stop use immediately Recalls

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.

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.

Morgan Lane Recalls Children's Pajama Sets Over Burn Hazard

Morgan Lane recalled Asher Pajama Sets on January 15, 2026, due to a burn hazard. The pajamas do not meet mandatory flammability standards for children's sleepwear. Consumers should stop using the pajamas immediately and request a refund.

R.X.Y Bicycle Helmets Recalled for Serious Head Injury Risk

R.X.Y recalled adult bicycle helmets on January 15, 2026, due to safety violations. The helmets fail to meet mandatory impact standards, posing a serious risk of injury or death. Consumers should immediately stop using the helmets and seek a refund.

Curtis International Recalls Frigidaire Minifridges Over Fire Risk

Greatale Recalls Self-Feeding Pillows Due to Suffocation Risk

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.

Aonic Complete Hers Dietary Supplement Recalled for Contamination Risk

Aonic Inc. recalled 3,630 bottles of Aonic Complete Hers dietary supplement on January 15, 2026. Possible contamination with coliforms, E. coli, and Pseudomonas aeruginosa prompted the recall. Consumers in Utah should stop using the product immediately.

LUBNA QUALITY PRODUCTS Recalls Mung Beans Over Pesticide Hazard

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.

Rose and Shore Recalls 5,067.1 Cases of 14" Margarita Thin Crust Pizza for Metal Fragments (2026)

potential foreign object (metal pieces) in ingredient (Tomatoes)

Sevillo Fine Foods Recalls 520 Units of Slow Roasted Diced Tomatoes Over Metal Fragments (2026)

Product may contain foreign material (metal fragments).

Sevillo Fine Foods Recalls 2,372 Units of Slow Roasted Diced Tomatoes (2026 Recall)

Product may contain foreign material (metal fragments).

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

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.