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 15701–15720 of 50,223 recalls
Recalled Item: Xtra Butter Microwave Popcorn bags packaged in cardboard boxes labeled...
The Issue: Buttered microwave popcorn bags were packaged inside a regular popcorn box...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lipodrene With 25mg Ephedra Extract 100CT Recalled by Hi Tech...
The Issue: The firm was notified by the FDA that the product contains the unapproved...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Imperia Elita Vitaccino Coffee Recalled by DASH XCLUSIVE Due to Marketed...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis determined presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DiBAR LABS Hand Sanitizer (ethyl alcohol 70%) Recalled by DIBAR NUTRICIONAL...
The Issue: Chemical Contamination: FDA analysis found 3 lots of DiBAR hand Sanitizer to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVANCE HAND SANITIZER Recalled by DIBAR NUTRICIONAL S DE RL DE CV Due to...
The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ProtectoRx (ethyl alcohol 70%) Recalled by DIBAR NUTRICIONAL S DE RL DE CV...
The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DiBAR LABS Hand Sanitizer Recalled by DIBAR NUTRICIONAL S DE RL DE CV Due to...
The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT....
The Issue: The HAT trial contains a retaining ring that has shown the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skyton Bracket Flatscreen Recalled by Skytron, Div. The KMW Group, Inc Due...
The Issue: Failure of the FS32 Monitor Brackets from the mounting block could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: novaplus Recalled by Medical Action Industries, Inc. 306 Due to There is a...
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to Elevated...
The Issue: Elevated rates of false negative results may occur when using blood culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog...
The Issue: Due to a component failure, ventilators may unexpectedly shut down or have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of...
The Issue: Standard packed within NEFA kit has been assigned incorrectly. Calibrating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit...
The Issue: A risk exists during impacting of the acetabular cup into the bone the plugs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascadia AN Interbody Convex 10x22x14mm Catalog Number: 6101-2102214NC-G2...
The Issue: Mislabeled product labeling incorrect length or height, or length and height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare Plus Blood Lead Test Kit Catalog Number 82-0004 Recalled by...
The Issue: Magellan has received reports that control tests of either the Low-Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.