lithium battery Recalls

262 recalls tagged with “lithium battery”.

Health & Personal Care
HIGH
FDA DEVICE

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

Olympus Corp of the Americas recalled 103,731 ViziShot 2FLEX single-use aspiration needles worldwide after officials flagged potential undetected, deformed atraumatic tips. The recall covers the NA-U403SX-4019 model. Healthcare providers must halt use immediately and follow manufacturer instructions for recall. Manufacturers say notification was by letter.

Olympus Corporation of the Americas
Potential for
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Health & Personal Care
HIGH
FDA FOOD

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

Hi-Tech Pharmaceuticals recalled 85,950 units of the LG Sciences Battle Hardener Platinum Series Complete 6 Week Cycle dietary supplement due to unapproved drug claims. The recall targets states across the U.S. The company is listed as Hi-Tech Pharmaceuticals. The remedy is a refund or replacement after notification by letter.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Health & Personal Care
HIGH
FDA FOOD

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

Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition Taurine Mental & Athletic Performance dietary supplement distributed nationwide. The FDA enforcement report cites unapproved drug claims and misbranding. Consumers who purchased this product should not consume it and should contact the company for refund or replacement.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Health & Personal Care
HIGH
FDA DRUG

Westminster Pharmaceuticals Metoprolol Tartrate 50 mg Recall Over Nitrosamine Above ADI Level (2025)

Westminster Pharmaceuticals recalls 16,672 boxes of Metoprolol Tartrate 50 mg tablets nationwide after nitrosamine exceeds Acceptable Daily Intake. Manufactured by Renata PLC in Bangladesh and distributed in the US by Westminster Pharmaceuticals. Consumers should stop using the product and contact their healthcare provider for guidance.

METOPROLOL TARTRATE
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

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

Glenmark Pharmaceuticals Inc., USA recalls 17,496 bottles of Carvedilol tablets sold nationwide after NNCI impurity exceeded FDA limits. The recall covers lot numbers 17241257, 17241258, and 17241279 with Exp. Date 06/2026. Consumers should stop using the product and contact Glenmark or their healthcare provider for guidance.

Glenmark Pharmaceuticals Inc.
CGMP Deviations:
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Health & Personal Care
HIGH
FDA FOOD

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

Hi-Tech Pharmaceuticals recalled 85,950 units of its Quercetin dietary supplement distributed to 40+ states after FDA enforcement found unapproved drug claims and misbranding. The recall, active as of Aug 6, 2025, stems from regulatory concerns rather than a reported health incident. Consumers should stop using the product and contact the company for refunds or replacements.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Food & Beverages
HIGH
FDA FOOD

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

Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition PhytoForm Fruits & Greens Formula after FDA enforcement flagged unapproved drug claims and misbranding. The dietary supplement was distributed to 40+ states before the recall was issued on 2025-08-06 and remains active. Consumers should not consume the product and should seek refund or replacement from Hi-Tech Pharmaceuticals.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Encore 26 Inflation Device Recalled Over Foreign Particle Contamination

Boston Scientific recalls 39,739 Encore 26 Inflation Devices worldwide after an internal investigation found foreign material particles could migrate from the device into balloon dilation catheters. The high-severity recall affects interventional cardiology and peripheral interventions devices. Stop using immediately and await recall instructions from Boston Scientific or healthcare providers.

Boston Scientific
The Encore
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Health & Personal Care
HIGH
FDA DEVICE

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

Boston Scientific recalled 1,369 Encore 26 Inflation Devices used with balloon dilation catheters after an internal investigation found foreign material particles could migrate into a balloon dilatation catheter. The recall affects 12 UPNs including M0062251200 through M0062251370. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.

Boston Scientific
The Encore
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Health & Personal Care
HIGH
FDA DEVICE

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

Wasatch Photonics recalled 192 Raman spectrometers in the United States after identifying two potential laser safety failure modes. Models 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC, and 785-ER-ILC are included. The defect could occur under excessive force or extreme continuous vibration. Stop using immediately and follow the manufacturer’s recall instructions.

WASATCH PHOTONICS
Two new
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Health & Personal Care
HIGH
FDA DEVICE

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

Fortress Introducer Sheath System recalled 2,500 units linked to label mispackaging. The devices were distributed worldwide, including 15 U.S. states and numerous international markets. The incorrect pouch label lists the 4F version reference and unique device identifier instead of the packaged 6F version. Healthcare providers must stop use and follow manufacturer recall instructions.

Fortress Introducer Sheath System
Units may
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Health & Personal Care
HIGH
FDA DRUG

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

Quallent Pharmaceuticals Health LLC recalls 1,856 bottles of Duloxetine delayed-release capsules due to CGMP deviations and an impurity above FDA interim limits. The recall is active as of August 20, 2025. Patients and providers should stop use and contact Breckenridge Pharmaceutical or a healthcare provider for guidance.

DULOXETINE
CGMP Deviations:
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Tag Statistics

Total Recalls
262

Related Tags

electrical hazardchemical hazardimmediate actionstop use immediatelyreplacement availablefda regulatedcpsc regulatedtoddler productinfant productadult productelectronicbattery powered
    lithium battery Recalls | RecallRadar