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. 2,033 recalls have been distributed to Louisiana in the last 12 months.
Showing 6741–6760 of 29,201 recalls
Recalled Item: Philips DigitalDiagnost C50 -intended for use in generating radiographic...
The Issue: If the PM for the telescopic carriage is not performed annually as defined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQURE Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 Recalled by Radiometer...
The Issue: Due to potential software issue that may result in patient mix-up information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems Recalled by...
The Issue: Due to manufacturing issue, Gastrointestinal (GI) Panel may result in false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray...
The Issue: Issue related to the operation of the arm latch within the column that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual....
The Issue: Error in the Introduction section of the user manual that indicates the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Recalled by Maquet Cardiovascular, LLC Due to Some batches...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 R1.1 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CirClamp with 1.3cm Bell & Insert Reprocessed Recalled by MEDLINE...
The Issue: The CirClamp subassembly found in the kit was the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for Recalled...
The Issue: Not programmed in accordance with specification. The programming affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeLight Fiber Optic Cable: Clear Recalled by Stryker Corporation Due to...
The Issue: Fiber optic cables assembled with not enough epoxy on the proximal end,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Step Bladeless Trocars Recalled by Covidien, LP Due to Medtronic was made...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300 Portable Electric Ventilator Recalled by Philips Respironics,...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Portable Electric Ventilator Recalled by Philips...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...
The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.