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 22701–22720 of 48,326 recalls
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: Ezetimibe and Simvastatin Tablets 10mg/80 mg Recalled by Dr. Reddy's...
The Issue: Presence of Foreign Substance: Product complaint of black speckles observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proximal Humerus Plate Recalled by Miami Device Solutions, LLC. Due to Right...
The Issue: Right Proximal Humerus Plates. Product component parts MDS130108R, may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm FDR Go PLUS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...
The Issue: FUJIFILM Medical Systems U.S.A., Inc., Modality Systems became aware of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit Recalled by Westmed, Inc. Due...
The Issue: A repair was made to an adapter mold resulting in parts being produced with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Neonatal Mask Recalled by...
The Issue: A repair was made to an adapter mold resulting in parts being produced with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask Recalled by...
The Issue: A repair was made to an adapter mold resulting in parts being produced with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIMADZU MobileDaRt Evolution (MX8 Version) Recalled by Shimadzu Medical...
The Issue: In these units, the brake is usually released by gripping the drive handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use Recalled by...
The Issue: False negative results with the BD MAX Extended Enteric Bacterial Panel when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is...
The Issue: Normal operation of the device is to power up the device in the morning,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Burr Recalled by Arthrex, Inc. Due to Devices may generate excessive...
The Issue: Devices may generate excessive heat during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH CARE Premium Drain bag Recalled by Teleflex Medical Due to The device...
The Issue: The device labels are not UDI compliant. The missing UDI compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRINIAS for diagnostic imaging and interventional procedures in cardiac...
The Issue: Two issues: Event 1: Normal operation of the device is to power up the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Urinary Drainage bag Recalled by Teleflex Medical Due to The device...
The Issue: The device labels are not UDI compliant. The missing UDI compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethyl Alcohol Enzymatic Assay Recalled by Lin-Zhi International Inc Due to...
The Issue: Shelf life of the product may be reduced due to degradation of the assay.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: aap Implante AG Recalled by AAP Implantate Ag Due to There is the potential...
The Issue: There is the potential for the Lambotte chisel to break at the welded piece...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: El Guapo Chile Habanero Habanero Chili Pepper 0.5oz Recalled by McCormick &...
The Issue: Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: El Guapo Pasilla-Ancho Chile Pods 2oz Recalled by McCormick & Company, Inc....
The Issue: Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Losartan Potassium Tablets Recalled by MAJOR PHARMACEUTICALS Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...
The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.