battery powered Recalls

Burlington Medical Recalls 961 Caps for Medical Devices Over Attenuation Degradation (2026)

Potential for attenuation degradation over time, decreasing the lifespan.

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

Potential for attenuation degradation over time, decreasing the lifespan.

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

Augmentation devices failed bacterial endotoxin testing.

International Life Sciences Recalls Artelon FlexBand Dynamic Matrix 31057 for Endotoxin Testing Fail

Augmentation devices failed bacterial endotoxin testing.

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

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

Augmentation devices failed bacterial endotoxin testing.

Kitosun Submersible LED Lights Recalled Over Battery Ingestion Risk

Dresbe LED Christmas Headbands Recalled Over Battery Ingestion Risk (2026)

Dresbe LED Christmas Headbands are recalled in 2026 after a battery ingestion hazard was identified. The recall covers a two-pack set labeled HB-052. Stop using the headbands and contact Dresbe for a full refund.

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

There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.

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

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

Beckman Coulter Mishima K.K. DxC 700 AU Recall for 142 Units Over Calibration Delay Risk (2026)

Olympus MAJ-1218 Single Use Biopsy Valve Recall Expanded in 2026 for Rubber Fragment Detachment

Potential for rubber fragment detachment during use.

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

Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.

Datascope CS100 IABP Recall 2026: 10,897 Devices for Battery Runtime Update

The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.

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

Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

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

Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

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

Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

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

The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.

Instrumentation Laboratory GEM Premier 5000 PAK Recall 2026 for 51 Units