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. 1,039 recalls have been distributed to Montana in the last 12 months.
Showing 15341–15360 of 48,326 recalls
Recalled Item: Starwest Botanicals Item#: 209617-34 Recalled by Starwest Botanicals, Inc...
The Issue: Presence of E. coli species
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DirectInject consists of a sterile dual paste system which is Recalled by...
The Issue: Inability for the user to inject the paste from the syringe into the target...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranberg MR Stylet Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Wheelchair Recalled by Merits Holdings Co. dba Merits Health Products,...
The Issue: Seat baseplate pin has broken in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scooter Recalled by Merits Holdings Co. dba Merits Health Products, Inc. Due...
The Issue: Seat baseplate pin has broken in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranberg MR Cannula Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranberg Laser Applicator Non-cooled Recalled by CLINICAL LASERTHERMIA...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Itraconazole Capsules Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Riomet (metformin hydrochloride oral solution) 500 mg/5 mL Cherry Flavor...
The Issue: Microbial Contamination of Non-Sterile Product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMPERIAL GOLD 2000 Recalled by QMart Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guanfacine Extended-Release Tablets 2 mg Recalled by Apotex Corp. Due to...
The Issue: Cross Contamination with Other Product: Product is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imperial Platinum 2000 Recalled by QMart Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZen Extreme 3000 Recalled by QMart Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Burro en Primavera Recalled by QMart Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD Recalled by Smiths Medical ASD Inc....
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 280 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palm Cups - Product Usage: intended to be used to Recalled by Smiths Medical...
The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftCytogenetics Recalled by Soft Computer Consultants, Inc. Due to Software...
The Issue: Software is given wrong results going out to HIS on test that had reruns.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR Recalled by...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.