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

51,202 total recalls
925 in last 12 months

Showing 44141–44160 of 51,202 recalls

Medical DeviceMarch 13, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...

The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The products are labeled as sterile but were not sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...

The Issue: The products are labeled as sterile but were not sterilized.

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

Class II — Potential Health HazardOngoing
DrugMarch 13, 2014· Pain Free By Nature

Recalled Item: REUMOFAN PLUS Tablets Recalled by Pain Free By Nature Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 11, 2014· Paddock Laboratories, LLC

Recalled Item: Perrigo Recalled by Paddock Laboratories, LLC Due to Presence of Particulate...

The Issue: Presence of Particulate Matter Perrigo is recalling seven lots of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...

The Issue: The products are being recalled because they did not meet minimum needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Deknatel Teleflex Medical Silk Black Braided Silk Suture Nonabsorbable...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Teleflex Medical Recalled by Teleflex Medical Due to Product does not meet...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Teleflex Medical Recalled by Teleflex Medical Due to Product does not meet...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Nonabsorbable Surgical Suture Recalled by Teleflex Medical Due to Product...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Fixt Suture Bonded Plus Violet Braided Polyglycolic Acid Coated Suture...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Suture Recalled by Teleflex Medical Due to The products are being recalled...

The Issue: The products are being recalled because they did not meet minimum needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port  Standard Length...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 mm Weck¿ Recalled by Teleflex Medical Due to Complaints were received...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...

The Issue: The products are being recalled because they did not meet minimum needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Weck¿ Vista" Recalled by Teleflex Medical Due to Complaints were received of...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Bard Fixt Suture Braided Polyester Recalled by Teleflex Medical Due to...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...

The Issue: The products are being recalled because they did not meet minimum needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Standard Length...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

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

Class II — Potential Health HazardOngoing