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. 2,523 recalls have been distributed to Louisiana in the last 12 months.
Showing 22601–22620 of 29,201 recalls
Recalled Item: Hardy Diagnostics VRE Broth Recalled by Hardy Diagnostics Due to Hardy...
The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics MDR Acinetobacter container type: 15x100mm monoplate...
The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics BEA Agar with Vancomycin container type: 15x100mm...
The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics MacConkey Agar with CiPRP Recalled by Hardy Diagnostics...
The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam Gamma Camera Recalled by Siemens Medical Solutions USA, Inc. Due to...
The Issue: Potential failure mode related to the radial brake, where the detector was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics BEA Agar with VGA container type: 15x100mm monoplate...
The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON S 1000 Recalled by Siemens Medical Solutions USA, Inc. Due to...
The Issue: Potential measurement error on ACUSON S Family ultrasound system when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON S2000 and ACUSON S3000 ultrasound systems with the Virtual Recalled...
The Issue: Potential measurement error on ACUSON S Family ultrasound system. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S2 Fluid Pack on the Cobas b 221 system- Catalog Recalled by Roche...
The Issue: The affected S2 fluid packs may generate a transponder error when the fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical P-440 Portable Ceiling Lift Recalled by ErgoSafe Products, LLC...
The Issue: There is a potential the sling loops may not stay attached to the carry bar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical P-600 Portable Ceiling Lift Recalled by ErgoSafe Products, LLC...
The Issue: There is a potential the sling loops may not stay attached to the carry bar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/L Recalled...
The Issue: The affected part and lot numbers of the TI Matrix Pre-Bent Maxillary Plates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30inch Dual Port/Single Bladder Disposable Tourniquet Cuff with PLC Recalled...
The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18inch Dual Port/Single Bladder Disposable Tourniquet Cuff Recalled by...
The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EKOS EkoSonic Control Unit is intended exclusively for use Recalled by...
The Issue: The Connector Interface Cable (CIC) was not recognized by the EkoSonic PT-3B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-Two Adult Ventilation Timer Recalled by O-Two Medical Technologies, Inc....
The Issue: Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems with software versions...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.