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. 1,727 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,727 in last 12 months

Showing 5052150540 of 51,202 recalls

Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HF7P....

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Spacelabs Healthcare, Llc

Recalled Item: The product is Pathfinder SL Recalled by Spacelabs Healthcare, Llc Due to...

The Issue: The firm received reports of the Pathfinder LS software crashing after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
FoodMay 11, 2012· Brinkhoff & Monoson Inc

Recalled Item: Organic Paprika packaged under the following labels: (1) Archer Farms...

The Issue: Organic Paprika contains unapproved colors.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 volume imaging ultrasound systems at software versions VA16C...

The Issue: In some cases, the system is unable to capture a clip or image during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 12-GAUGE...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB CATHETER KIT-DR BARTLES Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS ANTEGRADE: CARDIOPLEGIA CANNULA: ROOT INFUSION VENT/CATHETER WITH 14-...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: XC HEART/LUNG PACK W/SX25RX Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing