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. 2,498 recalls have been distributed to Montana in the last 12 months.
Showing 13301–13320 of 27,852 recalls
Recalled Item: Sterile Co-Flex NL 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex Med 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex NL 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGUIDE System with software build iGuide 2.2.0 Recalled by Elekta, Inc. Due...
The Issue: Potential for iGUIDE to incorrectly monitor the 3D position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-25 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage:...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-60 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-04 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Conducting solution product codes:3310-15 ACS - Product Usage:...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual-Sided Interhemispheric Recalled by Ad-Tech Medical Instrument...
The Issue: Supplemental information provided with devices indicates that the subdural...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Depth Electrodes Recalled by Ad-Tech Medical Instrument Corporation Due to...
The Issue: Supplemental information provided with devices indicates that the subdural...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skull Anchor Bolts Recalled by Ad-Tech Medical Instrument Corporation Due to...
The Issue: Supplemental information provided with devices may indicate that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LSB Style Anchor Bolt. Labeled with the following parts: 13mm Recalled by...
The Issue: On June 12, 2019 Ad-Tech was made aware that on three different occasions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato...
The Issue: Discrepant length; Lot B88751 90mm screws were manufactured with a 100mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Precision Integrated System 120V & LEEP Precision Generator Recalled by...
The Issue: The products' cut, coagulate, or blend function may not operate with the use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Surgical System Recalled by Intuitive Surgical, Inc. Due to One da...
The Issue: One da Vinci Xi Endoscope Controller in the field was improperly calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products GLU Slides-Product Code:1707801. IVD VITROS...
The Issue: Potentially Biased Results using VITROS Chemistry Products GLU Slides
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.