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. 2,609 recalls have been distributed to Louisiana in the last 12 months.
Showing 15981–16000 of 29,201 recalls
Recalled Item: DigitalDiagnost Single Detector (Stitching Patient Support) 712020 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Recalled by Philips Medical Systems Gmbh, DMC Due to The...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips Medical Systems Gmbh, DMC Due to...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 (Stitching Patient Support) 712225 Recalled by Philips...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Upgrades (Stitching Patient Support) 712083 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: Recalled by...
The Issue: Genicon is providing updated IFU labeling to users to provide clarity on how...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitor with one Blood Parameter Module and one HSat Probe Recalled by...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood parameter monitoring system 500 H/SAT Recalled by Terumo...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT CLEARVUE isp Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Certain NAUTILUS DELTA Port Kit product code / lot number combinations may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M530 OHX Microscope System Supplied with 100 - 120 Vac. Recalled by...
The Issue: Recall is due to a design weakness of the power insert module.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This is an accessory to Intelect Advanced Recalled by DJO, LLC Due to The...
The Issue: The device accessories were not labeled with appropriate latex warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.