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 2606126080 of 51,202 recalls

Medical DeviceJune 29, 2018· Quasar Bio-Tech, Inc.

Recalled Item: Pure Rayz Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not receive...

The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage:...

The Issue: QFix has advised Mevion Medical Systems that they are identifying...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Quasar Bio-Tech, Inc.

Recalled Item: Quasar MD Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...

The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Luminex Corporation

Recalled Item: Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by...

The Issue: An incorrect control board and firmware installed in some of the Hand Held...

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

Class II — Potential Health HazardOngoing
FoodJune 29, 2018· Sisel International Llc

Recalled Item: Sisel Recalled by Sisel International Llc Due to Firm is recalling SiselRipt...

The Issue: Firm is recalling SiselRipt due to the presence of an unapproved artificial...

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

Class III — Low RiskOngoing
Refund
FoodJune 29, 2018· LL'S MAGNETIC CLAY INC

Recalled Item: Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal...

The Issue: The recalled dietary supplement has the potential to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2018· Pinnacle Food Group, Llc

Recalled Item: Wish Bone House Italian Salad Dressing 15 oz. Recalled by Pinnacle Food...

The Issue: The recall was initiated after learning from a retail customer that a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 28, 2018· Datex-Ohmeda, Inc.

Recalled Item: The Neonatal Flow Sensor Cable used on devices CARESCAPE R860 Recalled by...

The Issue: The Neonatal Flow Sensor Cable may be missing the connector housing exposing...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2018· LUPIN SOMERSET

Recalled Item: Nitrofurantoin Oral Suspension USP Recalled by LUPIN SOMERSET Due to...

The Issue: Subpotent Drug and Failed Content Uniformity.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2018· PFIZER

Recalled Item: Daptomycin for Injection Recalled by PFIZER Due to Microbial Contamination...

The Issue: Microbial Contamination of Sterile Products: Product associated with reports...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost R90 (Stitching Patient Support) 709030 Recalled by Philips...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips Medical Systems Gmbh, DMC Due to...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Upgrades (Stitching Patient Support) 712083 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing