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. 2,400 recalls have been distributed to Montana in the last 12 months.
Showing 21541–21560 of 48,326 recalls
Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA Recalled by Covidien LLC...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 CURVED TIP ART MED THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC Recalled by Covidien LLC...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA Recalled by Covidien LLC...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA45 CT AR MD THK REL Recalled by Covidien LLC Due to The device may be...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Senographe Pristina - Product Usage: Senographe Pristina generates...
The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Pristina Serena - Product Usage: Pristina Serena is an Recalled by GE...
The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0 Is a device that displays medical Recalled...
The Issue: There is the possibility of viewing studies directly from the Enterprise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS Foundation Centricity PACS software product is intended for...
The Issue: There is the possibility of viewing studies directly from the Enterprise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immulox Recalled by APS BioGroup, Inc Due to The recall is being conducted...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DPS Throat Spray Recalled by APS BioGroup, Inc Due to The recall is being...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Viralox Recalled by APS BioGroup, Inc Due to The recall is being conducted...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Immuno PRP Spray Recalled by APS BioGroup, Inc Due to The recall is being...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 45cm Shaft PRODUCT CODE: NSLX145C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 37cm Shaft PRODUCT CODE: NSLX137C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InterStim(TM) System Recalled by Medtronic Neuromodulation Due to There is a...
The Issue: There is a potential for an unexpected increase in stimulation during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntraClude Intra-Aortic Occlusion Device Recalled by Edwards Lifesciences,...
The Issue: Possibility of balloon rupture in intra-aortic occlusion devices. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.