Health & Personal Care 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 Recalls Shoulder Prosthesis Over Labeling Error

Encore Medical, LP recalled 20 shoulder prosthesis implants on January 15, 2026. Incorrect labeling on the RSP Standard Humeral Socket Insert poses a high hazard risk. Affected products were distributed nationwide across multiple states.

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.

KOB GmbH Unna-Z Stretch Zinc Paste Bandage Recall for Labeling Error

Medline Unna-Z Stretch Zinc Paste Bandage faces a high-risk labeling error. The recall covers 35,328 units distributed in the U.S. and other regions. Manufacturers warn to stop use immediately and follow recall instructions.

RootStim Recalls Beard Growth Serum Due to Poisoning Risk

RootStim recalled Beard Growth Serum on January 15, 2026, due to inadequate child-resistant packaging. The product poses a serious poisoning risk to children. Consumers should stop using it immediately and secure it out of reach.

Ruahouine Hair Growth Serum Recalled Over Child Poisoning Risk

Ruahouine recalled its Hair Growth Serum on January 15, 2026, due to a poisoning hazard. The product lacks child-resistant packaging, violating safety standards. This poses a risk of serious injury or death if ingested by children.

Greenstone Recalls Methylprednisolone Tablets Due to Dosing Error

Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on the foil.

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.

KVK-Tech Inc. Recalls Oxycodone Hydrochloride Tablets Over Seal Defects

KVK-Tech Inc. recalled 31,676 packages of Oxycodone Hydrochloride Tablets on January 14, 2026. Defective seals may cause tablets to fall out, posing a health risk. Customers should stop using the product immediately and seek guidance from healthcare providers.

Edermy Recalls Medical Devices Due to Lack of 510K Clearance

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 7 Units Worldwide (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 Recalled 3 Endo-Model Replacement Plateau Implants (2026)

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