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. 2,557 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,557 in last 12 months

Showing 38013820 of 13,375 recalls

DrugAugust 20, 2021· Washington Homeopathic Products, Inc.

Recalled Item: ZTE 1015 Formula Recalled by Washington Homeopathic Products, Inc. Due to...

The Issue: Out-of-specification test results obtained for identification testing based...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2021· Eli Lilly & Company

Recalled Item: Trulicity (dulaglutide) Recalled by Eli Lilly & Company Due to Labeling:...

The Issue: Labeling: Label error on declared strength - autoinjector devices labeled as...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2021· Rhodes Pharmaceuticals, L.P.

Recalled Item: Oxycodone Hydrochloride Tablets Recalled by Rhodes Pharmaceuticals, L.P. Due...

The Issue: Presence of Foreign Tablets/Capsules; A single foreign tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2021· Prescription Labs Inc dba Greenpark

Recalled Item: Spironolactone Ophthalmic Solution 0.005 mg/mL Recalled by Prescription Labs...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2021· Phe Inc

Recalled Item: X RATED HONEY FOR MEN Recalled by Phe Inc Due to Marketed without an...

The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 0.5mg/1mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 0.5mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Akorn, Inc.

Recalled Item: Betamethasone Dipropionate Lotion USP (Augmented) Recalled by Akorn, Inc....

The Issue: Failed impurities/degradation specification: Out of Specification for an...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· SigmaPharm Laboratories LLC

Recalled Item: Sodium Phenylbutyrate POWDER Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Failed Impurities Specifications: Out of Specification impurity results...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 11, 2021· Ebay Seller - John Nguyen

Recalled Item: Hydro Pinapple Burn Max Health Thach Dua Recalled by Ebay Seller - John...

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
DrugAugust 10, 2021· SterRx, LLC

Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2021· SterRx, LLC

Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Non-Sterility: firm's third party lab confirmed microbial contamination.

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 6, 2021· XELLIA PHARMACEUTICALS USA, LLC

Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...

The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2021· XELLIA PHARMACEUTICALS USA, LLC

Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...

The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2021· Hikma Pharmaceuticals USA Inc.

Recalled Item: Bleomycin for Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Labeling: Not elsewhere classified: Mislabeling

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

Class III — Low RiskOngoing
Refund
DrugAugust 5, 2021· DuPont Nutrition USA, Inc

Recalled Item: Avicel Recalled by DuPont Nutrition USA, Inc Due to Out of specification...

The Issue: Out of specification results for conductivity.

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

Class III — Low RiskOngoing
Refund
DrugAugust 3, 2021· The Harvard Drug Group

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by The Harvard Drug Group Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund