B Braun Medical SESK Pain Management Tray Recall Affects 2,450 Units Nationwide (2025)
Potential for the lid of the catheter connector to be in the incorrect position.
225 recalls tagged with “pet related”.
Potential for the lid of the catheter connector to be in the incorrect position.
No ingredient label. Product contains undeclared allergens (peanuts, sesame, wheat, and soy)
Potential for the lid of the catheter connector to be in the incorrect position.
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
It was found that the shaft for mounting the X-ray tube unit on the support may break. In addition, it was found that the protective parts might not work effectively only when the shaft was broken while being operated toward the front while lifting.
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Torrey Pines Dermatology & Laser Center's Benzaderm BPO Cleanser recall remains active. The FDA-listed recall covers benzoyl peroxide cleanser lot numbers 58170A and 58172A with expiration 09/2025. Consumers should stop use and contact the recall coordinator.
Private Label Skin Care Inc. recalled edunn clarity BP Treatment Cleanser 10% after benzene was detected. The recall covers lot numbers 58170A and 58172A with expiration September 2025. The product was distributed in California and Georgia.
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Possible presence of stones in product
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.
Possible presence of stones in product

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas recalls its BF-P150 bronchoscope after updates to the instruction for use. The recall covers 1,019 units outside the U.S. Distribution was nationwide in the U.S. The agency classifies this as a high-hazard issue.
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Undeclared Sesame, Undeclared Yellow 5, Red 40, Yellow 6