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. 970 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
970 in last 12 months

Showing 37181–37200 of 51,202 recalls

DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: L-Tyrosine Injectable Recalled by Downing Labs, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Magnesium Chloride Hexahydrate Injection 200mg/mL Recalled by Downing Labs,...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Methylcobalamin Buffered Injectable Recalled by Downing Labs, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: L-Glutathione Injection Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: HCG (Lyophilized) Injectable Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: L-Glutamine Injectable Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: L-Arginine Injection Recalled by Downing Labs, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Methylcobalamin Injection Buffered 5mg/mL Recalled by Downing Labs, LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Phosphatidylcholine/Deoxycholic Acid Injection (Preserved) 50 ML 10/4.75%...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 15, 2015· Euro Diagnostica AB

Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...

The Issue: Complaint investigation concluded that although product quality requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Stryker Sustainability Solutions

Recalled Item: SSS Reprocessed Zimmer Recalled by Stryker Sustainability Solutions Due to...

The Issue: It was reported that packaging was not properly sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Teleflex Medical

Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...

The Issue: The defective component can cause gas leakage through the device. This can...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· TZ Medical Inc.

Recalled Item: Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus...

The Issue: The IFU of the Neptune Plus Pads, does not match that submitted in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...

The Issue: The following MRx software issue has been identified: MRx model M3535A with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2015· Event Medical LTD

Recalled Item: Inspiration Ventilator System Recalled by Event Medical LTD Due to A...

The Issue: A component on the systems power board can fail in a manner which can cause...

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

Class I — Serious Health HazardOngoing