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. 1,807 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,807 in last 12 months

Showing 3372133740 of 51,202 recalls

Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: S7 MACH FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Cranial S7. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Fusion ENT Application. The software application is sent in CD Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Spine. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH AxiEM Cranial Treon. The software application is sent in Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH Cranial Treon. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
FoodJuly 16, 2016· ConAgra Frozen Foods, Inc

Recalled Item: PF Chang's Home Menu Brand Shrimp Lo Mein Recalled by ConAgra Frozen Foods,...

The Issue: Metal fragments were discovered in an raw ingredient used in the manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2016· The Harvard Drug Group

Recalled Item: Diocto Liquid (docusate sodium) 50 mg/5 mL Stool Softener Laxative Recalled...

The Issue: Microbial contamination of Non-Sterile Products; positive findings of...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 15, 2016· Teva North America

Recalled Item: Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol Recalled...

The Issue: Failed Content Uniformity Specifications: out of specification test result...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Roche/Hitachi MODULAR Analytics Combination Systems Modular D/P: Clinical...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 471 centrifuge unit calculator/data processing module Recalled by...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 701 Post-Analytical Unit calculator/data processing module Recalled...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: VS II Aliquoter System calculator/data processing module Recalled by Roche...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: URISYS 2400 Urine Analyzer Automated Urinalysis System Product Usage: The...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: RSD 800 Sorting System calculator/data processing module Recalled by Roche...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 501 Post-Analytical Unit calculator/data processing module Recalled...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 512 Pre-Analytical Instrument calculator/data processing module...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 612 Pre-Analytical Instrument calculator/data processing module...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: RSD 800A Aliquoting System calculator/data processing module Recalled by...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing