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. 2,526 recalls have been distributed to Montana in the last 12 months.
Showing 10121–10140 of 27,852 recalls
Recalled Item: Digitial Medica X-ray Imagining System Recalled by Shanghai United Imaging...
The Issue: There is a potential for the X-Ray tube head (Touch screen interface) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular...
The Issue: Test results from the manufacturing line found a piece of damaged o-ring in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Band Recalled by G & H Wire Company Due to The text on the patient pack is...
The Issue: The text on the patient pack is correct and the product itself remains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible...
The Issue: The affected Milex Gellhorn pessaries were incorrectly manufactured with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions Ethicon Endo-Surgery Recalled by Stryker...
The Issue: Product was distributed without receiving regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartspan Transseptal Needles Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The labeled needle tip curvature of specific lots of transseptal needles may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSpan Transseptal Needles Catalog No. FND-019-01 Recalled by Merit...
The Issue: The labeled needle tip curvature of specific lots of transseptal needles may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...
The Issue: Non-sterile product was shipped to customers labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator Single-Use Polypectomy Snares Recalled by Boston Scientific...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator II Single-Use Polypectomy Snares Outer box UPN Recalled by Boston...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM...
The Issue: Distributed COVID test kits without emergency use authorization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tube Tracheostomy and Tube Cuff Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Smiths Medical became aware that three lot numbers of a specific model of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 6F Launcher Guide Catheter 100cm EBU 3.75 Model Number: LA6EBU375...
The Issue: Sterility may be compromised due to an unsealed pouch
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30...
The Issue: Sterility may be compromised due to an unsealed pouch
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.