Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,448 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,448 in last 12 months

Showing 3124131260 of 49,744 recalls

Medical DeviceOctober 28, 2016· The Binding Site Group, Ltd.

Recalled Item: Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S...

The Issue: A change in the calibration curve causing an increase in false prozone flags.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· Natus Medical Incorporated

Recalled Item: Natus neoBLUE blanket LED Phototherapy system Recalled by Natus Medical...

The Issue: neoBLUE blanket LED Phototherapy System distributed since release of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· Hologic, Inc

Recalled Item: SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices....

The Issue: Breach in sterile barrier compromising product sterility

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

Class II — Potential Health HazardOngoing
FoodOctober 28, 2016· Mondelez International

Recalled Item: Nabisco Oreo Fudge Creme Mint Variety Recalled by Mondelez International Due...

The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 28, 2016· Aldi Inc

Recalled Item: Simply Nature Organic Red Split Lentils Recalled by Aldi Inc Due to...

The Issue: Product may contain undeclared wheat

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2016· Mondelez International

Recalled Item: Nabisco Oreo Fudge Creme Original Variety Recalled by Mondelez International...

The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 28, 2016· Life Rising Corp S

Recalled Item: Life Rising TT Side Head Regulator Recalled by Life Rising Corp S Due to...

The Issue: High levels of lead discovered in product.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 28, 2016· Aldi Inc

Recalled Item: Simply Nature Organic Green Lentils Recalled by Aldi Inc Due to Undeclared Wheat

The Issue: Product may contain undeclared wheat

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Love My Tru Body

Recalled Item: Skinny Bee Diet capsules Recalled by Love My Tru Body Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: presence of undeclared sibutramine,...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol...

The Issue: Failed Stability Specifications: Low Out of Specification results for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 27, 2016· Amerisource Health Services

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets Recalled by Amerisource...

The Issue: Failed Dissolution Specifications: The firm was notified that there was a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADett Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADgic Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: Mucosal Atomization Device (MAD) Recalled by Teleflex Medical Due to Product...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: FLEXI NOZZLE SHORT Product Usage: These products are used for Recalled by...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: FLEXI NOZZLE LONG Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing