B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid-Position Issue (21,270 Units)
Potential for the lid of the catheter connector to be in the incorrect position.
1,216 recalls tagged with “replacement available”.
Potential for the lid of the catheter connector to be in the incorrect position.
Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower temperature than the true value, which may lead to a delay in managing fever-related symptoms or infection.
InSure ONE failed sensitivity testing when used with Test Card Lot T241102, which may result in false negative results.
Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
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.
Tablet/Capsules Imprinted with Wrong ID
Due to Users not having access to the Instructions for Use/User Manual due to it being password protected.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.