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. 2,547 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,547 in last 12 months

Showing 2210122120 of 51,202 recalls

DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets 50 mg 1000 Tablets Recalled by Macleods Pharma...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Macleods...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Macleods...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium andHydrochlorothiazide Tablets 100 mg/25 mg 90 tablets...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2019· Tropical Nut & Fruit Company

Recalled Item: Truly Good Foods Edamame Beans Roasted and Salted 7 oz. Recalled by Tropical...

The Issue: Allergen statement not printed on label of roasted and salted Edamame

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2019· Perrigo Company PLC

Recalled Item: Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron...

The Issue: Product may contain metal fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 20, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Norm-O-Temp model 111Z Recalled by Cincinnati Sub-Zero Products LLC, a...

The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Norm-O-Temp model 111W Recalled by Cincinnati Sub-Zero Products LLC, a...

The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: TURBO DROPS (PHEN 10% / CYCLO 1%/ TROP 1%/ KETO 0.5%) OPHTH SOLN Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: HYDROXOCOBALAMIN 1000 MCG/ML (MDV) Recalled by RXQ Compounding LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: KETAMINE 10 MG/ML INJ SOL SYR (C-III) Recalled by RXQ Compounding LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: TURBO CAINE 2.5 (PHEN2.5/CYCLO1/ TROP1/TETRA 0.5) Recalled by RXQ...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: GLUTATHIONE 200MG/ML (MDV) INJECTION SOLN Recalled by RXQ Compounding LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund