replacement available Recalls

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.

Ortoma AB Recalls 261 Inserter Adapters for Hip Cup Tools (2025)

Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.

Kia K5 2023-2025 Recall for Loose Rear Window Trim Pieces in 2025

Kia America, Inc. (Kia) is recalling certain 2023-2025 K5 vehicles. The left and right rear window trim pieces may loosen and detach.

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.

Kia Telluride Exterior Trim Recall for 2023-2025 Models (2027 Recall)

Kia America, Inc. (Kia) is recalling certain 2023-2025 Telluride vehicles. The door belt molding trim can delaminate and detach from the vehicle.

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.

Medline Recalls 596 Flexicare BritePro Solo Fiber Optic Laryngoscope Handles in 2025

Medline Industries, LP recalled 596 Medline kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light may fail to illuminate as designed. Healthcare providers should stop using the devices immediately and follow recall instructions.

Ford 2025 Expedition Recalled for Brake Software Issue; OTA Update Available

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.

BMW Recalls 2025 Motorcycles Over eCall Crash Notification Risk

BMW recalls 2025 motorcycles with optional eCall system due to a software error that can deactivate emergency crash notification. OTA or dealer update will fix the issue. Letters to owners go out Sept. 12, 2025. Contact BMW at 1-800-525-7417.

Home Health US Recalled 4,661 One Step Sterile Lancets for Single Use (2025)

Due to incorrect/lack of Unique Device Identifier (UDI) codes.

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

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.

iMirror Recalls Electric Bug Zapper Racket, Fly Swatter and Mosquito Swatter (2025)

This recall involves the Electric Bug Zapper Racket, Fly Swatter and Mosquito Swatter for indoor and outdoor use. There is a rectangular silver sticker displaying model number BZ-001 on the back of the electric mosquito swatter handle.

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

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.

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

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

Curtis International Recalls Frigidaire Mini Fridges After Fire Hazard (2025)