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. 1,789 recalls have been distributed to Nevada in the last 12 months.
Showing 38181–38200 of 50,223 recalls
Recalled Item: Infinite 200 PRO in vitro diagnostic. Product Usage: The Tecan Recalled by...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite M1000 in vitro diagnostic. Product Usage: The Tecan Infinite...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite M1000 PRO in vitro diagnostic. Product Usage: The Tecan Recalled by...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2100IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 520. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2121IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CL 323i. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 730. Angiographic X-ray systems used in Recalled...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite F500 Recalled by Tecan US, Inc. Due to A firmware bug causes...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PowerLED / X-TEN / VOLISTA Surgical Light Systems are Recalled by Maquet...
The Issue: Maquet Suspension Arms used with PowerLED/X-TEN/Volista Surgical Light...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon PS X3 Tibial Insert Recalled by Stryker Howmedica Osteonics Corp....
The Issue: Stryker Orthopaedics received a report that 5537-G-319 No 3. Triathlon TS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nice! Powdered Sugar Mini Donuts 11.5 oz packaged in a Recalled by Walgreen...
The Issue: Nice! Powdered Sugar Mini Donuts may contain mold. Alleged illnesses have...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Enalapril maleate and hydrochlorothiazide tablets USP Recalled by Apotex...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Cleaver Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ring Transjugular Intrahepatic Access Set Product Usage: The Ring...
The Issue: Cook Inc. is initiating a voluntary recall of the Ring Transjugular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.