electrical hazard Recalls

Olympus Insufflation Unit Recalled Over Software Malfunction

Issue with software algorithm which may lead to overpressure events.

Olympus Insufflation Unit Recalled Due to Software Hazard

Issue with software algorithm which may lead to overpressure events.

CVS Wound Care Device Recalled Due to Sterile Barrier Breach

CVS recalled 2,906 units of its wound care device on January 16, 2026. The recall stems from potential packaging failures that may compromise sterility. Affected products include model number CVS405406, distributed across multiple states and internationally.

Encore Medical Recalled Humeral Socket Insert Over Labeling Issues

Encore Medical, LP recalled 20 units of its RSP Humeral Socket Insert on January 15, 2026. The recall stems from incorrect labeling on knee and humeral socket implants. Patients and healthcare providers should stop using the device immediately.

Aesculap MINOP TROCAR 150MM Recall for 126 Units in 2026

There is the potential for the length of the trocar shaft to be too long.

HEZI Power Strips Recalled Over Electrocution Risk

HEZI recalled power strips on January 15, 2026, due to an electrocution hazard. The power strips have an ungrounded metal enclosure that can become energized. Consumers should stop using them immediately and seek a refund.

Encore Medical Recalls EMPOWR 3D Knee Implants Due to Labeling Issues

Encore Medical, LP recalled 14 EMPOWR 3D Knee implants on January 15, 2026. The implants contain incorrect labeling that poses a risk to patients. Healthcare providers should stop using the device immediately and follow recall instructions.

Edermy Recalls PIE Trolley System Due to Lack of 510K Clearance

Laerdal Medical Recalls Suction Units Over Electromagnetic Noise Hazard

Laerdal Medical recalled 1,202 Compact Suction Units on January 13, 2026. The recall affects models LCSU 4, 800 ml and LCSU 4, 300 ml due to excessive electromagnetic noise. Patients and healthcare providers must stop using the devices immediately.

Baxter Infusion Pump Recalled Due to Incomplete Testing

Baxter Healthcare recalled five infusion pumps on January 13, 2026. The pumps were released without full testing, including critical occlusion alarm checks. Healthcare providers and patients must stop using the device immediately.

Medtronic Recalls Octopus Nuvo Tissue Stabilizer Due to Assembly Issue

During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

Waldemar Link Endo-Model Replacement Plateau Recall for Detachment Risk (2026)

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Waldemar Link Endo-Model Replacement Plateau Recalled for Detachment Risk

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Teva Isotretinoin 30 mg Recall Active for Potency Variations in 10-Count Packs

Teva Pharmaceuticals USA, Inc. recalls 21,984 packages of Isotretinoin Capsules, USP, 30 mg. The lots are distributed to Florida, Ohio, Puerto Rico and Mississippi. The recall is active as of April 15, 2026.

Waldemar Link Endo-Model 15-0027/12 Implant Recall 2026 for Detachment Risk

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Waldemar Link Medical Devices Recall 4-Endo-Model Replacements for Plateau Screw Bushing Detachment

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

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

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Ford 2025 Explorer and Lincoln Aviator Recalled for Rear-View Camera Software Issue (2026)

FUJIFILM Healthcare Recalls X-ray Generator Over Fire Hazard

Maquet Cardiopulmonary Recalls Venous Bubble Sensor Due to Cable Risk

Maquet Cardiopulmonary Gmbh recalled 3,050 Venous Bubble Sensors on January 9, 2026. Internal investigations revealed issues with the durability of the connecting cable. Excessive bending can lead to device failure, posing a risk to patient safety.