Product Recalls in Nevada
Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,065 recalls have been distributed to Nevada in the last 12 months.
Showing 14521–14540 of 28,334 recalls
Recalled Item: Wire Guide Recalled by Cook Inc. Due to The wire guide may be incorrectly...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kwart Retro-Inject Ureteral Stent Set Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sof-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Entry Set Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urethral Dilation Balloon Catheter with Open Tip Recalled by Cook Inc. Due...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bander Ureteral Diversion Open-End Stent Set Recalled by Cook Inc. Due to...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angled Tip Ureteral Catheter Set with Bentson PTFE Wire Guide Recalled by...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universa Firm Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical...
The Issue: Complaints of the snare loop not completely retracting and/or misshaping of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT MAGNESIUM Recalled by Abbott Laboratories, Inc Due to Abbott...
The Issue: Abbott internal testing has identified that the Magnesium urine application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M220 F12 surgical microscope The Leica M220 F12 surgical Recalled by...
The Issue: The M220 optics may unintentionally drop into the surgical field, risking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity All Purpose Sponges Recalled by Cardinal Health 200, LLC Due to...
The Issue: Curity All Purpose Sponges were not sterilized and distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLAS Loading Car Recalled by Steris Corporation Due to The ATLAS loading...
The Issue: The ATLAS loading car may not remain fully engaged with the latch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vergene Amplification Tray - 700uL Recalled by Luminex Corporation Due to On...
The Issue: On lot of VERIGENE(R) BC-GP Utility Kits (20-011-018) were labeled with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse(TM) Treatment Planning System with Proton Convolution Superposition...
The Issue: There is an anomaly with the Eclipse(TM) Treatment Planning System [TPS]...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 7.0T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T X-series Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.