Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,614 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,614 in last 12 months

Showing 941960 of 13,381 recalls

DrugAugust 9, 2024· Direct Rx

Recalled Item: Ibuprofen 800mg Recalled by Direct Rx Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: Product failed impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Testosterone Gel Recalled by Teva Pharmaceuticals USA, Inc Due to...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU Ibuprofen Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed impurities/degradation specifications: results for unknown impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU Ibuprofen Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed impurities/degradation specifications: results for unknown impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU Ibuprofen Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed impurities/degradation specifications: results for unknown impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2024· Zeco LLC

Recalled Item: Rubbing Alcohol (70% Isopropyl Alcohol) Recalled by Zeco LLC Due to CGMP...

The Issue: CGMP Deviations: sterile water not used for production

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2024· Zeco LLC

Recalled Item: HAND-I-SAN Recalled by Zeco LLC Due to CGMP Deviations: sterile water not...

The Issue: CGMP Deviations: sterile water not used for production

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2024· EMPOWER CLINIC SERVICES LLC

Recalled Item: Empower Pharmacy Recalled by EMPOWER CLINIC SERVICES LLC Due to Lack of...

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 1, 2024· Baxter Healthcare Corporation

Recalled Item: Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection) Recalled by...

The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 1, 2024· Amneal Pharmaceuticals, LLC

Recalled Item: Methotrexate Tablets Recalled by Amneal Pharmaceuticals, LLC Due to Presence...

The Issue: Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate...

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

Class III — Low RiskOngoing
Refund
DrugJuly 31, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Indomethacin Extended-Release Capsules Recalled by Glenmark Pharmaceuticals...

The Issue: Failed Dissolution Specifications: below specification results

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 31, 2024· Granules Pharmaceuticals Inc.

Recalled Item: Gabapentin Tablets Recalled by Granules Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2024· Eugia US LLC

Recalled Item: Progesterone Injection Recalled by Eugia US LLC Due to Presence of...

The Issue: Presence of Particulate Matter: Complaint received of a glass particle in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2024· B. Braun Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 23, 2024· FDC Limited

Recalled Item: Ciprofloxacin ophthalmic solution USP Recalled by FDC Limited Due to...

The Issue: Defective container: unable to get the solution out of the bottle as the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Glenmark Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2024· FDC Limited

Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...

The Issue: Defective container; yellow colored spike from cap lodged in the nozzle

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2024· MAIN PRODUCTS INC

Recalled Item: Umary Acido Hialuronico Recalled by MAIN PRODUCTS INC Due to Undeclared...

The Issue: Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2024· Supercore Products Group Inc.

Recalled Item: Gold Hard Steel Plus Liquid Recalled by Supercore Products Group Inc. Due to...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2024· Supercore Products Group Inc.

Recalled Item: Hard Steel Capsules packaged in 1 count blister packs in boxes of 10...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...

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

Class I — Serious Health HazardOngoing
Refund