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 8981–9000 of 29,201 recalls
Recalled Item: Artis Q biplane with software VD12-angiography systems developed for single...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor with software VD12-angiography systems developed for single...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee ceiling with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen biplane with software VD12- angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q ceiling with software VD12-angiography systems developed for single...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen floor with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee multi-purpose with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspiration Syringe Kit Recalled by MICROVENTION INC. Due to Syringe Kits...
The Issue: Syringe Kits labeled for distribution OUS were inadvertently shipped to US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nimbus PainPro Ambulatory Infusion Pumps with software version v4 Recalled...
The Issue: An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model B35200 - Percept PC BrainSense Implantable Neurostimulator Recalled by...
The Issue: During cardioversion events, the Model B35200 Percept PC Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas u 601 urinalysis test system Recalled by Roche Diagnostics Operations,...
The Issue: A potential risk for false negative nitrite results exists when endogenous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz Udel Sterilization Tray Instructions for Use Recalled by Karl...
The Issue: To ensure sterilization effectiveness, sterilization tray instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freelite Human Lambda Free Kit (for use on the SPAPLUS) Recalled by The...
The Issue: Due to calibration curves producing a higher activity than routinely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Centricity Universal Viewer Zero Footprint Client Recalled by GE...
The Issue: There is a potential to display incomplete patient imaging study.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT...
The Issue: During stent graft deployment, the spindle may detach from the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.