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 2742127440 of 51,202 recalls

FoodFebruary 5, 2018· eBars

Recalled Item: RUN ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ Recalled by eBars Due to...

The Issue: The product test positive for peanut allergen which is not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2018· eBars

Recalled Item: GOLF ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ Recalled by eBars Due...

The Issue: The product test positive for peanut allergen which is not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2018· eBars

Recalled Item: TRIM ORGANIC CHOCOLATE ALMOND bar NET WT. 1.6 OZ (45g) Recalled by eBars Due...

The Issue: The product test positive for peanut allergen which is not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2018· eBars

Recalled Item: TRIM ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.8 OZ Recalled by eBars Due...

The Issue: The product test positive for peanut allergen which is not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2018· eBars

Recalled Item: HEAL ORGANIC CHOCOLATE PEANUT bar NET WT. 1.6 OZ (45g) Recalled by eBars Due...

The Issue: The product test positive for almond allergen which is not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx. 0.57 ml Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 14 cm (5.5") Appx 0.27 ml Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 7" Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear Recalled by ICU...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Signature Orthopedics Pty Limited

Recalled Item: Signature Ceramic Femoral Head. Model Number: 111-152-621. The Signature...

The Issue: This recall has been identified due to the batch being mislabeled, with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Dako North America Inc.

Recalled Item: PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to Recalled by Dako...

The Issue: To correct the kit's instructions for use as the storage time for gastric...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· 3M Company - Health Care Business

Recalled Item: 3M Surgical Clipper Professional 9681 Recalled by 3M Company - Health Care...

The Issue: Failure to follow proper charging practices can result in lithium-ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Merit Medical Systems, Inc.

Recalled Item: 1mL Medallion Syringes Are used to inject fluids into Recalled by Merit...

The Issue: Supplier manufacturing defect with the syringe plunger tip.

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2018· ALLERGAN

Recalled Item: NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets Recalled by...

The Issue: Labeling: Not Elsewhere Classified: does not have the required "CII"...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2018· Aurobindo Pharma Ltd.

Recalled Item: Metformin Hydrochloride Tablets Recalled by Aurobindo Pharma Ltd. Due to...

The Issue: Presence of Foreign Tablet: Metformin BP 1000mg was found in bottle of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 100 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans Syringe Fill 360 Recalled by Shippert Medical Technologies Due...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 1000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing