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. 2,271 recalls have been distributed to Montana in the last 12 months.
Showing 45701–45720 of 48,326 recalls
Recalled Item: Well at Walgreens Wal-Tussin CF Max Recalled by Aaron Industries Inc Due to...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MET-Rx EXTREME NOS PUMPED NITRO-PUNCH Naturally Flavored DIETARY SUPPLEMENT...
The Issue: The color, odor, and taste of the products are changing and do not meet the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MET-Rx EXTREME NOS PUMPED DOUBLE BERRY Naturally and Artificially Flavored...
The Issue: The color, odor, and taste of the products are changing and do not meet the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MET-Rx EXTREME NOS PUMPED WATERMELON Naturally and Artificially Flavored...
The Issue: The color, odor, and taste of the products are changing and do not meet the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Elekta Recalled by Elekta, Inc. Due to If the Apex collimator is incorrectly...
The Issue: If the Apex collimator is incorrectly installed on the radiation head, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Bipolar Generator Foot Pedal Recalled by Aesculap, Inc. Due to The...
The Issue: The bipolar energy did not stop after release of the foot pedal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chenica Gunnell Rehab Series of Wheelchairs (GRSW) Recalled by CHENICA INC....
The Issue: The wheelchairs may not meet the specifications of WC-19 (crash testing),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Recalled by St Jude Medical Inc Due to The distal end of...
The Issue: The distal end of the core wire of the TorqVue FX Delivery System could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and...
The Issue: Microbial Contamination of Non-Sterile Product(s): The product has the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tausi Brand Salted Black Beans Recalled by Walong Marketing, Inc. Due to...
The Issue: Walong is recalling Tausi Brand Salted Black Beans because it may have the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SybronEndo Replacement AC Power Cord Recalled by Ormco/Sybronendo Due to A...
The Issue: A recall has been issued by SybronEndo because a Canadian Standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SybronEndo Elements Obturation Unit Recalled by Ormco/Sybronendo Due to A...
The Issue: A recall has been issued by SybronEndo because a Canadian Standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK INSIGHT DENTAL FILM in SureSoft Packets Recalled by Carestream Health,...
The Issue: Missing symbols and manufacturing information on the clear carton label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Product exceeds specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips BuckyDiagnost Radiographic. Catalog Numbers: 704031 Recalled by...
The Issue: An inspection of IATD (Installation Acceptance Test Document)IA SID (Source...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...
The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips BuckyDiagnost Radiographic Recalled by Philips Healthcare Inc. Due...
The Issue: An inspection shows several IATDs (Installation Acceptance Test could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...
The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phillips Easy Diagnost Eleva DRF. Model Number: 706034 Product Usage:...
The Issue: The mirror icon on the bottom of each image could be misinterpreted as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iconos R200 C20 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens has become aware of a potential malfunction and possible hazard to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.