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. 2,646 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,646 in last 12 months

Showing 1204112060 of 29,201 recalls

Medical DeviceApril 17, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Image-Intensified Fluoroscopic X-Ray System Recalled by Siemens...

The Issue: The unplugging of the main cable on the monitor trolley from the X10...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Knee Products: 183742 Vanguard Knee System Recalled by Biomet, Inc. Due to...

The Issue: Potential presence of elevated endotoxin levels that exceed the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2020· Becton Dickinson & Company

Recalled Item: BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553)...

The Issue: This product has been confirmed to exhibit holes in the packaging, which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2020· Elekta Inc

Recalled Item: Elekta MONACO RTP Sytem Recalled by Elekta Inc Due to The Monaco RTP...

The Issue: The Monaco RTP Radiation Treatment Planning System may change the shape and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2020· C.R. Bard Inc

Recalled Item: SureStep Foley Tray System - Product Usage: Intended for use Recalled by...

The Issue: There is potential for a white paper-type residue attached to the catheter.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2020· Becton Dickinson & Co.

Recalled Item: BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Recalled by...

The Issue: May exhibit increased levels of artifacts which could be difficult to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2020· Becton Dickinson & Co.

Recalled Item: BD BBLTM Gram Crystal Violet 3.8L-- IVD Primary stain for Recalled by Becton...

The Issue: May exhibit increased levels of artifacts which could be difficult to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2020· Becton Dickinson & Co.

Recalled Item: BD BBLTM Gram Stain Kit with Stabilized Iodine-- IVD For Recalled by Becton...

The Issue: May exhibit increased levels of artifacts which could be difficult to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Philips North America, LLC

Recalled Item: Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The...

The Issue: The labeling of the Philips Chest Pneumograph does not include a statement...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing