Product Recalls in Utah
Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,563 recalls have been distributed to Utah in the last 12 months.
Showing 15321–15340 of 28,579 recalls
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...
The Issue: There is a potential security vulnerability related to the use of the remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minimed Model 500 Remote Control (MMT-500 Recalled by Medtronic Inc. Due to...
The Issue: There is a potential security vulnerability related to the use of the remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Multix MT (model number 8395415 or 8395399 or 8395381) Recalled by...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio MAX (model number 10762470) with Tube stand 3D V Recalled by Siemens...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio (model number 10281013 or 10281163) with Tube stand 3D Recalled by...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparoscopy Instruments Instructions For Use (IFU) for the following:...
The Issue: The Manual cleaning process and the usability of the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multix Fusion system is a radiographic system: Models: Multix Fusion...
The Issue: Steel cables inside the lifting column of the overhead tube, may rapture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palcam Agar Base Recalled by Acumedia Manufacturers, Inc. Due to Expiration...
The Issue: Expiration date on the label is incorrect. Correct expiration date was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System With MedNet/ Smart Card Plug And Play Module...
The Issue: A software malfunction of the infuser when used with a MedNet Custom Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosll ReadiPlasTin (10 mL Size) Recalled by Instrumentation Laboratory Co....
The Issue: There is a potential for increased imprecision, out of range quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sterEOS workstation Recalled by EOS Imaging Due to 3D projections may be...
The Issue: 3D projections may be incorrect when the pair of images used is a secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Gauze Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.