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. 2,591 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,591 in last 12 months

Showing 1732117340 of 29,201 recalls

Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 20705 SMALL PATIENT 1/4 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 25501 3/8" Better Bladder Pack Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 9410 Lurie Chldns Small 1/4 Recalled by Datascope Corporation Due to...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 41201 ECC 3/8 PUMP PAC Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2017· Teleflex Medical

Recalled Item: Teleflex(R) Percuvance(TM) Percutaneous Surgical System Recalled by Teleflex...

The Issue: Teleflex is recalling these products because the jaws of the tool tip may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Central Venous Catheterization Kit with Blue FlexTip Catheter Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Siemens Healthcare Diagnostics

Recalled Item: BC Thrombin Reagent Kit Lot Number 46751 Recalled by Siemens Healthcare...

The Issue: The BC Thrombin Reagent kit lot 46751 (contains Thrombin Reagent lot 517468)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Arrow Multi Lumen CVC Kit (Central venous catheter) Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter) Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: AGB+ Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2017· Fukuda Denshi Co., Ltd.

Recalled Item: Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage:...

The Issue: For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003%...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2017· C.R. Bard, Inc.

Recalled Item: Medivance ArcticGel Small Pad Kit - a box containing a single foil pouch...

The Issue: Hydrogel peeling from the pads.

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

Class II — Potential Health HazardOngoing