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 2792127940 of 51,202 recalls

DrugNovember 21, 2017· Lupin Pharmaceuticals Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Lupin Pharmaceuticals...

The Issue: Failed Dissolution Specification

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2017· Teva Pharmaceuticals USA

Recalled Item: Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Teva...

The Issue: Labeling: Incorrect Instructions. "TABLETS IN WEEK 4 ARE INACTIVE" printed...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Paroxetine Tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2017· Elekta Limited

Recalled Item: Integrity R1.2 Recalled by Elekta Limited Due to Potential for positional...

The Issue: Potential for positional errors following automatic table movement (ATM).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Invivo Corporation

Recalled Item: Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio...

The Issue: While in Full Disclosure playback, a user may inadvertently close the Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Elekta Limited

Recalled Item: Agility with Integrity R3.2 Recalled by Elekta Limited Due to Potential for...

The Issue: Potential for positional errors following automatic table movement (ATM).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to When calculating...

The Issue: When calculating electron Monte Carlo dose with a very large number of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2017· Edan Diagnostics

Recalled Item: EDAN Telemetry Transmitter Recalled by Edan Diagnostics Due to Firm became...

The Issue: Firm became aware that it distributed 7 units in the U.S. that included a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2017· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to The syringe...

The Issue: The syringe plunger grippers may fail to automatically close around the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2017· CareFusion 303, Inc.

Recalled Item: Alaris PCA Pump Recalled by CareFusion 303, Inc. Due to The syringe plunger...

The Issue: The syringe plunger grippers may fail to automatically close around the...

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

Class II — Potential Health HazardOngoing
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Liothyronine SR (T3) 20 mcg Capsule Recalled by KRS Global Biotechnology,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 6 Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Benzocaine 20% Recalled by KRS Global Biotechnology, Inc Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: QUADMIX #16 Recalled by KRS Global Biotechnology, Inc Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Sincalide 5 mcg Lyophilized Vials Recalled by KRS Global Biotechnology, Inc...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Amphotericin 60 mg/Chloramphenicol 600 mg/Hydrocortisone 10 mg Otic Powder...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 11 Recalled by KRS Global Biotechnology, Inc...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Vitamin 10 B Lyophilized Vial Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: 7-Keto DHEA 25mg Capsule Recalled by KRS Global Biotechnology, Inc Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Sermorelin Recalled by KRS Global Biotechnology, Inc Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund