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. 2,716 recalls have been distributed to Louisiana in the last 12 months.
Showing 1781–1800 of 29,201 recalls
Recalled Item: Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit...
The Issue: Adapters may disconnect during setup or while in use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis HPCA Ambulatory Infusion Pump Recalled by Smiths Medical ASD,...
The Issue: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis VIP Ambulatory Infusion Pump Recalled by Smiths Medical ASD, Inc....
The Issue: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT Recalled by...
The Issue: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis Infusion Pump Models: 1) PUMP KIT Recalled by Smiths Medical ASD,...
The Issue: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Solis HSPCA Pump Recalled by Smiths Medical ASD, Inc. Due to Pumps may...
The Issue: Pumps may experience Wireless Connection Modules intermittent connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blueprint Software Recalled by Tornier S.A.S. Due to A software bug in...
The Issue: A software bug in Blueprint version 4.2.1 prevents users from accessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Sterile Weitlaner Retractor 3 x 4 Prong Recalled by MEDLINE...
The Issue: Three is the potential for the retractors to puncture through the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: Four (4) total reports were sent to customers with clinically relevant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Sterile Weitlaner Retractor Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Three is the potential for the retractors to puncture through the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487...
The Issue: Due to a software issue, the software may incorrectly process the date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artix MT Thrombectomy Device Recalled by Inari Medical - Oak Canyon Due to...
The Issue: Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Cardiovascular software versions 6.x Recalled by Philips...
The Issue: An issue was identified with the software when using the Echo Module of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as...
The Issue: Disconnection of the adapter from the endotracheal tube can potentially be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio 1 Granules for Filling ¿ 1 mm (2 cm¿) Recalled by SCIENCE & BIO...
The Issue: Vials of implant bone granules may contain less product then specified on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US...
The Issue: Incorrect labeling in which the front red pouch label did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KliniTray Platte Faxitron Recalled by Klinika Mdical Gmb Due to Potential...
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KliniTray. KlinioTray. Tissue resection margin examination board/small....
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSPIRA AIR BALLOON DILATION SYSTEM 10x40 Recalled by Integra LifeSciences...
The Issue: Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...
The Issue: Preset treatment parameters are not consistently being used in accordance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.