electrical hazard Recalls

Mentor CPX 4 Breast Tissue Expanders Recalled in 2026 for Dull Needle Tip Hazard

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

XTANT Medical Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm Recalled for Mislabeling of Screw S

Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.

Molded Products MPC-130 See Luer Cap Set Recalled for High-Risk Assembly Issue (2026)

Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.

Abiomed Impella Automated Controller Recall 62 Units in 2026

Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5 (0550-0008*) pumps.

Medline Recalls 14,379 Olympus Biopsy-Valve Kits in 2026

Medline Airway Exam Kit Recalled for 14,379 Units Over Olympus Valve Detachment (2026)

Medtronic MiniMed 530G Insulin Pumps Recalled for Delivery Errors in 2026 (13,429 Units)

Medline ENFIT G-Tube Connector ENFIT1010GC Recalled for Leakage Risk (651,789 Units, 2026)

Medtronic MiniMed 720G Insulin Pump Recall 2026 Affects 37,458 Units Worldwide

Medtronic MiniMed 620G Insulin Pump Recall Impacts 799 Units Worldwide (2026)

Medtronic MiniMed Paradigm Real-Time Insulin Pump Recalled for 29,074 Units Worldwide (2026)

Medtronic MiniMed Paradigm Insulin Pumps Recalled 73,656 Units Worldwide in 2026

Olympus OER-Pro Endoscope Reprocessor Recall for 3,354 Units Over MAJ-1443/1444 Compatibility (2026)

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Olympus MAJ-1443/MAJ-1444 Endoscope Suction Valves Recalled in 2026

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Eptifibatide Injection Recalled Over Labeling Error

Slate Run Pharmaceuticals recalled Eptifibatide Injection on February 12, 2026. The recall affects all lots of the 75 mg/100 mL vial due to incorrect dosing information. Healthcare providers and consumers must stop using the product immediately.

Waldemar Link Embrace Drill Tower Recall 74 Units in 2026

The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.

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

Products contain undeclared milk and soy.

Reflexion Medical Recalls 12 RefleXion X1 Radiotherapy Systems for Software Defect (2026)

12 Million TRUE METRIX Blood Glucose Meters Recalled Due to E-5 Error Code Risk

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

Augmentation devices failed bacterial endotoxin testing.