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. 2,506 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,506 in last 12 months

Showing 2976129780 of 51,202 recalls

DrugMay 24, 2017· Shionogi Inc.

Recalled Item: Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...

The Issue: Presence of foreign substance: The recall was initiated due to black...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodMay 24, 2017· Woodland Foods

Recalled Item: D'Allesandro Woodland Foods De-stemmed Birdseye Chiles 1 Recalled by...

The Issue: Trace amounts of undeclared peanut found in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 24, 2017· NeuroLogica Corporation

Recalled Item: Samsung GU60A system- Digital X-ray Imaging Systems are intended for...

The Issue: When performing the Stitching function on GU60A system, unintended area is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2017· Merge Healthcare, Inc.

Recalled Item: Merge OrthoPACS software. The firm name on the label is Merge Healthcare...

The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2017· Merge Healthcare, Inc.

Recalled Item: Merge OrthoPACS software. Recalled by Merge Healthcare, Inc. Due to A...

The Issue: A migrated study that has annotations will display the annotations, but when...

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

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

Recalled Item: Dimension Vista Protein 1 Control H Recalled by Siemens Healthcare...

The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage:...

The Issue: Underestimates the lead concentration of venous blood samples when the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number:...

The Issue: Cracks may occur over time on the tube holding shaft near the base of the...

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

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

Recalled Item: Dimension Vista Protein 1 Calibrator Recalled by Siemens Healthcare...

The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Pentax of America Inc

Recalled Item: Ultrasound Video Gastroscope Recalled by Pentax of America Inc Due to Error...

The Issue: Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU FDR Visionary Catalog Number: FDR Visionary Suite Stationary x-ray...

The Issue: Cracks may occur over time on the tube holding shaft near the base of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Pentax of America Inc

Recalled Item: Ultrasound Video Gastroscope Recalled by Pentax of America Inc Due to Error...

The Issue: Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used...

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

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

Recalled Item: Dimension Vista Protein 1 Control Recalled by Siemens Healthcare...

The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...

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

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

Recalled Item: Dimension Vista Protein 1 Control M Recalled by Siemens Healthcare...

The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU RADspeed Pro Catalog Number: RADspeed Pro Recalled by Shimadzu...

The Issue: Cracks may occur over time on the tube holding shaft near the base of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra and LeadCare Plus test Kits. Product...

The Issue: Underestimates the lead concentration of venous blood samples when the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Quick-Connect Drill 3.5 mm Diameter 11 cm...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Becton Dickinson & Co.

Recalled Item: TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...

The Issue: Listeria monocytogenes contamination of non-sterile plated media

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Calibrated Drill Long 4.3mm Recalled by Zimmer...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing