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 34613480 of 48,215 recalls

DrugDecember 18, 2024· Granules Pharmaceuticals Inc.

Recalled Item: Colchicine Capsules 0.6 mg Recalled by Granules Pharmaceuticals Inc. Due to...

The Issue: Failed Dissolution Specifications: Out of specification observed during the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2024· Eugia US LLC

Recalled Item: medroxyPROGESTERone Acetate Injectable Suspension Recalled by Eugia US LLC...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2024· AvKARE

Recalled Item: Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% Moisturizing...

The Issue: LABELING: LABEL MIX-UP

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

Class III — Low RiskOngoing
Refund
DrugDecember 18, 2024· AvKARE

Recalled Item: Polyvinyl Alcohol Ophthalmic Solution 1.4% Recalled by AvKARE Due to...

The Issue: LABELING: LABEL MIX-UP

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 18, 2024· Instrumentation Laboratory

Recalled Item: HemosIL Heparin Calibrators Recalled by Instrumentation Laboratory Due to...

The Issue: Control indicating lower than expected quality control (QC) results and in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2024· Olympus Corporation of the Americas

Recalled Item: Olympus MAJ-891 Forceps/Irrigation Plug (Isolated Type). Model/Catalog...

The Issue: Potential for inadvertent retention of biomaterial when the reprocessing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2024· Tornier S.A.S.

Recalled Item: Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide Recalled by Tornier...

The Issue: The Pin Guide is being recalled because the metal tube may disassemble from...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2024· Encore Medical, LP

Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to 5R 16MM...

The Issue: 5R 16MM knee tibial insert package may contain knee tibial insert 3R 14MM...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2024· Braemar Manufacturing, LLC

Recalled Item: Monitoring Service Application (MSA). Software to process Recalled by...

The Issue: Not all Electrocardiogram (ECG) events received July 2022-July 2024 were not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugDecember 17, 2024· Amerisource Health Services LLC

Recalled Item: glipiZIDE Recalled by Amerisource Health Services LLC Due to Failed...

The Issue: Failed Dissolution Specifications:

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2024· SHOPPERS- PLAZA

Recalled Item: FOUZEE SugarLin HERBAL FORMULA capsules Recalled by SHOPPERS- PLAZA Due to...

The Issue: Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 16, 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
DrugDecember 16, 2024· SOMERSET THERAPEUTICS LLC

Recalled Item: Atropine Sulfate Ophthalmic Solution Recalled by SOMERSET THERAPEUTICS LLC...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2024· Augustine Temperature Management, LLC

Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...

The Issue: There is over-molding that stabilizes the connection between the cable and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Augustine Temperature Management, LLC

Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...

The Issue: There is over-molding that stabilizes the connection between the cable and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Augustine Temperature Management, LLC

Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...

The Issue: There is over-molding that stabilizes the connection between the cable and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Recalled...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) MTO Recalled by MEDLINE...

The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing