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. 2,277 recalls have been distributed to Montana in the last 12 months.
Showing 44721–44740 of 48,326 recalls
Recalled Item: Benefiber Fiber Supplement Plus Calcium Recalled by Novartis Consumer Health...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Topical Oil (SCALP OIL) Recalled...
The Issue: Subpotent Drug: the active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lightning ROD capsules Recalled by Chang Kwung Products Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Lightning Rod capsules are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lightning ROD capsules Recalled by Chang Kwung Products Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Lightning Rod capsules are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: da Vinci 5 mm Instrument Cannulae for use with the Recalled by Intuitive...
The Issue: Intuitive Surgical is implementing a voluntary Field Action to implement a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci 5 mm Flared Instrument Cannulae for use with Recalled by Intuitive...
The Issue: Intuitive Surgical is implementing a voluntary Field Action to implement a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leucadia Autolok" Polyaxial Pedicle Screw System. Intended to help provide...
The Issue: Alphatec Spine initiated this medical device recall for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System (product code 6802783) Product Usage:...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Short Product Code:...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to There is evidence...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHO¿ Assay Software (OAS) Server Recalled by Ortho-Clinical Diagnostics...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Product...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Long Recalled...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System (product code 6802413) Product Usage: For...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With (2) Fixation Cannulae - 5mm Recalled...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Short...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.