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 22681–22700 of 48,326 recalls
Recalled Item: COBRA FUSION 150 Ablation System Recalled by AtriCure, Inc. Due to There is...
The Issue: There is a potential for patients undergoing ablation to experience an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT scanners Product Usage: The system is intended for head...
The Issue: Additional low dose radiation exposure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Recalled...
The Issue: Cosmetic Kit was packaged with a mislabel medical product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irbesartan Tablets 300 mg 90 count Rx only Manufactured by: Recalled by...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and HydrochlorothiazideTablets Recalled by Prinston...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine HCl Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: Related compound results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: Failed Impurities/Degradation Specifications: Elevated levels of a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: Recalled by...
The Issue: On-X Valve was mislabeled with the incorrect serial number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipid Panel test strips Recalled by Polymer Technology Systems, Inc. Due to...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHOL+HDL+GLU test strips Recalled by Polymer Technology Systems, Inc. Due to...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences(R) IntraClude(TM) Intra-Aortic Occlusion Device is a...
The Issue: Edwards Lifesciences has received a limited number of customer reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipid Panel test strips (as a component of smart bundles) Recalled by...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF) Recalled by KRS...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF) Recalled by KRS...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by LUPIN SOMERSET Due to...
The Issue: Failed Impurities/Degradation Specifications: Expansion of October 2018...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: infants* IBUPROFEN Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.