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 2858128600 of 51,202 recalls

DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Toothette Oral Care Suction Swabs with Perox-A-Mint solution. Contains 2...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Toothette Oral Care Suction Toothbrushes with Perox-A-Mint solution....

The Issue: Cross Contamination With Other Products: Oral care solutions were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q CARE q2 Oral Cleansing & Suctioning System Recalled by Sage Products Inc...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q CARE q4 Oral Cleaning & Suctioning System Contains 1 Recalled by Sage...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Wockhardt Usa Inc.

Recalled Item: Enalapril Maleate tablets Recalled by Wockhardt Usa Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: 5mg strength being recalled...

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

Class III — Low RiskOngoing
Refund
DrugAugust 22, 2017· Pfizer Inc.

Recalled Item: HYDROmorphone HCl Injection Recalled by Pfizer Inc. Due to Lack of sterility...

The Issue: Lack of sterility assurance: resulting from use of a damaged sterilizing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Pfizer Inc.

Recalled Item: Levophed (norepinephrine bitartrate) injection Recalled by Pfizer Inc. Due...

The Issue: Lack of sterility assurance: resulting from use of a damaged sterilizing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Centurion Labs, LLC

Recalled Item: Ninjacof-A (Acetaminophen 160 mg Recalled by Centurion Labs, LLC Due to...

The Issue: Microbial contamination of Non-sterile Products; potential B. cepacia...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Centurion Labs, LLC

Recalled Item: Ninjacof (Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Recalled...

The Issue: Microbial contamination of Non-sterile Products; potential B. cepacia...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 22, 2017· Siemens Medical Solutions USA, INC

Recalled Item: Artis oneFloor-mounted system for uncompromised imaging Recalled by Siemens...

The Issue: The possibility exists for the monitor display of Artis one systems with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...

The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...

The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...

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

Class II — Potential Health HazardOngoing
FoodAugust 21, 2017· SUNOPTA GRAINS AND FOODS

Recalled Item: Organic Great Value Dark Sweet Cherry Products Pitted Recalled by SUNOPTA...

The Issue: Testing revealed the presence of Listeria monocytogenes in a finished...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 21, 2017· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...

The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...

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

Class II — Potential Health HazardOngoing
DrugAugust 18, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Paroxetine tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign tablets/capsules: risperidone Tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 18, 2017· Integra LifeSciences Corp.

Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...

The Issue: A quarantined lot of the devices was released for sale. Devices from this...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Olympus Corporation of the Americas

Recalled Item: A20975A "Working insert Recalled by Olympus Corporation of the Americas Due...

The Issue: Olympus has received complaints about fragments of adhesive which detached...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Picture Archiving and Communication System (PACS) with software...

The Issue: Software update to correct several issues that include (1)Potential data...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Invivo Corporation

Recalled Item: Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive...

The Issue: Intermittent communication between the host system and the FlexCardio

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Philips Electronics North America Corporation

Recalled Item: Azurion 3 M12 Recalled by Philips Electronics North America Corporation Due...

The Issue: When using the downscale option with the Allura R9 system or Azurion R1.1...

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

Class II — Potential Health HazardOngoing