Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,540 recalls have been distributed to Wyoming in the last 12 months.
Showing 6561–6580 of 48,219 recalls
Recalled Item: Febuxostat Tablets 40mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zolpidem Tartrate Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...
The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adrenalin (epinephrine) Injection 1mg/mL Recalled by Henry Schein Inc. and...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fosfomycin Tromethamine Granules for Oral Solution Recalled by Ascend...
The Issue: Failed Impurities/Degradation Specification: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrogen Peroxide Oral Rinse Recalled by Den-Mat Holdings, LLC Due to CGMP...
The Issue: CGMP Deviations: products may not conform to the labeled specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OralProCare medicated lip treatment Recalled by Den-Mat Holdings, LLC Due to...
The Issue: CGMP Deviations: products may not conform to the labeled specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC*...
The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC* Gastric-Jejunal Feeding Tube Recalled by Avanos Medical, Inc. Due to...
The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: W&H Surgical handpiece S-12. For Surgical treatment of dental hard Recalled...
The Issue: 1:2 speed increasing surgical handpieces have been incorrectly laser marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The Emergency...
The Issue: The Emergency Priming Line, a component of the HLS Set, may have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The...
The Issue: The Emergency Priming Line, a component of the HLS Set, may have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Water Filter MAJ-2318. This MAJ-2318 water filter has been designed Recalled...
The Issue: Water filter may have been assembled incorrectly, resulting in unfiltered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenoxybenzamine Hydrochloride Capsules Recalled by Amneal Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IV Start Kit Recalled by Medical Action Industries, Inc. 306 Due to The kits...
The Issue: The kits contain saline flush syringes which were recalled by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.