Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,400 recalls have been distributed to Montana in the last 12 months.
Showing 21561–21580 of 48,326 recalls
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...
The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...
The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Microtainer PSTTubes with LH (Lithium Heparin) Part/Catalog Number:365985...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer SST- Amber Part/Catalog Number: 365978 Recalled by Becton...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer SST Part/Catalog No.365967 Recalled by Becton Dickinson &...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer PST Tubewith LH (Lithium Heparin) - Amber Part/Catalog...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963 Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Tubes with FE (Sodium Fluoride / Disodium EDTA) Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974 Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promacta (eltrombopag) 12.5 mg for Oral Suspension Recalled by Novartis...
The Issue: Cross Contamination with Other Products: product is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol) Recalled by...
The Issue: Incorrect/undeclared excipients: Hand sanitizer was made using the wrong...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cadence Science Pressure Control Glass Syringe Recalled by Cadence Science,...
The Issue: The glass syringe used with Pressure Control Syringes may potentially break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex HUDSON RDI NEONATAL ConchaSmart Breathing Circuit with Dual Heated...
The Issue: Reported complaints of cracks being observed, prior to use, on swivel wye...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA RF IgM Well Recalled by Phadia Ab Due to Potential for reporting low...
The Issue: Potential for reporting low assay results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leadwire sets with snap ends: REF/Catalog Number Description 2106381-001 ECG...
The Issue: ECG trunk cables and leadwires may reduce the amount of energy reaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.