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. 2,530 recalls have been distributed to Montana in the last 12 months.
Showing 9281–9300 of 48,326 recalls
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM-Intended for knee Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat...
The Issue: The product contains an expired diluent vial. If the impacted product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL (UVSL) Command Module Recalled by Spacelabs Healthcare, Inc....
The Issue: Command modules will display the following when parameter processing is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Admelog Recalled by Sanofi-Aventis U.S. LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Malformed crimped collar seal
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: StealthStation Cranial Software Recalled by Medtronic Navigation, Inc. Due...
The Issue: During non-axial/some axial exams, software anomalies occur during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: Recalled by Bard...
The Issue: Coaxial cannula internal diameter and length of biopsy instruments exceed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL Recalled by SCA...
The Issue: Subpotent Drug: Out of specification results for low potency was obtained.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture...
The Issue: The Hard Line Chairside Reline Kit (570-0718) (0921940HS) was labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Over-Head Ceiling Tube Support Recalled by SHIMADZU CORPORATION MEDICAL...
The Issue: Eight fixing bolts at the base of the X-ray ceiling tube column assembly may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Vision Multi-Chamber Washer/Disinfector Recalled by Steris...
The Issue: In the remote occurrence in which the electrical contactor component present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical...
The Issue: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical...
The Issue: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole sodium for Injection 40 mg*/vial Recalled by Methapharm Inc Due...
The Issue: CGMP Deviations; The impacted product and lot number was inadvertently...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Savor Imports IQF Whole Raspberries Recalled by Mondi Lamex Serbia Due to...
The Issue: Potential contamination with Hepatitis A
Recommended Action: Do not consume. Return to store for a refund or discard.