled for Missing Unique Device Identifier in 190 US Units (2025-2026)

Penner Patient Care recalls 190 Bathing Spa devices nationwide after discovering the units lack a unique device identifier. The issue involves missing UDI on the device. Stop using the device immediately and follow the recall instructions.