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. 1,061 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,061 in last 12 months

Showing 15321–15340 of 51,202 recalls

Medical DeviceJuly 29, 2021· Lymol Medical Corporation

Recalled Item: LYMOL Medical Elite X Class Rigid Bronchoscope System Recalled by Lymol...

The Issue: Reprocessing instructions were revised November 15, 2020, to new processes...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...

The Issue: There was no label on the pad packaging or notification in the user manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity-i Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Beckman Coulter Inc.

Recalled Item: Power Processor 3K Recalled by Beckman Coulter Inc. Due to Missing splash...

The Issue: Missing splash guard which may expose users to hazardous materials. .

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Liner ECIMA Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Dual Mobility Recalled by Corin Ltd Due to The packaging...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Screw Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee CS Insert Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin BIOLOX Delta Mod Head Recalled by Corin Ltd Due to The packaging...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin MetaFix Hip Stem Recalled by Corin Ltd Due to The packaging system on...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin TriFit TS Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

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

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

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

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

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

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

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

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee Augments Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee Patella Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: Status COVID-19/Flu Rapid Immunoassay for Direct Detection and Differential...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: FaStep COVID-19 IgG/IgM Rapid Test Device Qualitative detection and...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing