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. 1,712 recalls have been distributed to Nevada in the last 12 months.
Showing 46281–46300 of 50,223 recalls
Recalled Item: Betamethasone 6mg 10ml PF Recalled by Main Street Family Pharmacy, LLC Due...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Pellets 31mg Recalled by Main Street Family Pharmacy, LLC Due to...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Double Strength PGE1 40mcg 2ml Recalled by Main Street Family Pharmacy, LLC...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone LA 16mg/ml 30ml Recalled by Main Street Family Pharmacy, LLC...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lipotropic 50ml Recalled by Main Street Family Pharmacy, LLC Due to The firm...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Taper A prefilled syringes Recalled by Main Street Family Pharmacy, LLC Due...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lipotropic 50ml w/o methionine Recalled by Main Street Family Pharmacy, LLC...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Post-menopausal HCG Pk 2nd mont Recalled by Main Street Family Pharmacy, LLC...
The Issue: The firm received seven reports of adverse reactions in the form of skin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SYNCHRON System(s) Lactate (LACT) Reagent. Product Usage: Lactate (LACT)...
The Issue: Beckman Coulter has confirmed customer reports of LACT Lot M210077 failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure Nephrostomy Balloon Catheter. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...
The Issue: DJO, LLC has recently identified a product safety issue with the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for Recalled by...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 with Variable Spot Scanning Excimer System (STAR S4) Recalled by...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure nephrostomy Balloon Catheter Kit. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alair Bronchial Thermoplasty Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific has discovered an inconsistent "Use By" expiration date on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RigiflexTM 11 Single-Use Achalasia Balloon Dilator Recalled by Boston...
The Issue: Product labeled with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.