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.

48,219 total recalls
2,540 in last 12 months

Showing 61816200 of 13,375 recalls

DrugNovember 6, 2018· L. Perrigo Company

Recalled Item: Antacid Tablets Recalled by L. Perrigo Company Due to Presence of foreign...

The Issue: Presence of foreign substance: Product found to contain metal particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2018· Breckenridge Pharmaceutical, Inc.

Recalled Item: Megestrol Acetate Oral Suspension Recalled by Breckenridge Pharmaceutical,...

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

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

Class III — Low RiskOngoing
Refund
DrugNovember 5, 2018· Kadesh International

Recalled Item: puriton EYE RELIEF DROPS Recalled by Kadesh International Due to...

The Issue: Non-Sterility: Product manufactured under non-sterile production conditions.

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Administration and Training Kits Recalled by Bound Tree...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Kit NOT FOR IV USE Recalled by Bound Tree Medical, LLC Due to...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling:...

The Issue: Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly...

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

Class III — Low RiskOngoing
Refund
DrugNovember 1, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp date: vials of epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Westminster Pharmaceuticals Llc

Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...

The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund