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 43214340 of 13,375 recalls

DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2020· Teva Pharmaceuticals USA

Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...

The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2020· Teva Pharmaceuticals USA

Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...

The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2020· Strides Inc.

Recalled Item: Strides Pharma Inc.Potassium Chloride Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2020· Teva Pharmaceuticals USA

Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Sub-Potent Drug: Out of specification test results for potency (below...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2020· BAYSHORE PHARMACEUTICALS

Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by BAYSHORE...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2020· BAYSHORE PHARMACEUTICALS

Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by BAYSHORE...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2020· Mylan Institutional LLC

Recalled Item: Amiodarone Hydrochloride Injection Recalled by Mylan Institutional LLC Due...

The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 17, 2020· Maison Terre, LLC

Recalled Item: Goldenseal Root Powder Organic Recalled by Maison Terre, LLC Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA laboratory analysis...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 17, 2020· Mylan Institutional LLC

Recalled Item: Tranexamic Acid Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· Grupo Asimex de Mexico SA de CV

Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...

The Issue: CGMP Deviations: All other lots are being recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump Recalled...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· Grupo Asimex de Mexico SA de CV

Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...

The Issue: Chemical Contamination: FDA analysis found the product contains methanol,...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund