infant product Recalls

Medline Recalled 7,913 Reprocessed ACUSON AcuNav Ultrasound Catheters for Intracardiac Imaging

Medline Recalled 7,913 Reprocessed Webster CS Catheters for Electrophysiology Mapping

Medline Reprocesses 7,913 Electrophysiology Catheters for Safety Risks

Exela Pharma Sciences 4.2% Sodium Bicarbonate Injection Recalled Over Arsenic Impurity Out-Of-Spec

Failed Impurities/Degradation Specifications: out of specification results for arsenic in the impurities tested.

Fortress Introducer Sheath System 386594 Recall Expanded; 2,500 Units Worldwide Distribution (High-R

Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version.

Ortho-Clinical Diagnostics LAC Slides Recalled Over Calibration Failures on VITROS Systems

Pfizer Levoxyl Recall: Subpotent Levoxyl 50 mcg Tablets, 29,004 Bottles in U.S. Market (2025)

Pfizer's Levoxyl 50 mcg levothyroxine tablets are recalled due to subpotency. About 29,004 bottles distributed in the U.S. since distribution. Consumers should stop use and contact their healthcare provider for guidance.

Dynamic Sports Nutrition Recall: WINN-50 Vanazolol Dietary Supplement Sub-Potent for Vitamin B12 (H-

Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims.

Medline Recalls 2,520 Kits With Flexicare Laryngoscope Handles Over Lighting Failure (2025)

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.

Zap Surgical Systems ZAP-X Radiosurgery System Recalled for 17 Units Worldwide in 2025

Innovative Designs Recalls Minecraft Light-Up Slap Ruler Bracelets (2025)

Transpro US Recalls Electric Scooters for Unauthorized Battery Labels, Fire Risk

Cipla USA Albuterol Sulfate Inhalation Aerosol Recall Expanded for Stability Variance (2025)

Failed Stability Specifications: Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the 12-month time point.

Pura Scents Recalls Pura 4 Smart Home Diffuser Covers Over Magnet Ingestion Hazard (2025)

LIVACTI LT-BG01-3 Retractable Safety Gates Recalled for Entrapment Risk (2025)

Minongad LED Gloves ST01 Recalled for Battery Ingestion Hazard Sold on Amazon (2025)

Diamond G Forest Products Recalled 4-Ounce Turpentine Bottles for Child-Resistant Packaging Violate

This recall involves 100% pure gum spirits of turpentine bottles. The 4-ounce, clear glass bottles are round and have a label with "Georgia Pine Gum Spirits of Turpentine" and "Diamond G Forest Products" printed on it.

Taizhou Kangping Medical 3.85 Million Cartons of BZK Antiseptic Towelettes Recalled for Sterility LQ

Lack of Assurance of Sterility.

Bestway, Intex and Polygroup Recall 48-Inch+ Above-Ground Pools Over Drowning Hazard (2025)

Ascend Laboratories Amlodipine and Olmesartan Medoxomil Recall for Low Dissolution 8,568 Bottles in

Failed Dissolution Specifications: low dissolution results