lithium battery Recalls

262 recalls tagged with “lithium battery”.

Food & Beverages
HIGH
FDA FOOD

Mangalm Mangalm Tops GOLD Lime Pickle Recalled for Erucic Acid Adulteration (2026)

Mangalm LLC recalls 40 cases of Tops GOLD Lime Pickle, 31.74 oz jars, produced in India and distributed to California, Nevada, Oregon, Utah and Washington. The recall follows potential adulteration with erucic acid from mustard oil. Consumers who have purchased the product should not consume it and should contact Mangalm LLC for a refund or replacement via email.

Mangalm
Potential adulteration
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Food & Beverages
LOW
FDA FOOD

Mangalm Tops GOLD Stuffed Red Chilli Pickle Recall for Possible Erucic Acid Adulteration (2026)

Mangalm LLC recalled 40 cases of Tops GOLD Stuffed Red Chilli Pickle, 31.74 oz cans, distributed in California, Nevada, Oregon, Utah and Washington. The recall is due to potential adulteration with erucic acid from mustard oil. Consumers should not consume this product and should contact Mangalm LLC by email for a refund or replacement.

Mangalm
Potential adulteration
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Health & Personal Care
HIGH
FDA DEVICE

I.T.S. GmbH LRS Orthopedic System Recall: 176 Units for MRI Heating Risk (2026)

ITS GmbH recalled 176 units nationwide in the United States after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions. The issue could cause burns during MRI exposure. Healthcare providers and patients should stop using the device immediately and follow recall instructions.

I.T.S. GmbH
Updated MRI
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory GEM Premier 5000 PAK Recall 2026 for 51 Units

Instrumentation Laboratory recalled 51 GEM Premier 5000 PAK cartridges worldwide after complaints of PCSND errors during warm-up. These errors can cause GEM PAK cartridges to eject. The recall could delay results and affect patient management. Stop using the affected cartridges and follow recall instructions from Instrumentation Laboratory.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalls GEM Premier 5000 GEM PAK Cartridges Over PCSND Errors, 1,989 US/3

GEM Premier 5000 recall announced for 1,989 units distributed worldwide, including the US and numerous other countries. The issue involves GEM PAK cartridges experiencing Process Control Solution Not Detected errors during warm-up, causing ejections and potential delays in patient results. Stop using the device and follow manufacturer recall instructions.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalled 180 GEM Premier 5000 PAK Cartridges for PCSND Errors (2026)

Instrumentation Laboratory recalls 180 GEM Premier 5000 PAK cartridges distributed worldwide after reports of PCSND errors during warm-up. During warm-up, GEM PAKs may eject and require insertion of a new GEM PAK. Hospitals should stop using the affected cartridges and follow the manufacturer's recall instructions.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory GEM Premier 5000 PAK Recalled for PCSND Warm-Up Errors (30 Units, 2026)

Instrumentation Laboratory is recalling 30 GEM Premier 5000 PAK cartridges distributed worldwide, including the United States. The affected cartridges may experience PCSND errors during warm-up, causing GEM PAKs to eject. Stop using the product and follow recall instructions from the manufacturer for refunds or replacements.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Implant Recall: Endo-Model Replacement Plateau 15-8521/09 Looks to Detach from Screw (

Waldemar Link GmbH & Co. KG recalls 8 units of Endo-Model Replacement Plateau worldwide after a reported risk that a bushing could detach from the screw shaft due to a longitudinal fracture. The recall also covers US distribution in New Jersey. Health authorities have classified the risk as high. Patients and healthcare providers should stop using the device immediately and follow recall guidance.

Waldemar Link GmbH & Co. KG
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Olympus ShockPulse-SE Lithotripsy System Recall Expands to 55 Units in 5 Countries (2026)

Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.

Olympus
Mis-wired component-the
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Liquid DayQuil 12/8oz for CGMP Issues (2025)

Gold Star Distribution is recalling Liquid DayQuil 12/8oz distributed nationwide in the United States. The recall cites CGMP deviations and insanitary conditions, including rodent exposure at the distribution center. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution for guidance.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Carmex Lip Balm Recalled by Gold Star Distribution for 12-Count Jars and Tubes (2026)

Gold Star Distribution Inc. is recalling Carmex lip balm in 12-count jars and 12-count tubes distributed nationwide in the United States. The recall cites CGMP deviations and insanitary conditions at the distribution center, including rodent exposure. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution for guidance.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Vehicles & Parts
HIGH
NHTSA

Hyundai IONIQ 6 Recall Expands for Charging Port Door Detachment

Hyundai Motor America recalls 2023-2025 IONIQ 6 electric vehicles due to a charging port door panel that may detach. Dealers will apply adhesive as the remedy. Owner letters begin November 10, 2025. VINs searchable on NHTSA as of September 13, 2025.

Hyundai
A detached
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Recalled INIU Power Bank – model BI-B41
HIGH
CPSC

INIU Recalls 10,000mAh BI-B41 Power Banks Over Fire Hazard (2025 Recall)

INIU recalled 10,000mAh portable power banks sold on Amazon after identifying a fire risk from overheating. The recall covers BI-B41 models with serial numbers 000G21, 000H21, 000I21 and 000L21. Consumers should stop using the recalled power banks immediately and contact INIU for a full refund.

INIU
The lithium-ion
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Recalled KTEBO Writing Tablet Toys in Blue/Pink (front)
HIGH
CPSC

KTEBO Writing Tablet Toys Recalled Over Battery Ingestion Risk on Amazon (2025)

KTEBO recalled its Writing Tablet Toys sold on Amazon on December 4, 2025. The screw securing the battery compartment containing a button cell battery does not remain attached as required. This creates a risk of ingestion with potential serious injury or death. Consumers should stop using the 2-pack sets immediately and contact KTEBO for a free replacement.

KTEBO
The recalled
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Recalled Spartan Riding Lawn Mower (SRT-XD)
MEDIUM
CPSC

Spartan Mowers Recalls 2025 SRT-XD and KGZ-XD Riding Mowers for Steering Damper Hazard

Spartan Mowers recalled certain Model Year 2025 SRT-XD and KGZ-XD zero-radius-turn riding mowers sold through Spartan dealers nationwide. A steering arm damper can be installed incorrectly, creating a bouncing motion and loss of operator control. Owners should stop using the recalled mowers and contact an authorized Spartan dealer for a free inspection and repair.

Spartan Mowers and UTVs
The riding
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Food & Beverages
HIGH
FDA FOOD

Face Rock Creamery Vampire Slayer Garlic Cheddar 6 oz Recalled for Listeria Risk (2025)

Face Rock Creamery recalled 16 units of Vampire Slayer Garlic Cheddar Cheese, 6 oz, distributed in Oregon after an FDA environmental sample detected Listeria monocytogenes in the packaging area. The hazard is a contamination risk that could cause life-threatening infection in some populations. Consumers should not eat the cheese and should contact Face Rock Creamery for a refund or replacement.

Face Rock Creamery
FDA environmental
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