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. 2,523 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,523 in last 12 months

Showing 2244122460 of 29,201 recalls

Medical DeviceJuly 31, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: Siemens Symbia T Series Recalled by Siemens Medical Solutions USA, Inc. Due...

The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: Siemens Symbia S Series system Recalled by Siemens Medical Solutions USA,...

The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: Siemens Intevo Series system Recalled by Siemens Medical Solutions USA, Inc....

The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2015· Arrow International Inc

Recalled Item: PICC Kits with Peel-Away Sheath Component Recalled by Arrow International...

The Issue: the catheter peel-away component hub tabs may prematurely detach. One injury...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2015· Arrow International Inc

Recalled Item: Arrow International Recalled by Arrow International Inc Due to saline...

The Issue: saline leakage from unsecured connections between the Touhy Borst adaptor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2015· Beckman Coulter Inc.

Recalled Item: AU5800 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman coulter has received complaints regarding leaking and cracked C...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2015· Beckman Coulter Inc.

Recalled Item: AU680 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman coulter has received complaints regarding leaking and cracked C...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2015· Beckman Coulter Inc.

Recalled Item: AU480 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman coulter has received complaints regarding leaking and cracked C...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Wet Pak* Closed Suction System for Pediatrics Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Synthes (USA) Products LLC

Recalled Item: VEPTR Vertical Expandable Prosthetic Titanium Rib Recalled by Synthes (USA)...

The Issue: The last hole on certain VEPTR Inferior Cradles may be partially formed....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing