Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,716 recalls have been distributed to Louisiana in the last 12 months.
Showing 1841–1860 of 51,202 recalls
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: Sukhi's Recalled by Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian...
The Issue: Potential contamination with foreign objects (metal pieces).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sukhi's TIKKA MASALA CURRY PASTE Recalled by Jagpreet Enterprises, LLC. dba...
The Issue: Potential contamination with foreign objects (metal pieces).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sukhi's Recalled by Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian...
The Issue: Potential contamination with foreign objects (metal pieces).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sukhi's CLASSIC CURRY PASTE Recalled by Jagpreet Enterprises, LLC. dba...
The Issue: Potential contamination with foreign objects (metal pieces).
Recommended Action: Do not consume. Return to store for a refund or discard.
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.