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. 2,547 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,547 in last 12 months

Showing 1896118980 of 29,201 recalls

Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 20x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 15mmdx46cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 15mmdx48cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 15x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Zimmer Biomet, Inc.

Recalled Item: MEDTECH ROSA Brain 3.0 The device is intended for the Recalled by Zimmer...

The Issue: Unapproved change made by the supplier.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee and Zeego fluoroscopic x-ray system Recalled by Siemens Medical...

The Issue: A gap in the housing of the wireless foot switch could potentially result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Zimmer Biomet, Inc.

Recalled Item: MEDTECH ROSA Spine 1.0.2 The device is intended for the Recalled by Zimmer...

The Issue: Unapproved change made by the supplier.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q and Q.Zen fluoroscopic x-ray system Recalled by Siemens Medical...

The Issue: A gap in the housing of the wireless foot switch could potentially result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Welch Allyn Inc

Recalled Item: Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400 Recalled by Welch...

The Issue: A defective electrical component in the battery charging circuit in two lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Artis fluoroscopic x-ray system Recalled by Siemens Medical Solutions...

The Issue: A gap in the housing of the wireless foot switch could potentially result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT model number 882480 BrightView and BrightView X are...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT model number 882482 BrightView and BrightView X are Recalled...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X 3/4 model number 882479 BrightView and BrightView X Recalled by...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips North America, LLC

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...

The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X 3/8 model number 882478 BrightView and BrightView X Recalled by...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 23, 2017· Hill-Rom, Inc.

Recalled Item: TotalCare Bed Systems Recalled by Hill-Rom, Inc. Due to The bed exit alarm...

The Issue: The bed exit alarm may not function properly if the alarm has been armed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Oncology CT - 728243 Computed Tomography X-ray systems...

The Issue: When the user performs a retrospective respiratory gated 4D CT scan with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Streck

Recalled Item: Cyto-Chex BCT - blood specimen collection device - Immunophenotyping...

The Issue: Complaints of the 2.0ml tube stopper coming loose during phlebotomy when...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Enzyme 2 Calibrator Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has confirmed a positive bias of up to 41% in...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 23, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Radiology CT - 728244 Computed Tomography X-ray systems...

The Issue: Philips identified a 4D CT pulmonary phase issue on Brilliance BigBore...

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

Class II — Potential Health HazardOngoing