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. 2,547 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,547 in last 12 months

Showing 2090120920 of 51,202 recalls

FoodOctober 1, 2019· E.A. Sween Co.

Recalled Item: Market Sandwich Everything Bagel with Smoked Ham Recalled by E.A. Sween Co....

The Issue: Various sandwiches have the potential to be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Recalled by...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. X-Port isp M.R.I Implantable Port Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: PowerFlow Implatable Apheresis IV Port with attachable 9.6 F ChronoFl...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 Recalled by...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 3 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosebud Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosie4 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 7 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing