lithium battery Recalls

Hi-Tech Pharmaceuticals’ PrimeNutrition PhytoForm Fruits & Greens Recall for Unapproved Drug Claims

Unapproved Drug Claims and Misbranded.

Hi-Tech Pharmaceuticals Quercetin Dietary Supplement Recalled for Unapproved Drug Claims and Misbrnd

Unapproved Drug Claims and Misbranded.

Glenmark Carvedilol 12.5 mg Tablets Recalled for NNCI Impurity Exceeding FDA Limit (2025)

CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm

Olympus ViziShot 2FLEX Biopsy Device Recalled for Deformed Tips in 103,731 Units

Potential for undetected, deformed a-traumatic tips.

Hi-Tech Pharmaceuticals Joint-RX Dietary Supplement Recalled for Unapproved Drug Claims (2025)

Hi-Tech Pharmaceuticals PrimeNutrition Taurine Recall 85,950 Units in 2025

Unapproved Drug Claims and Misbranded.

Hi-Tech Pharmaceuticals Dietary Supplement LG Sciences Battle Hardener Platinum Series Recall for Un

Boston Scientific Encore 26 Inflation Device Recalled Over Foreign Particle Contamination

Haleon US Recall: Sensodyne PRONAMEL Active SHIELD Toothpaste Recalled for Label Mix-Up

Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is labelled Cool Mint/Whitening. The toothpaste inside the tube is Fresh Mint as indicated on the outer carton

Boston Scientific UroMax Ultra Kit MPNs Recalled Over Foreign Material Migration Risk (2025)

Hospira Sodium Bicarbonate Vial Recall for Sterility Concerns Affects 15,750 Vials

Lack of Assurance of Sterility.

Wasatch Photonics Raman Spectrometers Recall Expanded for Laser Safety Risks (2025)

DFA Dairy Brands Frozen Dessert Recalled for Undeclared Wheat and Soy, 324 Containers Affected

Product contains undeclared wheat and soy.

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.

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.

Quallent Duloxetine Delayed-Release Capsules 60 mg Recall Expanded for Impurity Above FDA Interim Lm

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Hyundai IONIQ 5 2025 Recall for High Voltage Battery Bus Bar Tightening Short Circuits (2025)

Hyundai Motor America (Hyundai) is recalling certain 2025 IONIQ 5 vehicles. The high voltage battery system may contain an improperly tightened bus bar, which can cause a short-circuit.

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

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

FENGQS F7 Pro Electric Bikes Recalled for Fire Hazards Sold on Amazon (2025)