Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine Hydrochloride Injection, USP may contain 1% Lidocaine HCl Injection, USP and some vials labeled to contain 1% Lidocaine HCl Injection, USP may contain 0.5% Bupivacaine Hydrochloride Injection, USP
All Recalls
95,025 total recalls in our database
Vygon Dressing Change w/ Maxiswab - Product Usage: Custom Dressing Change kit, Product Code: AMS-8465CS.
Vygon U.S.A.
Compromised sterile barriers due to the Tyvek Lid not properly adhering to the Tray and has the the potential to cause an infection
Zimmer Natural Nail (ZNN) System-CMN Femoral Nail potential commingle between CCD angle 130 degree and 125 degree
Tranberg MR Stylet, 1.8mm/15G, 230mm, REF: 4013-06, Rx Only, Sterile EO - Product Usage: used with the TranbergΒΏ MR Introducer; a device used to aid the insertion of the Laser Applicator into the tissue.
CLINICAL LASERTHERMIA SYSTEMS AB
single use devices labeled as sterile may not have been adequately sterilized
Change Healthcare Enterprise Viewer - Product Usage: intended to be used with off-the-shelf hardware for the 2D and 3D display of DICOM and non-DICOM medical images, reports, and multimedia content.
CHANGE HEALTHCARE CANADA COMPANY
A software defect was identified where the Image Styles defined by presentation states from CHRS are not displayed in CHEV.
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized
Cannulated Screwdrivers may break at the driver tip along the shaft, near the handle extending surgery time and additional x-ray to identify the fragments from the breakages
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized
Three separate and unrelated problems attributed to the software used in the Evita V600, Evita V800, Babylog VN600 and Babylog VN800: 1. Restart of ventilation unit. 2. Incorrect FiO2 high and FiO2 low alarms. 3. SmartCare/PS (SC/PS) suspends weaning
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized
Products distributed as sterile may not have been adequately sterilized