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. 2,518 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,518 in last 12 months

Showing 2330123320 of 29,201 recalls

Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 8MM x 14MM Fluted Drum Recalled by The Anspach Effort, Inc. Due to...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 5MM Fluted Ball Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 2.3MM Fluted Matchstick Recalled by The Anspach Effort, Inc. Due...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 4MM x 11 MM Fluted Barrel Recalled by The Anspach Effort, Inc. Due...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Extra Coarse Diamond Ball Recalled by The Anspach Effort, Inc. Due...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Fluted Drum Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Fluted Acorn Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 4MM Diamond Ball Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Fluted Drum Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 5MM Diamond Ball Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Fluted Barrel Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 8MM x 12.5MM Fluted Barrel Recalled by The Anspach Effort, Inc....

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· CooperSurgical, Inc.

Recalled Item: McKesson Medi-Pak Vaginal Speculum Recalled by CooperSurgical, Inc. Due to...

The Issue: Small sized specula were incorrectly packaged in printed bags for the medium...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to Study...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Uroskop Omnia Max Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Axiom Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Philips Ultrasound, Inc.

Recalled Item: EPIQ 7 Ultrasound System with Pediatric Cardiology option Recalled by...

The Issue: When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Alphatec Spine, Inc.

Recalled Item: 4.0mm Variable Angle Recalled by Alphatec Spine, Inc. Due to Mislabeling

The Issue: During a field audit it was discovered by an employee that a 16mm Trestle...

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

Class II — Potential Health HazardOngoing