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. 1,075 recalls have been distributed to Utah in the last 12 months.
Showing 12761–12780 of 28,579 recalls
Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...
The Issue: Sterile packaging incomplete seals may compromise sterility of the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENTLEWAVE Recalled by Sonendo Inc Due to The console would continue to run...
The Issue: The console would continue to run for extended period when the foot pedal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Carbon Dioxide Reagent Kit Recalled by Abbott GmBH & Co. KG Due to...
The Issue: Abbott internal studies have determined that atmospheric Carbon Dioxide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to The firm...
The Issue: The firm received complaints that the EMPOWR Acetabular Impactor Balls were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Glide Aortic Cannula Recalled by Edwards Lifesciences, LLC Due to Their...
The Issue: Their is a possibility that the cannula may separate from its connector,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eagle 3000 Sterilizer Recalled by Steris Corporation Due to Potential for...
The Issue: Potential for the incorrect pressure safety valve being included in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer...
The Issue: The locking pin of the front wheel asse mbly of the Evolution Transfer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.