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. 2,690 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,690 in last 12 months

Showing 56415660 of 29,201 recalls

Medical DeviceSeptember 1, 2023· Onkos Surgical, Inc.

Recalled Item: Male-Female Midsection with the following sizes and model numbers. a....

The Issue: Potential for breach of Tyvek seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Onkos Surgical, Inc.

Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...

The Issue: Potential for breach of Tyvek seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Angel Medical Systems, Inc.

Recalled Item: Brand Name: The Guardian System Product Name: The Guardian Model/Catalog...

The Issue: Device reaching End of Service prematurely.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Convergent Dental

Recalled Item: Solea Models 2.0 and 3.0 Laser Surgical Instrument Recalled by Convergent...

The Issue: It has been found that potential unintended laser activation can occur...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: LAVH Recalled by American Contract Systems, Inc. Due to During an internal...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Robotics Pack SAH Recalled by American Contract Systems, Inc. Due to During...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Robotics Pack Recalled by American Contract Systems, Inc. Due to During an...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Vasc. Open CVOR SJH Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: CVS PCSU SJH Recalled by American Contract Systems, Inc. Due to During an...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Pediatric Heart SJH Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Cath Cardiac Pack Recalled by American Contract Systems, Inc. Due to During...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Sub Q Recorder Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Robotics Pack Recalled by American Contract Systems, Inc. Due to During an...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Breast Plastics Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Pediatric Urology Wolson Pack Recalled by American Contract Systems, Inc....

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: General Pack Recalled by American Contract Systems, Inc. Due to During an...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: (1) Over-ear headphones used with the MAGNETOM Amira MAGNETOM Free.Star...

The Issue: In some cases, when lubricating grease is present within the headband of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Recalled by Access Vascular, Inc Due to Specific...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Maximal Barrier Kit Recalled by Access Vascular,...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vitals Monitor Recalled by Philips North America Llc Due to A...

The Issue: A software issue prevents the monitor from alarming when the high/low...

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

Class II — Potential Health HazardOngoing