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. 2,548 recalls have been distributed to Montana in the last 12 months.
Showing 4841–4860 of 27,852 recalls
Recalled Item: The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence Recalled by...
The Issue: One lot of the Sofia 2 Flu + SARS Antigen FIA (Lot 709083) was labelled with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. HeartMate Touch Communication System Recalled by Thoratec Corp. Due to...
The Issue: Due to software and controller systems that results in unexpected pump start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270 Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova. Model (REF) Numbers 781172. Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX. Model (REF) Numbers 781271 Recalled by Philips North...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T. Model (REF) Numbers 781196 Recalled by Philips North America...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva XR. Model (REF) Numbers 781153 Recalled by Philips North America Due...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Initial system. Model (REF) Numbers 781178. Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX. Model (REF) Numbers 781262 Recalled by Philips North...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T. Model. (REF) Numbers 781277 Recalled by Philips North America...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera Achieva 1.5T Pulsar. Model (REF) Number 781171. Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion. Model (REF) Numbers 781346 Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173. Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T. Model (REF) Numbers 781260 Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Framegrabber card may not perform as intended. Monitor may show no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Framegrabber card may not perform as intended. Monitor may show no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Disk Bay may not perform as intended. System may stop functioning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Disk Bay may not perform as intended. System may stop functioning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3:1 Dermacarrier Recalled by Zimmer Surgical Inc Due to Due to manufacturing...
The Issue: Due to manufacturing issue, the product is labeled as 3:1 ratio, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.