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. 2,481 recalls have been distributed to Louisiana in the last 12 months.
Showing 36541–36560 of 51,202 recalls
Recalled Item: Synaptive Medical BrightMatter Navigator System (Guide System). Part number...
The Issue: Out of tolerance for radio frequency emissions. At the 150-1000MHz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo Humidifier 163 Recalled by Teleflex Medical Due to Cracks may occur at...
The Issue: Cracks may occur at the 15mm and 22mm ISO female connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gynecare Thermachoice III Uterine Balloon Therapy System Ethicon Recalled by...
The Issue: Stability data does not substantiate the labeled two-year shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS300 radiographic Cassette Holder or Wall Stand. For use in Recalled by Del...
The Issue: The wall stand cassette holder can suddenly fall to the bottom of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Position Pro Mattress. Mattress Recalled by Stryker Medical Division...
The Issue: Potential for power cord to melt; hazards include electric shock and fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS200 radiographic Cassette Holder or Wall Stand. For use in Recalled by Del...
The Issue: The wall stand cassette holder can suddenly fall to the bottom of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion Recalled...
The Issue: There have been intermittent issues with Supercap POST (power on self-test)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIPO ESCULTURA capsules Recalled by Lipo Escultura Corp. Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norpace CR (disopyramide phosphate) extended-release capsules USP Recalled...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...
The Issue: The item was recalled due to an increased user/patient risk of exposure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Green Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...
The Issue: There may be a separation and an insufficient weld between the spring and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal Standard Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...
The Issue: There may be a separation and an insufficient weld between the spring and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.