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. 2,340 recalls have been distributed to Montana in the last 12 months.
Showing 35561–35580 of 48,326 recalls
Recalled Item: Iowa Select Herbs LLC Recalled by Iowa Select Herbs LLC Due to Pursuant to a...
The Issue: Pursuant to a consent decree for injunctive relief the recalling firm was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Iowa Select Herbs LLC Recalled by Iowa Select Herbs LLC Due to Pursuant to a...
The Issue: Pursuant to a consent decree for injunctive relief the recalling firm was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Iowa Select Herbs LLC Recalled by Iowa Select Herbs LLC Due to Pursuant to a...
The Issue: Pursuant to a consent decree for injunctive relief the recalling firm was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Beef Extract Powder Recalled by Acumedia Manufacturers, Inc. Due to...
The Issue: Incorrect expiration date on label. Correct expiration date was March 25,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack Recalled by...
The Issue: Dietary supplements contain low levels of undeclared boron
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Source Naturals Hydrogen Boost Capsule: 6 Count Trial Recalled by Threshold...
The Issue: Dietary supplements contain low levels of undeclared boron
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters. For intra-cardiac...
The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICroSTREP plus 2 Panel Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling MICroSTREP plus 1 and MICroSTREP plus 2 panels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carto 3 EP Navigation System. Electro physiology system which views Recalled...
The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 3.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICroSTREP plus 1 Panel Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling MICroSTREP plus 1 and MICroSTREP plus 2 panels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software Anomaly...
The Issue: Software Anomaly during ADD Installation on VITROS 5,1 FS Chemistry Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 8.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClomiPHENE CITRATE Tablets Recalled by EMD Serono, Inc. Due to Chemical...
The Issue: Chemical Contamination: impurity failure due to chemical contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Products Intended to be Sterile Recalled by Medistat RX L.L.C. Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bravelle 75 IU (urofollitropin for injection Recalled by Ferring...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorescence Imaging Procedure Kits used with the da Vinci Si Recalled by...
The Issue: B. Braun 2 gang 4-way stopcocks in the Fluorescence Imaging Procedure Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for...
The Issue: Incorrect tubing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.