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. 909 recalls have been distributed to Montana in the last 12 months.
Showing 44601–44620 of 48,326 recalls
Recalled Item: Stryker Instruments 0400-830-000 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-850-000 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sovereign¿ Compact Phacoemulsification System Recalled by Abbott Medical...
The Issue: Abbott Medical Optics Inc. (AMO) initiated this Urgent Notice of Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Large Nonsterile...
The Issue: This is a recall expansion from the 2010 recall which now includes seven...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Small Nonsterile...
The Issue: This is a recall expansion from the 2010 recall which now includes seven...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mother Earth Products Recalled by Mother Earth International LLC Due to...
The Issue: The product was manufactured with a Soy Protein Isolate manufactured by CHS,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pinook Micro Massager Distributed by www.pinookusa.com Used to strengthen...
The Issue: Failure to submit a premarket submission and gain approval of a medical device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen...
The Issue: Failure to submit a premarket submission and gain approval of a medical device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to Lack...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Folic Acid Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection Recalled by Baxter...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nimodipine Capsules 30 mg Recalled by Sun Pharmaceutical Industries Inc. Due...
The Issue: Crystallization; crystallized nimodipine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride and 5% Dextrose Injection Recalled by Baxter...
The Issue: Lack of Assurance of Sterilty: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zolpidem Tartrate Tablets 5 mg Recalled by American Health Packaging Due to...
The Issue: Unit Dose Mispackaging: This recall event is due to a random undetected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to leaking pouches
The Issue: leaking pouches
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...
The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...
The Issue: There is a possibility that the pump head was not shipped in the locked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.