lithium battery Recalls

262 recalls tagged with “lithium battery”.

Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems AW Server 2.0, AW Server 3.0, 3.1, 3.2 Recalled For Security Breach Risk (2025)

GE Medical Systems recalled 7,302 AW Server models worldwide, including 1,381 units in the U.S., after identifying a security vulnerability that could expose patient data. The defect could allow a malicious actor to compromise confidentiality, integrity and availability of information. Healthcare providers should stop using the devices immediately and follow manufacturer instructions for recall.

GE Medical Systems
Firm has
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Recalled AR-15 Chamber Lock Pro (Red)
HIGH
CPSC

StopBox USA Recalls AR-15 Chamber Lock Pro for Risk of Serious Injury or Death

StopBox USA recalls AR-15 Chamber Lock Pro shipped June 2 to July 15, 2025. The recall covers locks designed to chamber-lock AR-15 style rifles. The defect allows the lock to be forcibly removed, enabling unauthorized access to the firearm. StopBox urges immediate stop-use and provides refunds or replacements.

StopBox USA
A manufacturing
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Food & Beverages
HIGH
FDA FOOD

Gospodarstwo Pasieczne Sadecki Bartnik Bee Pollen 200g Recall for Pyrrolizidine Alkaloids (2025)

Gospodarstwo Pasieczne Sadecki Bartnik recalled 336 jars of Bee Pollen sold in Illinois after tests detected pyrrolizidine alkaloids. The product contains detectable pyrrolizidine alkaloids. Consumers should not consume the product and should contact the producer by telephone for refund or replacement.

Gospodarstwo Pasieczne Sadecki Bartnik
detectable pyrrolizidine
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems High-Rire Recall: 32,433 Medical Convenience Kits Recalled for Re-GassedEO

American Contract Systems recalled 32,433 medical convenience kits nationwide after finding re-gassed devices from EO sterilization. The recall affects five product lines with UDI-DI codes and Lot numbers. The re-gassing process has not been validated for multiple sterilization cycles, calling into question product safety and effectiveness. Health providers and patients should stop using these kit

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/20 Recall Affects 75 Systems Worldwide for Internal Component Deterioration

Philips Medical Systems Nederland B.V. recalls 75 Allura Xper FD20/20 imaging systems due to potential deterioration of the CMOS battery, hard drive and power supply. Motorized movements could become unavailable while X-ray imaging remains functional. Operators should stop using affected units and follow manufacturer instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
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Health & Personal Care
HIGH
FDA DRUG

Zydus Lifesciences Chlorpromazine Hydrochloride Tablets 50 mg 100-count Recall 2025

Zydus Lifesciences and Northstar Rx LLC recall Chlorpromazine Hydrochloride Tablets, 50 mg, 100-count bottles distributed nationwide in the United States. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above the acceptable intake limit. Stop using the product immediately and contact your healthcare provider or Zydus Pharmaceuticals (USA) Inc for guidance.

Zydus Lifesciences
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Philips Philips Medical Systems Netherlands B.V. Allura Xper FD20/20 OR Table Recall Affects 3 Units

Philips Medical Systems Netherlands B.V. recalled 3 Allura Xper FD20/20 OR Tables worldwide, including the US, on 2025-09-03 after detection of degradation in internal components. The recall cites CMOS battery, hard disk drive, and/or power supply unit deterioration. Motorized movements may fail while imaging remains available. The recall is active. Stop using the device following recall guidance.

Philips Medical Systems Netherlands B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD10 Recall 2025: 1,117 Imaging Systems Worldwide Face Movement-Dysfunction Risk

Philips Medical Systems Netherlands B.V. recalls 1,117 Allura Xper FD10 imaging systems worldwide, including 252 units in the United States. The defect involves deterioration of internal components such as the CMOS battery, hard disk drive and power supply unit, which can disable motorized movements. Hospitals should stop using the devices and follow the manufacturer recall instructions.

Philips
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/10 Recall 45 Units Worldwide in 2025

Philips Medical Systems Nederland B.V. recalls 45 Allura Xper FD20/10 imaging systems worldwide due to internal component deterioration. The CMOS battery, hard disk drive and/or power supply may fail. Motorized movements can become unavailable while imaging remains possible. Stop using the device and follow manufacturer instructions.

Philips Medical Systems Nederland B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Nederland B.V. Recalled 98 Imaging Systems for CMOS Battery, HDD, PSU Deteri

Philips Medical Systems Nederland B.V. recalls 98 imaging systems worldwide after reports of component deterioration. Systems may lose motorized movements due to CMOS battery, hard disk drive, or power supply deterioration. Imaging remains available. Stop using the device and follow manufacturer instructions.

Philips Medical Systems Nederland B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20 Biplane Recall Affects 268 Units Worldwide (2025)

Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane imaging systems worldwide, including 102 in the United States. The recall cites deterioration of internal components that could disable motorized movements. Hospitals should stop using the devices immediately and follow the manufacturer’s recall instructions.

Philips Medical Systems
Systems may
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Health & Personal Care
HIGH
FDA DRUG

Zydus Lifesciences Chlorpromazine Hydrochloride 25 mg 100-count Tablets Recalled Nationwide (2025)

Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride tablets, 25 mg, 100-count bottles distributed nationwide by Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above the acceptable intake limit. Stop using the product and contact your healthcare provider or Zydus Pharmaceuticals (USA) Inc. for

Chlorpromazine Hydrochloride
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20 Recall Affects 2,114 Units Globally Over Power Component Deterioration

Philips Medical Systems Nederland B.V. recalls 2,114 Allura Xper FD20 imaging systems sold worldwide after reports that internal components may deteriorate. The recall covers models 722012, 722028 and 722006 with associated 510(k) numbers K102005 and K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949. If deterioration occurs, motorized movements may fail. Manual and imaging功能s,

Philips Medical Systems
Systems may
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Health & Personal Care
HIGH
FDA DRUG

Zydus Lifesciences Chlorpromazine Tablets Recalled for N-Nitroso Desmethyl Chlorpromazine Beyond FDA

Chlorpromazine Hydrochloride Tablets, 200 mg, 100-count bottle, manufactured by Zydus Lifesciences Ltd. and distributed by Northstar Rx LLC, are under recall nationwide in the United States. The CGMP deviation involves elevated levels of N-Nitroso Desmethyl Chlorpromazine. Consumers should stop use and contact their healthcare provider.

Zydus Lifesciences
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/20 Recall 115 Units Over Startup-Battery Risk (2025)

Philips Medical Systems Nederland recall 115 Allura Xper FD20/20 imaging systems worldwide after reports that the BIOS battery may deplete prematurely. The startup process may halt with no user alert. Hospitals and providers should stop using affected units and await manufacturer instructions.

Philips Medical Systems Nederland
The BIOS
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Tag Statistics

Total Recalls
262

Related Tags

electrical hazardelectronicimmediate actionreturn for refundcpsc regulatedfda regulatednhtsa regulatedstop use immediatelytoddler productinfant productadult productpet related