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. 1,061 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,061 in last 12 months

Showing 15741–15760 of 51,202 recalls

Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards VAMP Jr. 6 in (15 cm) Recalled by Edwards Lifesciences, LLC Due to...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Owen Mumford USA, Inc.

Recalled Item: Unifine Pentips Plus Recalled by Owen Mumford USA, Inc. Due to Mixed Up. Two...

The Issue: Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (30 cc)/VAMP Jr/52 in (132 cm) Kit Recalled by Edwards...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2021· McKesson Corporation dba McKesson Drug Company

Recalled Item: Levetiracetam Tablets USP Recalled by McKesson Corporation dba McKesson Drug...

The Issue: Labeling; Wrong Barcode; error in the machine-readable barcode which could...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 25, 2021· Medline Industries Inc

Recalled Item: Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Recalled...

The Issue: Potential for mold contamination (Aspergillus vadensis)

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro - Patient physiological monitor Recalled by Remote Diagnostic...

The Issue: The Tempus Pro (Trizeps 7 only) when used in combination with a specified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Galan 3T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· GE Healthcare, LLC

Recalled Item: CARESCAPE PDM-Masimo SpO2. Physiological data monitor. Recalled by GE...

The Issue: Masimo SpO2 Saturation Values can become frozen after an extended length of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Titan 3T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen Recalled by...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Sunstar Americas, Inc.

Recalled Item: SUNSTAR G.U.M PERIOSHIELD Oral Health Rinse Recalled by Sunstar Americas,...

The Issue: Products may be contaminated with micro-organisms Burkholderia cepacia...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC Due...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Toshiba Vantage Tiitan 1.5T with Standard gradient Recalled by Canon Medical...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Tiitan 1.5T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing