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. 1,900 recalls have been distributed to Montana in the last 12 months.
Showing 13161–13180 of 48,326 recalls
Recalled Item: Mucus Relief D Recalled by Dr. Reddy's Laboratories, Inc. Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam Recalled by Ingenus Pharmaceuticals Llc Due to...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brownie Points Schmurtle 2oz Packaged in food grade cellophane only Recalled...
The Issue: Contains Statement on Label does not include all allergens - Peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg...
The Issue: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobazam Oral Suspension 2.5 mg/mL Recalled by VistaPharm, Inc. Due to...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mimvey (estradiol and norethindrone acetate tablets USP) Recalled by Teva...
The Issue: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arcos Modular Revision Hip System Recalled by Biomet, Inc. Due to The...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NavitrackER Kit A: Knee Recalled by Orthosoft, Inc. dba Zimmer CAS Due to...
The Issue: The product was released for distribution without passing sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Luer Lok Access Device - intended as a sterile Recalled by...
The Issue: May shed contaminant particles into the urine specimen that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayfare Dairy Free Butter Salted & Whipped Recalled by WayFare Health Foods,...
The Issue: Product showed suspected mold growth prior to expiration date.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenia Elition X (Product Number 781358) - HA FlexTrak II Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.