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. 2,535 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,535 in last 12 months

Showing 73017320 of 13,375 recalls

DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Stanozolol USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Testosterone USP (Micronized) (Yam) for prescription compounding Recalled by...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Sumatriptan Succinate USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 7, 2018· Pfizer Inc.

Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...

The Issue: Non-Sterility: Confirmed customer complaints of glass product container...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 7, 2018· Pfizer Inc.

Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...

The Issue: Non-Sterility: Confirmed customer complaints of glass product container...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 5, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Azelastine HCl Nasal Solution (Nasal Spray) 0.1% (137 mcg per spray)...

The Issue: Sun Pharmaceutical is recalling Azelastine HCl Nasal Solution, 0.1% (30 mL...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2018· ALLERGAN

Recalled Item: NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets Recalled by...

The Issue: Labeling: Not Elsewhere Classified: does not have the required "CII"...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2018· Aurobindo Pharma Ltd.

Recalled Item: Metformin Hydrochloride Tablets Recalled by Aurobindo Pharma Ltd. Due to...

The Issue: Presence of Foreign Tablet: Metformin BP 1000mg was found in bottle of...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2018· Millennium Pharmaceuticals Inc.

Recalled Item: VELCADE (bortezomib) for injection Recalled by Millennium Pharmaceuticals...

The Issue: Defective Container: Confirmed reports of loose vial crimps.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 40 mg Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 75 mcg/h Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 10 mg Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Mckesson Packaging Services

Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Packaging Services...

The Issue: Subpotent Drug: Out of specification for assay (stability testing)

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 25 mcg/h Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 20 mg Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel (flavocoxid 500 mg) capsules Recalled by Primus Pharmaceuticals,...

The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel500 (flavocoxid and citrated zinc bisglycinate) 500 mg/50 mg capsules...

The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel (flavocoxid 250 mg) capsules Recalled by Primus Pharmaceuticals,...

The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...

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

Class I — Serious Health HazardOngoing
Refund