battery powered Recalls

293 recalls tagged with “battery powered”.

Food & Beverages
HIGH
FDA FOOD

Juniper Granola Junebar Recall 2026: 1,800 Snack Bars Recalled for Undeclared Milk and Soy

Juniper Granola recalled 1,800 Junebar Chocolate Cherry All Natural Snack Bars sold in New York after undeclared milk and soy were found. The bars carry Lot L1300 and variants L1300A and L1300B. They were produced in a facility that also processes gluten, peanuts, and sesame. Consumers should not eat these bars and should contact Juniper Granola for refunds or replacements.

Juniper Granola
Products contain
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Thyroid Shield Recall 2026 Affects 41,962 Units Worldwide

Burlington Medical recalled 41,962 Thyroid Shield units worldwide after identifying attenuation degradation that could shorten the device’s lifespan. The attenuation material may degrade over time, reducing shielding effectiveness. Patients and healthcare providers should stop using the device immediately and follow the recall instructions in the manufacturer notice.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

International Life Sciences Recalls Artelon FlexBand Plus Augmentation Devices for Endotoxin Testing

International Life Sciences recalled Artelon FlexBand Plus augmentation devices after endotoxin testing failures. The recall affects devices with REF 41054 and REF 41057 distributed worldwide. Patients and healthcare providers must stop using the devices immediately and follow manufacturer instructions for recall return.

International Life Sciences
Augmentation devices
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Health & Personal Care
HIGH
FDA DEVICE

Trividia Health TRUE METRIX GO Recall for E-5 Error Misleading Labeling (1.4M, 2026)

Trividia Health's TRUE METRIX GO blood glucose kits sold at Walgreens, CVS and other retailers are recalled worldwide. The labeling fails to clearly emphasize that an E-5 error could indicate very high blood glucose and require immediate action. Consumers should stop using the device and follow manufacturer guidance.

Trividia Health
The system
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Health & Personal Care
HIGH
FDA DEVICE

International Life Sciences Recalls Artelon FLEXBAND TWIST Augmentation Devices for Endotoxin Test F

International Life Sciences issued an active recall of Artelon FLEXBAND TWIST augmentation devices. The devices were distributed worldwide, including nationwide in the United States. The recall concerns failures in bacterial endotoxin testing that could pose a infection risk; users should stop using the device and follow recall instructions from the manufacturer.

International Life Sciences
Augmentation devices
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Recalled Kitosun Submersible LED Lights
HIGH
CPSC

Kitosun Submersible LED Lights Recalled Over Battery Ingestion Risk

Kitosun recalled Submersible LED Lights on February 5, 2026, due to a serious ingestion hazard. The lights contain accessible lithium batteries that pose a risk of internal chemical burns or death if ingested by children. Consumers should stop using the product immediately and return it for a full refund.

Kitosun Submersible LED Lights
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Recalled 125 Imactis CT-Navigation System Stereotaxic Accessories in 2026

GE Medical Systems recalled 125 Imactis CT-Navigation System stereotaxic accessories distributed worldwide to healthcare facilities. The recall cites a potential mismatch between the simulated needle trajectory and the actual trajectory. Healthcare providers should stop using the devices immediately and follow the manufacturer's recall instructions.

GE Medical Systems
There is
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Health & Personal Care
HIGH
FDA DEVICE

Tandem Diabetes Care Insulin Infusion Pumps Recalled 1,380 Units in 2026 Over Czech Guide Error

Tandem Diabetes Care recalled 1,380 insulin infusion pumps distributed internationally in the Czech Republic and Slovakia after translation errors in the Czech user guide could cause unintended insulin delivery. The most significant error told users to verify the infusion set is connected to the body when it should be confirming it is not connected. Following this instruction could result in a hyp

Tandem Diabetes Care
The Czech
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 780G Recall 2026: 26,851 Pumps Hit Over Software Defects

Medtronic MiniMed recalled 26,851 MiniMed 780G insulin pumps sold worldwide, including the United States and Israel. Three software defects tied to updates 6.60, 6.61, and 6.62 could misdose insulin. Stop using the affected pumps and follow the recall letter for instructions.

Medtronic MiniMed
Three software
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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella RP Recall 179 Units for Sensor Drift Risk (2026)

Abiomed recalled 179 Impella RP devices worldwide after a differential pressure sensor may drift. The fault can cause sensor values to drift, potentially affecting patient care. Stop using the device immediately and follow the recall instructions, including contacting Abiomed or your healthcare provider.

Abiomed
Differential pressure
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Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Screw System Recalled for MRI Heating Risk in 5,568 Units (2026)

I.T.S. GmbH has recalled 5,568 units of the I.T.S. Screw System sold nationwide in the United States after MRI safety tests showed higher RF-induced temperature increases under some MRI conditions than the IFU outlined. The defect involves MRI RF heating that could burn patients. Patients and healthcare providers should stop using the device immediately and follow the recall instructions.

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

Datascope CS300 IABP Recall 2026 Aims to Update IFU Battery Specs (10897 Units Worldwide)

Datascope Corp. recalls 10,897 CS300 IABP devices sold through healthcare providers worldwide after determining the battery runtime and cycle specifications in the Instructions for Use must be updated. The issue is an information update rather than a device fault. Stop using the device immediately and follow the manufacturer’s recall instructions. Contact Datascope Corp. or your healthcare team to

Datascope
The firm
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Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Pelvic Reconstruction System Recall for MRI Heating Risk (46,637 Units) 2026

I.T.S. recalled 46,637 pelvic reconstruction system components nationwide in the United States after MRI safety testing showed higher RF-induced heating than the IFU stated. The issue centers on MRI heating under certain conditions that could injure patients. Patients should stop using the devices and follow manufacturer recall instructions.

I.T.S. GmbH
Updated MRI
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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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Tag Statistics

Total Recalls
293

Related Tags

infant productadult productstop use immediatelyreturn for refundglassplasticimmediate actionchoking hazardlaceration riskburn riskelectrical hazardpoisoning risk