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 3040130420 of 51,202 recalls

Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Z NAIL PF 14MM X 46CM UNIV Z NAIL GT Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSA-FX II STD TUBE 130DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSA-FXII SC TUBE PLT 90DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
DrugApril 28, 2017· PAR Sterile Products LLC

Recalled Item: Buprenorphine HCI Injection Recalled by PAR Sterile Products LLC Due to...

The Issue: Crystallization: due to the presence of white, crystalline particulates,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 27, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol Transdermal System) 0.1 mg per day Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for peel force from the...

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

Class III — Low RiskOngoing
Refund
DrugApril 27, 2017· Hetero USA Inc

Recalled Item: Acyclovir Tablets Recalled by Hetero USA Inc Due to Presence of Foreign...

The Issue: Presence of Foreign Substance: human hair melded into tablet.

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· AbbVie Inc.

Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...

The Issue: PEG kits have the potential for one of the following defects: missing...

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

Class II — Potential Health HazardOngoing