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. 1,077 recalls have been distributed to Nevada in the last 12 months.
Showing 12081–12100 of 50,223 recalls
Recalled Item: Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk...
The Issue: Undeclared allergen (peanuts) from incorrect master pack. Salad kit contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thistle Watermelon Berry Cold-Pressed Organic Juice watermelon strawberry...
The Issue: Manufactured using organic strawberries potentially contaminated with Hep A.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thistle Tropical Limeade Cold-Pressed Organic Juice watermelon pineapple...
The Issue: Manufactured using organic strawberries potentially contaminated with Hep A.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Software related alarm escalation defect occurs after approximately 25 days...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...
The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...
The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Avance CS2 Recalled by GE Healthcare, LLC Due to The base of...
The Issue: The base of the anesthesia system can have a crack and could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium...
The Issue: Due to Titanium plasma coating not present implant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLTIVE SuperPulsed Laser Fibers Recalled by Olympus Corporation of the...
The Issue: Device model and size for affected lots of Laser Fibers may be mismatched...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-SARS-CoV-2 IgG Quantitative Reagent Pack- Intended for use on VITROS¿...
The Issue: On-Analyzer Stability (OAS) time, supported for 6 weeks; not 8 weeks as is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Recalled by...
The Issue: Salmonella. Product made using recalled Jif peanut butter
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ortiga mas Ajo Rey con Omega 3 Recalled by Amazon.com, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mckesson GYNECATH H/S CATHETER 5FR (10/CS) Model Number: 11-19610 Recalled...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Comply INDICATOR Recalled by Mckesson Medical-Surgical Inc. Corporate...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. STERIS CORP Celerity Celerity 20 Sterilization Indicator Challenge Pack...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical PREFILTER Recalled by Mckesson Medical-Surgical Inc....
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Skin Adhesive McKesson LiquiBand Exceed 0.4 mL Liquid Dome Recalled by...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. SPS MEDICAL SUPPLY Steam Indicator Strip SPSmedical Sterilization...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.