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. 2,604 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,604 in last 12 months

Showing 1628116300 of 29,201 recalls

Medical DeviceMay 8, 2018· Stryker Sustainability Solutions

Recalled Item: Reprocessed HARMONIC Ace¿ +7 Recalled by Stryker Sustainability Solutions...

The Issue: Stryker Sustainability Solutions has received an increase in reports...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Human Design Medical Llc

Recalled Item: Vivo 65 Recalled by Human Design Medical Llc Due to Some Vivo 65 devices...

The Issue: Some Vivo 65 devices have an unreleased version of the Firmware upgrade tool.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm has identified two lots of test strips that are out of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm identified four US lots of test strips out of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm has identified two lots of test strips that are out of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Sodium Slides Recalled by Ortho-Clinical Diagnostics Due to Potential...

The Issue: Potential for positively biased results

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Thermo Fisher

Recalled Item: remel SUPERPACK CS/ 500 SEG/FLASK Recalled by Thermo Fisher Due to Product...

The Issue: Product may fail performance testing for S aureus ATCC 43300.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 43 Recalled by Beckman Coulter Inc. Due to...

The Issue: The drug dilution sequence for Moxifloxacin printed on the panel is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Synthes (USA) Products LLC

Recalled Item: Synthes Torque Limiting Handle Recalled by Synthes (USA) Products LLC Due to...

The Issue: The adapter may demonstrate a degradation of function as the final products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Vascular Solutions, Inc.

Recalled Item: Drainer(R) Centesis Catheters: (a) Recalled by Vascular Solutions, Inc. Due...

The Issue: The supplier of Drainer(R) centesis catheters notified Vascular Solutions,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...

The Issue: The devices may have been assembled with an internal component that may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Medtronic Neurosurgery

Recalled Item: Medtronic Clip Gun Magazines are packaged in individually sealed pouches...

The Issue: The packaging sterile barrier does not comply with the applicable packaging...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...

The Issue: Ingress of fluids into the device can affect various electronic circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 3, 2018· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...

The Issue: The devices may have been assembled with an internal component that may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: 1) Drainer Centesis Catheter Recalled by Galt Medical Corporation Due to The...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: Tearaway Introducers Recalled by Galt Medical Corporation Due to The...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...

The Issue: The bottles are mislabeled with an incorrect part number.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N...

The Issue: The diameter of the drill sleeve guide raw material was found to be under...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing