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. 2,548 recalls have been distributed to Montana in the last 12 months.
Showing 4901–4920 of 48,326 recalls
Recalled Item: Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013...
The Issue: Invalid Controls. The Low Control is out of range; too high which causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM...
The Issue: During the assembly of the FRT250 cartridge assembly, an incorrect component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine HCL Injection Recalled by TAILSTORM HEALTH INC Due to Subpotent...
The Issue: Subpotent Drug: reduced efficacy for epinephrine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2 Recalled by...
The Issue: It was confirmed that fibrinogen in patient plasma samples precipitates out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for...
The Issue: Devices were labeled with an expiration date of four years and ten days...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B-Intended to be used Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEG-3350 Recalled by Novel Laboratories, Inc. d.b.a Lupin Somerset Due to...
The Issue: Defective container: potential for non-sealed pouches which can lead to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Verapamil Hydrochloride Injection Recalled by Zydus Pharmaceuticals (USA)...
The Issue: Cross contamination with other products.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Verapamil Hydrochloride Injection Recalled by Zydus Pharmaceuticals (USA)...
The Issue: Cross contamination with other products.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Micafungin for injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Cross contamination with other products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Micafungin for injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Cross contamination with other products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Decitabine for Injection 50mg per vial Recalled by SUN PHARMACEUTICAL...
The Issue: CGMP Deviations: Out of Specification for Total Aerobic Microbial Count...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BioPince Ultra Full Core Biopsy Instrument: : 360-1080-01 Recalled by Argon...
The Issue: Holes have been identified in biopsy instrument packaging trays compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable 5 Lead Cable and Lead Wire System Recalled by Stryker...
The Issue: Disposable 5 lead cable and lead wire system package that should contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMINOS Lotus Max -Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max -Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max- Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.