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. 2,609 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,609 in last 12 months

Showing 1606116080 of 29,201 recalls

Medical DeviceJune 15, 2018· Shimadzu Medical Systems Usa Com

Recalled Item: TRINIAS Digital Angiographic System intended to be used for cardiac...

The Issue: Due to a software issue the C-arm may unexpectedly moved when being moved to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2018· Maquet SAS

Recalled Item: VOLISTA StandOP Surgical Light Recalled by Maquet SAS Due to Certain VOLISTA...

The Issue: Certain VOLISTA StandOP Surgical Lights have been identified as having a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Smith & Nephew, Inc.

Recalled Item: JOURNEY BCS Knee Conventional Polyethylene Inserts: 74023111 Recalled by...

The Issue: The data in the National Joint Registry of England, Wales and Northern...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Smith & Nephew, Inc.

Recalled Item: Journey BCS Knee CoCr Femoral Components Recalled by Smith & Nephew, Inc....

The Issue: The data in the National Joint Registry of England, Wales and Northern...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Bard Medical Division

Recalled Item: Arctic Sun Temperature Management System Recalled by Bard Medical Division...

The Issue: An improper wiring connection on the chiller assembly may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Beekley Corporation

Recalled Item: TomoSPOT Recalled by Beekley Corporation Due to There is a potential for...

The Issue: There is a potential for imaging artifact to mimic calcifications on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Beekley Corporation

Recalled Item: S-SPOT Recalled by Beekley Corporation Due to There is a potential for...

The Issue: There is a potential for imaging artifact to mimic calcifications on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Smith & Nephew, Inc.

Recalled Item: JOURNEY BCS OXINIUM Knee Femoral Components Recalled by Smith & Nephew, Inc....

The Issue: The data in the National Joint Registry of England, Wales and Northern...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Beekley Corporation

Recalled Item: O-SPOT Recalled by Beekley Corporation Due to There is a potential for...

The Issue: There is a potential for imaging artifact to mimic calcifications on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Leica Microsystems, Inc.

Recalled Item: Leica Biosystems HistoCore SPECTRA ST Recalled by Leica Microsystems, Inc....

The Issue: These devices have an incorrect specification against safety standard...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2018· Inspire Medical Systems Inc.

Recalled Item: Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive...

The Issue: Incorrect use-by date on the device registration/patient file labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2018· Teleflex Medical Europe Ltd

Recalled Item: Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2" Recalled by Teleflex...

The Issue: The incorrect plastic was used to manufacture the handles of these shears,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2018· Philips Respironics, Inc.

Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to In 2018, Philips...

The Issue: In 2018, Philips Respironics added foam replacement to the preventive...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing