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. 2,568 recalls have been distributed to Montana in the last 12 months.
Showing 1781–1800 of 48,326 recalls
Recalled Item: Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name:...
The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...
The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name:...
The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...
The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Recalled by THOR...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlantis IO FLO Product Name: Atlantis IO FLO-S Recalled by...
The Issue: The defect in the thread area will not allow the device to fully engage with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Recalled by...
The Issue: The defect in the thread area will not allow the device to fully engage with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Recalled by THOR...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOTAK RELIANCE G/SG with 4-SITE Connector Recalled by Boston Scientific...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELIANCE 4-FRONT Recalled by Boston Scientific Corporation Due to Affected...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOTAK RELIANCE G/SG Recalled by Boston Scientific Corporation Due to...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: An out-of-Specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Model RXM1000 UDI Codes: (01)00860003983812(11)230504(21)X11001...
The Issue: Due to incorrect software configuration that potentially allows more than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bartels ELISA Legionella Urinary Antigen. Model Number: B1029-440. In Vitro...
The Issue: Potential for Bartels ELISA Legionella Urinary Antigen kit B1029-440 lot 065...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories,...
The Issue: Failed Dissolution Specifications: low dissolution results
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.