These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
Olympus Corporation recalled 744 High Flow Insufflation Units on January 16, 2026. A software algorithm issue may lead to overpressure events during use. Patients and healthcare providers must stop using the device immediately.
Potential packaging failures, which could lead to a breach in the sterile barrier.
Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
Contains undeclared allergen (wheat) and colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed,
Specialty Process Labs recalled 58 grams of Thyroid, USP due to subpotency. The recall affects products distributed nationwide. Consumers should stop using the drug immediately and contact their healthcare provider.
Integra LifeSciences Corp. recalled 49,367 units of MediHoney Gel on January 16, 2026. The recall follows potential packaging failures that may compromise the sterile barrier. Affected products include model numbers 31805 and 31815, distributed worldwide.
Issue with software algorithm which may lead to overpressure events.
Issue with software algorithm which may lead to overpressure events.
Woodland Foods recalled 30,030 pounds of Arrowroot Flour on January 16, 2026. The product may contain foreign material that poses a health risk. Consumers should not consume the flour and should seek a refund or replacement.
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, 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, 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.
There is the potential for the length of the trocar shaft to be too long.
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 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 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.
Yixing Trading recalled KEAWIS crib mattresses on January 15, 2026. The mattresses pose a suffocation and entrapment hazard due to improper fit in cribs. Consumers should stop using the mattresses immediately and seek a refund.
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 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.