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. 2,534 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,534 in last 12 months

Showing 2124121260 of 29,201 recalls

Medical DeviceFebruary 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista Blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: The two sets of wires (4 total wires) exiting from the EMI filters were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Interlocking Bolt Recalled by Synthes (USA) Products LLC Due to...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...

The Issue: Siemens found a defective part in their production line which could increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Biomet, Inc.

Recalled Item: Verso Shoulder Forked Retractor (Comprehensive Instrumentation 2 Prong...

The Issue: Zimmer Biomet Inc. Verso Shoulder Forked Retractor (Comprehensive...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Inspiration with Tomosynthesis functionality Recalled by Siemens...

The Issue: A potential system fatal error may occur during tomosynthesis reconstruction...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Zimmer Spine, Inc.

Recalled Item: Universal Clamp¿ System (IFU : SNA027-N-90001). Provides the stability...

The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...

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

Class II — Potential Health HazardOngoing