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. 1,827 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,827 in last 12 months

Showing 3080130820 of 51,202 recalls

FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps Sweet Me Creamery Strawberry Rhubarb Cobbler Recalled by Kemps, LLC...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps Sweet Me Creamery Maple Toffee Blondie Recalled by Kemps, LLC Due to...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps YO2 Frozen Yogurt Mudslide Recalled by Kemps, LLC Due to Kemps is...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps Sweet Me Creamery Salted Caramel Brownie Recalled by Kemps, LLC Due to...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps Sweet Me Creamery Expresso Mocha Recalled by Kemps, LLC Due to Kemps...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps YO2 Frozen Yogurt Cold Brewed Coffee Recalled by Kemps, LLC Due to...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps Sweet Me Creamery Chocolate Peanut Butter Pretzel Recalled by Kemps,...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps YO2 Frozen Yogurt Very Vanilla Recalled by Kemps, LLC Due to Kemps is...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps Sweet Me Creamery Creamy Dark Chocolate Mint Recalled by Kemps, LLC...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps YO2 Frozen Yogurt Raspberry Cheesecake Recalled by Kemps, LLC Due to...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 14, 2017· Cardiovascular Systems Inc

Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to Cardiovascular Systems,...

The Issue: Cardiovascular Systems, Inc. (CSI). has initiated a recall to remove 1,396...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2017· Del Mar Reynolds Medical, Ltd.

Recalled Item: Spacelabs Healthcare Arkon Anesthesia Delivery System is intended for use...

The Issue: Reports of the Canister Carrier breaking during absorbent exchange or during...

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

Class II — Potential Health HazardOngoing
DrugApril 13, 2017· Spectrum Laboratory Products, Inc.

Recalled Item: Estradiol (17-B-Estradiol Recalled by Spectrum Laboratory Products, Inc. Due...

The Issue: CGMP Deviations: these repackaged and redistributed products are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2017· Spectrum Laboratory Products, Inc.

Recalled Item: Levonorgestrel Recalled by Spectrum Laboratory Products, Inc. Due to CGMP...

The Issue: CGMP Deviations: these repackaged and redistributed products are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2017· Standard Homeopathic Company

Recalled Item: Hyland's Baby Teething Tablets [Calcarea Phosporica 6X HPUS Recalled by...

The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2017· Standard Homeopathic Company

Recalled Item: Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS...

The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing