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. 2,506 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,506 in last 12 months

Showing 2704127060 of 29,201 recalls

Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight2 Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort Recalled by...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is...

The Issue: Siemens has confirmed that the TACR method may demonstrate reduced on-board...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******XMax Handpiece***Rx Only***Manufacturer: The Anspach Effort Recalled...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Instratek, Incorporated

Recalled Item: Mini Cannulated Titanium Headed and Headless Screw Set and 2.5 Recalled by...

The Issue: Faded and wrong markings on bone screw Countersink/Depth Gauge instruments...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer:...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******microMax Handpiece***Rx Only***Manufacturer: The Anspach Effort...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2013· Embla System Llc

Recalled Item: embla Embletta Gold (It functions as a Polysomnography Recorder and Recalled...

The Issue: Calibration error for Embla Embletta Gold units calibrated through service...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2013· Cordis Corporation

Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...

The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Fisher & Paykel Healthcare ICON CPAP (continuous positive airway pressure)....

The Issue: Fisher and Paykel Healthcare is recalling the ICON CPAP units because there...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Advanced Sterilization Products

Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24...

The Issue: Advanced Sterilization Products is recalling certain lots of STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Carefusion 2200 Inc

Recalled Item: 1) Adult Manual Resuscitator Recalled by Carefusion 2200 Inc Due to...

The Issue: CareFusion has received four (4) customer reports of a component (oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: HB1C Flex(R) Reagent Cartridge (DF105A Recalled by Siemens Healthcare...

The Issue: Positive bias on the lots listed compared to alternate methods and a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: HbA1c Flex(R) reagent cartridge (K3105A Recalled by Siemens Healthcare...

The Issue: Positive bias on the lots listed compared to alternate methods and a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Brainlab AG

Recalled Item: Brainlab Cranial Navigation System: An Image Guided Surgery System /...

The Issue: Software Error: The effect of setup on overall navigation accuracy could...

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

Class I — Serious Health HazardOngoing