T.C.A 30% Acid Sol, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
Western Drug
💊 Drugs Class I - Dangerous
Lack of Assurance of Sterility
All Recalls
95,102 total recalls in our database
Monitor Ceiling Suspension system may fall
Monitor Ceiling Suspension system may fall
Monitor Ceiling Suspension system may fall
🏥 Medical Devices Class I - Dangerous
The expiration date encoded in the UDI barcode on the label on the product carton and the peelable patient identification label is incorrect.
Monitor Ceiling Suspension system may fall
🏥 Medical Devices Class I - Dangerous
The firm had received a complaint alleging that a medical professional had difficulty inserting a guide wire into a needle
Monitor Ceiling Suspension system may fall
🏥 Medical Devices Class I - Dangerous
IOL Master software versions 7.5 and 7.7 calculation printouts and exported reports can contain the wrong IOL power data.
Copper NiTi Preformed Archwires; Copper NiTi 40 BAF .016X.022 LO Pk10, Part No. 211-0952. Intended to provide tooth movement.
Ormco/Sybronendo
🏥 Medical Devices Class I - Dangerous
Ormco Corporation is recalling Copper NiTi Preformed Archwires because the product transformation temperature as listed on the labeling is incorrect.
Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost ; Model: 704060/706037
Philips Medical Systems
🏥 Medical Devices Class I - Dangerous
The hook does not securely hold the footplate in vertical position. Therefore the footplate can fall or swing down and may hurt the operator or patient.
🏥 Medical Devices Class I - Dangerous
Medtronic has confirmed an issue with InSync III CRT-pacemaker devices related to long-term battery performance. The root cause is unexpected high battery impedance.
Patient Support Material Number: 9890 010 87431, used with:EasyDiagnost ; Model: 706050
Philips Medical Systems
🏥 Medical Devices Class I - Dangerous
The hook does not securely hold the footplate in vertical position. Therefore the footplate can fall or swing down and may hurt the operator or patient.
🏥 Medical Devices Class I - Dangerous
Microcatheter may have circumferential defects (cracks) along its shaft.
These custom sterile surgical kits contain the component, ECOLAB ORS Fluid Warming and Slush Drape, which was recalled due to the possibility that the sterile packaging may contain small channels in the seal of the pouch.
🏥 Medical Devices Class I - Dangerous
The products have been found to intermittently exhibit a seal failure during use.
HYDRO-TEMP(R) Neonatal Temperature Skin Sensor, REF HNICU-32, 50 units per box, NON STERILE, Rx only.
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal manufactured four lots of HNICU-32, Hydro-Temp(R) Neonatal Temperature Skin Sensor incorrectly. The pins contained in the probe were soldered incorrectly. When probe is connected to the proper port, this defect results in the inability to read or display temperatures on the infant warming system.
Monitor Ceiling Suspension system may fall
🏥 Medical Devices Class I - Dangerous
Stryker Orthopaedics has received two customer complaints regarding Duracon Tibial Wedge implants puncturing the packaging's Tyvek lid(s).
Radiesse (+) Lidocaine Injectable Implant 1.5cc, P/N: 8063M0K1. Indicated for subdermal implantation for the correction of moderate to severe facial wrinkles and folds.
Merz North America
🏥 Medical Devices Class I - Dangerous
The expiration date encoded in the UDI barcode on the label on the product carton and the peelable patient identification label is incorrect.