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. 2,524 recalls have been distributed to Montana in the last 12 months.
Showing 10641–10660 of 48,326 recalls
Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm) Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter Product Code: 3420 Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm) Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Pak Surgical Procedure Pack Recalled by Alcon Research, LLC Due...
The Issue: Due to difficulty removing the liner on the adhesive components of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0. Used to display medical images (Including...
The Issue: There is the potential that after installation of the IAS tool, some studies...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer version 5.0. Used to display...
The Issue: There is the potential that after installation of the IAS tool, some studies...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE Recalled by...
The Issue: Upon review of its batch record, Southmedic identified that lot # W92761 was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic...
The Issue: Confirmed an average positive bias of 40% for testosterone concentrations of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrackX Insight Base Modular Instrument Tracker Recalled by Trackx Technology...
The Issue: The device is breaking and falling off the Nuvasive T-Handle with Hudson...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...
The Issue: The products may have the potential to burn customers. Firm has received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...
The Issue: The products may have the potential to burn customers. Firm has received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...
The Issue: The products may have the potential to burn customers. Firm has received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infection Control (IC) Lifting Strap used with the following Cirrus Recalled...
The Issue: Two customers reported four incidents in which the lifting strap broke while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Viatris Inc Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: Tablets exceeds specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1...
The Issue: Potential table stop due to a broken tabletop cable: On the ProxiDiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propel Mini Mometasone Furoate Sinus Implant Recalled by Intersect ENT, Inc....
The Issue: Sinus Implant product label displays incorrect product information...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplex HV With Gentamicin CE Recalled by Howmedica Osteonics Corp. Due to...
The Issue: Simplex HV With Gentamicin CE, 10 PACKS (P/N 6193-1-010) were distributed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Umami Everyday Savory Spice Recalled by Seed Ranch Flavor Co Due to...
The Issue: Three sauces contain undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.