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. 1,023 recalls have been distributed to Idaho in the last 12 months.
Showing 17461–17480 of 48,215 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health"...
The Issue: The third-party brand latex micro surgical gloves packaged within specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...
The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...
The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) Recalled by...
The Issue: Opticross 35 Peripheral Imaging Catheter is being recalled because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imactis Patient Fiducial (Patient ) Recalled by Imactis Due to The firm has...
The Issue: The firm has received reports concerning the patient fiducial disk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm....
The Issue: Exactech is recalling the Equinoxe Reverse Shoulder Compression...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm....
The Issue: Exactech is recalling the Equinoxe Reverse Shoulder Compression...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 In. Flat Responder Emergency Trauma Dressing part number 30-0171 Recalled...
The Issue: Lack of sterility assurance of the 30-0171
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwiftHook sold as the following: a. Individually as SwiftHook b. Recalled by...
The Issue: Carry bar may detach during use of mobile lifts and ceiling lifts equipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.