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. 2,678 recalls have been distributed to Louisiana in the last 12 months.
Showing 8561–8580 of 29,201 recalls
Recalled Item: RayStation 4-11B Recalled by RaySearch America Inc Due to Incorrect source...
The Issue: Incorrect source to skin or surface distance (SSD) calculation may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Integrated Reaction Units (IRU) Recalled by Abbott Molecular, Inc....
The Issue: There is potential for the Reaction Vessels (RVs) detaching from the RV cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS CMV IgM Recalled by bioMerieux, Inc. Due to Invalid calibrations (out...
The Issue: Invalid calibrations (out of range high) while using the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Fructosamine (Fruc) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Calcium_2 (CA_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultima Activator II Reusable Drive Mechanism Recalled by Maquet...
The Issue: Potential for corrosion on the pins of the Ultima Activator II Reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 SYPH T PACK Syphilis Total & RPR Reagent Pack Recalled by...
The Issue: Due to current concerns related to COVID-19 vaccine interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Syphilis Total & RPR Calibrator Set CAL Recalled by Bio-Rad...
The Issue: Due to current concerns related to COVID-19 vaccine interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The IFU for the Autoclavable Temperature Probes: Part # 453564635891...
The Issue: Update to instructions for use regarding the cleaning and disinfection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brius Patient Specific Brackets (components in a set of custom Recalled by...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Customized Brius Appliances (custom metal orthodontic devices) Recalled by...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brius Pontics (components in a set of custom metal orthodontic devices)...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...
The Issue: There is a potential for AED pads to experience gel separation from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.