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. 2,108 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,108 in last 12 months

Showing 69216940 of 51,202 recalls

Medical DeviceJanuary 3, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse CV 6. with AR. A web-based application as the Recalled by FUJIFILM...

The Issue: The LV Mass (2D Bullet) equation may be calculated incorrectly, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T Initial system. Model (REF) Numbers 781178. Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T Conversion. Model (REF) Numbers 781346 Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva XR. Model (REF) Numbers 781153 Recalled by Philips North America Due...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Intera Achieva 1.5T Pulsar. Model (REF) Number 781171. Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 3.0T. Model. (REF) Numbers 781277 Recalled by Philips North America...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Ingenia 1.5T CX. Model (REF) Numbers 781262 Recalled by Philips North...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: SmartPath to dStream for 1.5T. Model (REF) Numbers 781260 Recalled by...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse Cardiology PACS V7.3.0 Recalled by FUJIFILM Healthcare Americas...

The Issue: The LV Mass (2D Bullet) equation may be calculated incorrectly, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Intera 1.5T Achieva Nova. Model (REF) Numbers 781172. Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...

The Issue: A software error caused an increase in tray gripper motion errors that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Framegrabber card may not perform as intended. Monitor may show no...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Framegrabber card may not perform as intended. Monitor may show no...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Disk Bay may not perform as intended. System may stop functioning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Disk Bay may not perform as intended. System may stop functioning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...

The Issue: Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2024· Zimmer Surgical Inc

Recalled Item: 3:1 Dermacarrier Recalled by Zimmer Surgical Inc Due to Due to manufacturing...

The Issue: Due to manufacturing issue, the product is labeled as 3:1 ratio, but the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 2, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tizanidine Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Presence of Foreign tablets/capsules - identified as tizanidine 2 mg tablets.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 30, 2023· Mead Johnson & Company LLC

Recalled Item: Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6...

The Issue: Product has the potential to be contaminated with Cronobacter sakazakii.

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 29, 2023· Ascend Laboratories, LLC

Recalled Item: Ibuprofen and Famotidine Tablets 800mg/26.6mg Recalled by Ascend...

The Issue: Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet...

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

Class II — Potential Health HazardOngoing
Refund