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 3106131080 of 51,202 recalls

Medical DeviceMarch 15, 2017· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Ultimax Digital Fluoroscopic X-Ray System...

The Issue: The issue was identified as a firmware problem with the generator.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App versions 2.0.0 Recalled by Roche...

The Issue: A program error (bug) in the Bolus Advisor feature, which could result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2017· Hans Pausch Rontgengeratebau Gmbh

Recalled Item: Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040...

The Issue: During patient interventions with the urology table the radiation is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Valeant Pharmacueticals International

Recalled Item: Small Particle Aerosol Generator Model SPAG-2 6000 Series (SPAG-2). The...

The Issue: SPAG-2 unit nebulizers from Lot J0571670RA were tested at Next Breath for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Nihon Kohden America Inc

Recalled Item: Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The...

The Issue: The Pause function on central monitors will not automatically resume when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Measurement Specialties Inc

Recalled Item: Measurement Specialties Reusable Temperature Probe Autoclavable. Sold as...

The Issue: The reusable temperature probes are provided with instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Accelerate Diagnostics Inc

Recalled Item: Accelerate Pheno system Recalled by Accelerate Diagnostics Inc Due to Rare...

The Issue: Rare isolates of Enterobacteriaceae may generate a susceptible meropenem...

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

Class II — Potential Health HazardOngoing
DrugMarch 13, 2017· Akorn Inc

Recalled Item: Sulfamethoxazole and Trimethoprim Oral Suspension Recalled by Akorn Inc Due...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 13, 2017· Advanced Fresh Concepts Corp

Recalled Item: AFC Edamame Soybeans in Pods Recalled by Advanced Fresh Concepts Corp Due to...

The Issue: Product may be contaminated with listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 12, 2017· Meridian Medical Technologies a Pfizer Company

Recalled Item: EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg Recalled by Meridian...

The Issue: Defective Delivery System; reports of the device failing to activate which...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 12, 2017· Meridian Medical Technologies a Pfizer Company

Recalled Item: EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg Recalled by Meridian...

The Issue: Defective Delivery System; reports of the device failing to activate which...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Fluconazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Claris Lifesciences Inc...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Metronidazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 10, 2017· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is...

The Issue: Product shipped proximate to or past the expiration date listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2017· Heartware

Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...

The Issue: In April 2015, HeartWare, now a part of Medtronic, notified users of a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 9, 2017· Cincinnati Sub-Zero Products Inc

Recalled Item: Hemotherm CE Recalled by Cincinnati Sub-Zero Products Inc Due to Improperly...

The Issue: Improperly rated fuses were used in the manufacture of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· C.R. Bard, Inc.

Recalled Item: SURESTEP Tray Recalled by C.R. Bard, Inc. Due to Misbranded: Product...

The Issue: Misbranded: Product labeled, Not made with natural rubber latex, may in...

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

Class II — Potential Health HazardOngoing