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. 2,653 recalls have been distributed to Louisiana in the last 12 months.
Showing 11101–11120 of 51,202 recalls
Recalled Item: regard MAJOR CRANI Recalled by ROi CPS LLC Due to Surgical convenience kits...
The Issue: Surgical convenience kits were distributed containing 3M surgical drapes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ¿regard EYE TRAY Recalled by ROi CPS LLC Due to Surgical convenience kits...
The Issue: Surgical convenience kits were distributed containing 3M surgical drapes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: regard SPINE PACK Recalled by ROi CPS LLC Due to Surgical convenience kits...
The Issue: Surgical convenience kits were distributed containing 3M surgical drapes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ¿regard SHOULDER PK Recalled by ROi CPS LLC Due to Surgical convenience kits...
The Issue: Surgical convenience kits were distributed containing 3M surgical drapes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO-fit Neonatal Endotracheal Tube Grip Recalled by CooperSurgical, Inc. Due...
The Issue: Firm has received 11 complaints involving a loose or detached metal clips,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Susvimo (ranibizumab injection) Recalled by Genentech Inc Due to Defective...
The Issue: Defective Delivery System: Commercial implants do not meet the filed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg Recalled by SUN...
The Issue: Presence of Foreign Substance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GFUEL brand Watermelon Limeade Energy Drink Recalled by G FUEL LLC Due to...
The Issue: Product label does not declare the correct amount of caffeine.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000...
The Issue: Warehouse experienced temperature excursions in July and August 2021. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Progressa Bed System Recalled by Baxter Healthcare Corporation Due...
The Issue: The compression links on impacted Progressa beds, listed in Appendix A, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...
The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...
The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18239: ASM Omnipod Dash PDM Recalled by Insulet Corporation Due to The firm...
The Issue: The firm has become aware of PDM battery issues, including battery swelling,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to...
The Issue: Two electronic diode components (D1 & D4) placed in the reverse orientation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extension Tabletop for Operating Table System 1140 Recalled by Getinge Usa...
The Issue: The back rest may unintentionally drop suddenly, resulting in adverse health...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER...
The Issue: Due to a defect in the outer pouch sterile seal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GentleWave System APM Procedure Instrument with Matrix Recalled by Sonendo...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.