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. 981 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
981 in last 12 months

Showing 31321–31340 of 51,202 recalls

DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Cardioplegic Solution Maintenance all strengths Recalled by Advanced Pharma...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Potassium Phosphate all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Dexmedetomidine HCl all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Sodium Citrate all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Penicillin G Potassium all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Ephedrine Sulfate all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 21, 2017· Give and Go Prepared Foods Corp - Finch

Recalled Item: Two-Bite Turtle Brownie Party Platter 16 x 12.2 oz (346g) item number 09904...

The Issue: Dried weevil larvae may be present in the recalled products.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 21, 2017· Give and Go Prepared Foods Corp - Finch

Recalled Item: Two-Bite Pecan Tart 9.2 oz (261g) item number 02023 Recalled by Give and Go...

The Issue: Dried weevil larvae may be present in the recalled products.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 21, 2017· Give and Go Prepared Foods Corp - Finch

Recalled Item: The Bakery Mini Pecan Tarts Part Platter NET WT 16x Recalled by Give and Go...

The Issue: Dried weevil larvae may be present in the recalled products.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 21, 2017· Give and Go Prepared Foods Corp - Finch

Recalled Item: Two-Bite Pecan Tarts Party Platter 16 x 16.2 (460g) item number 09877...

The Issue: Dried weevil larvae may be present in the recalled products.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 21, 2017· Simply Delicious, Inc. dba Bobo's Oat Bars

Recalled Item: Bobo's Coconut Oat Bar 3oz. Packaged in overwrap film per single bar...

The Issue: Bobo's recalled Coconut 3oz Bar due to mold.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint TrueV - 4R Recalled by Siemens Medical Solutions USA...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Recalled...

The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software updates

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· CareFusion 303, Inc.

Recalled Item: MaxGuard Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the MaxGuard Extension Set due to reports of leaks...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Pads Recalled by Terumo...

The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.

Recalled Item: AMS-636 Recalled by Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc....

The Issue: Incorrect priming volume printed on the device package.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint - 3R Recalled by Siemens Medical Solutions USA Inc....

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing