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. 2,438 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,438 in last 12 months

Showing 3486134880 of 49,744 recalls

Medical DeviceDecember 22, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: EVOLIS Microplate System Recalled by Bio-Rad Laboratories, Inc. Due to The...

The Issue: The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Draeger Medical, Inc.

Recalled Item: Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number:...

The Issue: Drager became aware of situations where the error message "Poti unplugged"...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2015· Draeger Medical, Inc.

Recalled Item: Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus...

The Issue: Drager became aware of situations where the error message "Poti unplugged"...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2015· Cook Medical Incorporated

Recalled Item: Zilver¿ 518RX Vascular Stent with Rapid Exchange Delivery System Recalled by...

The Issue: Manufacturing of the joint between the inner catheter and stylet of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Ultradent Products, Inc.

Recalled Item: InterGuard 5.5mm Econo Recalled by Ultradent Products, Inc. Due to Ultradent...

The Issue: Ultradent is recalling InterGuard 5.5mm Econo , lot#s BC2GN and BC4L7...

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

Class II — Potential Health HazardOngoing
DrugDecember 21, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Teva North America

Recalled Item: Capecitabine tablets USP 500 mg Recalled by Teva North America Due to Failed...

The Issue: Failed Dissolution Specifications: low test results at the 18 month time-point

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Chocolate Marshmallows Recalled by Zingerman's Candy Manufactory Due to...

The Issue: Product recalled due to undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Zzang! Original Candy Bar Recalled by Zingerman's Candy Manufactory Due to...

The Issue: Product recalled due to undeclared soy and milk (butter declared).

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Zzang! Wowza Candy Bar Recalled by Zingerman's Candy Manufactory Due to...

The Issue: Product recalled due to undeclared soy; and undeclared milk (cream declared).

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Zzang! Cashew Cow Candy Bar Recalled by Zingerman's Candy Manufactory Due to...

The Issue: Product recalled due to undeclared sub-ingredient soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Zzang! Holiday 4 pack Candy Bars Recalled by Zingerman's Candy Manufactory...

The Issue: Product recalled due to undeclared soy; and undeclared allergen milk (cream...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 21, 2015· ConMed Corporation

Recalled Item: Hip Preservation System Signature Series PreBent Burs under the following...

The Issue: Metal shavings released from burs during use are due to contact between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: The Concerto Basic Shower Trolley is intended for assisted hygiene care...

The Issue: Reports of the bolts connecting the stretcher to the hydraulic piston and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Northeast Laboratory Services, Inc.

Recalled Item: NEL- GBS Medium (Broth 3 ml Fill 13 x 100 mm Screw Cap Tube Catalog No.:...

The Issue: Product marketed without a 510 (k)

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Northeast Laboratory Services, Inc.

Recalled Item: NEL GBS Medium 20 ml in 100x15mm plate (Standard Petri Dish) Catalog No.:...

The Issue: Product marketed without a 510 (k)

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Therakos Inc

Recalled Item: The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog...

The Issue: The Mallinckrodt (Therakos) post-market monitoring process detected an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing