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. 1,908 recalls have been distributed to Montana in the last 12 months.
Showing 10381–10400 of 27,852 recalls
Recalled Item: Pinnacle Cups Recalled by DePuy Orthopaedics, Inc. Due to Certain Pinnacle...
The Issue: Certain Pinnacle Cup devices may potentially exhibit an oversized "minor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAHL 4212 HEATED MASSAGER Recalled by Wahl Clipper Corp Due to The...
The Issue: The connection between the massager and heat element can overheat causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Recalled by...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 Reperfusion Catheter The Penumbra JET Recalled by Penumbra...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yukon Polyaxial Screw Size 4.0x26mm (catalog number 7601-04026) Recalled by...
The Issue: The Yukon polyaxial screw used in the Yukon Spinal System was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENOVO Venous Stent System 8F Product Description(REF)/dimension: VENEL10040...
The Issue: Reports of the proximal end of the stent not immediately expanding upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuroreader Medical Image Processing Software - Product Usage: intended to...
The Issue: The Neuroreader has been distributed with a normative database that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA dsDNA Well - Product Usage: intended for the In-Vitro Recalled by...
The Issue: Decreased values for EliA ANA Positive Control when using the EliA dsDNA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENOVO Venous Stent System 9F Product Description(REF)/dimension: VENEL14040...
The Issue: Reports of the proximal end of the stent not immediately expanding upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENOVO Venous Stent System 10F Product Description(REF)/dimension:...
The Issue: Reports of the proximal end of the stent not immediately expanding upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use...
The Issue: Mislabeled product-Bactiseal Ventricular Catheter with Bactiseal Shunt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRYTIME MEDICAL REBOA Catheter Introducer Kit Recalled by Prytime Medical...
The Issue: There is a potential that a catheter convenience set contains a 21G access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bactiseal Ventricular Catheter with Bactiseal Shunt System - Product Usage:...
The Issue: Mislabeled product-Bactiseal Ventricular Catheter with Bactiseal Shunt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CKMB Slides: (1)VITROS CKMB Slides (60 Slide...
The Issue: VITROS Chemistry Products CKMB Slides Potential for Falsely Elevated Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERITAS Collagen Matrix - Product Usage: intended for use in Recalled by...
The Issue: VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Vision Single-Chamber Washer/Disinfector - Product Usage: intended...
The Issue: The electrical contactor component present in the drying chamber of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FUJIFILM Synapse PACS Software: versions 7.0.0 and 7.0.1 - Product Recalled...
The Issue: The software does not update measurements and calculations in the Clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment Delivery System with iDMS - Product Usage: used...
The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.