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. 2,498 recalls have been distributed to Montana in the last 12 months.
Showing 12201–12220 of 48,326 recalls
Recalled Item: Replacement back up batteries distributed on or after April 1 Recalled by GE...
The Issue: Insufficient battery backup power resulting in premature shutdown of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Back up batteries in Ventilators labeled as the following: a. Recalled by GE...
The Issue: Insufficient battery backup power resulting in premature shutdown of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: progenamatrix Human Keratin Matrix Recalled by ProgenaCare Due to Inner...
The Issue: Inner pouch seal may be inadequate resulting in lack of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium & Hydrochlorothiazide Tablets Recalled by Macleods Pharma...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Oral Topical Solution Recalled by Akorn, Inc. Due to...
The Issue: Failed viscosity specification - product was below specificcation
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium & Hydrochlorothiazide Tablets Recalled by Macleods Pharma...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium & Hydrochlorothiazide Tablets Recalled by Macleods Pharma...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine 2.5% and Prilocaine 2.5% Cream Recalled by Teva Pharmaceuticals...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Devices...
The Issue: Devices were subject to unapproved rework processes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Medtronic Inc Due to The pump...
The Issue: The pump may have a welding defect that can lead the pump to malfunction....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 ToRC IgM Reagent Pack Recalled by Bio-Rad Laboratories, Inc....
The Issue: Performance concerns for the CMV IgM analyte. Analyte has demonstrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe Recalled by...
The Issue: Patient chart label contains incorrect Part Number and volume amount.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epinephrine Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due...
The Issue: cGMP deviations: Temperature abuse
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proventil HFA Recalled by Mckesson Medical-Surgical Inc. Corporate Office...
The Issue: cGMP deviations: Temperature abuse
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thrombin JMI Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due...
The Issue: cGMP deviations: Temperature abuse
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefazolin for injection USP Recalled by Mckesson Medical-Surgical Inc....
The Issue: cGMP deviations: Temperature abuse
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duraclon (clonidine HCl injection Recalled by Mckesson Medical-Surgical Inc....
The Issue: cGMP deviations: Temperature abuse
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.