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. 2,367 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,367 in last 12 months

Showing 3034130360 of 48,219 recalls

DrugOctober 28, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol...

The Issue: Failed Stability Specifications: Low Out of Specification results for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Love My Tru Body

Recalled Item: Skinny Bee Diet capsules Recalled by Love My Tru Body Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: presence of undeclared sibutramine,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2016· Mondelez International

Recalled Item: Nabisco Oreo Fudge Creme Original Variety Recalled by Mondelez International...

The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 28, 2016· Aldi Inc

Recalled Item: Simply Nature Organic Red Split Lentils Recalled by Aldi Inc Due to...

The Issue: Product may contain undeclared wheat

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2016· Aldi Inc

Recalled Item: Simply Nature Organic Green Lentils Recalled by Aldi Inc Due to Undeclared Wheat

The Issue: Product may contain undeclared wheat

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2016· Mondelez International

Recalled Item: Nabisco Oreo Fudge Creme Mint Variety Recalled by Mondelez International Due...

The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 28, 2016· Life Rising Corp S

Recalled Item: Life Rising TT Side Head Regulator Recalled by Life Rising Corp S Due to...

The Issue: High levels of lead discovered in product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 28, 2016· Ion Beam Applications S.A.

Recalled Item: 12C (AdaPTinsight) Affected component: AdaPTinsight software Product Usage:...

The Issue: IBA is initiating this recall to address an issue identified with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 27, 2016· Amerisource Health Services

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets Recalled by Amerisource...

The Issue: Failed Dissolution Specifications: The firm was notified that there was a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: FLEXI NOZZLE SHORT Product Usage: These products are used for Recalled by...

The Issue: Product Defect; These products may produce a straight stream instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADett Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADgic Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: FLEXI NOZZLE LONG Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADomizer Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADdy Recalled by Teleflex Medical Due to Product Defect; These products...

The Issue: Product Defect; These products may produce a straight stream instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: Mucosal Atomization Device (MAD) Recalled by Teleflex Medical Due to Product...

The Issue: Product Defect; These products may produce a straight stream instead of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2016· 3M Company - Health Care Business

Recalled Item: 3M Universal Electrosurgical Pad Recalled by 3M Company - Health Care...

The Issue: 3M is recalling Universal Electrosurgical Pads because a report of an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing