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. 955 recalls have been distributed to Nevada in the last 12 months.
Showing 41461–41480 of 50,223 recalls
Recalled Item: Prescription eyeglass safety lenses. Vision correction Recalled by Eyemart...
The Issue: Prescription eyeglass safety lenses did not meet specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...
The Issue: Correction due to the detection of a motor sensor failure in the Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...
The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roma Tomatoes Recalled by Expo Fresh L.L.C Due to Potential Salmonella...
The Issue: Expo Fresh is recalling Roma Tomatoes because they have a potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MethylPREDNISolone TABLETS Recalled by Qualitest Pharmaceuticals Due to...
The Issue: Subpotent; 6 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN SODIUM Recalled by Hospira Inc. Due to Presence of Particulate...
The Issue: Presence of Particulate Matter: A particulate, confirmed as human hair, was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine Hydrochloride Injection Recalled by Hospira Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specification: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...
The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cushing perforating drills are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI¿ Pediatric Anesthesia Breathing Circuits Recalled by Teleflex...
The Issue: The pediatric breathing circuits can crack prior to and during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: An external vein stripper is an extravascular device used to Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: An endometrial suction curette is a device used to remove Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gardner-Wells wrenches are used in traction skull tongs for traction...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cloward Spanner gauges are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Ortho Clinical Diagnostics (OCD) identified an anomaly with Software Version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Schoitz weights are manual devices used with Schoitz tonometers and Recalled...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A uterine tenaculum is a hook-like instrument used to seize Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics (OCD) identified an anomaly with Software Version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson cranial drill sets (w/ brace and 5 attachments) are Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Traction tong replacement screws Recalled by Instrumed International, Inc....
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.