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. 2,372 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,372 in last 12 months

Showing 4456144580 of 49,744 recalls

DrugAugust 29, 2013· Hospira Inc.

Recalled Item: 5% Lidocaine HCl and 7.5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter; report of visible particulates in the glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU (TM) IBUPROFEN Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Labeling: Incorrect or missing lot and/or exp date- This product is being...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Procter & Gamble Co

Recalled Item: Vicks NyQuil Cold and Flu Nighttime Relief Recalled by Procter & Gamble Co...

The Issue: Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2013· Vital Diagnostics, Inc.

Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...

The Issue: High positive calcium bias on plasma sample versus results on serum

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Vital Diagnostics, Inc.

Recalled Item: Vital Diagnostics Envoy Calcium Reagent For In-Vitro Diagnostic Use. PN...

The Issue: High positive calcium bias on plasma sample versus results on serum

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...

The Issue: It was discovered that Carestream received a report from a customer that 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Integra LifeSciences Corp.

Recalled Item: Composite Series Skull Clamp Recalled by Integra LifeSciences Corp. Due to...

The Issue: An investigation of an adverse trend of complaints for the Skull Clamp index...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis Recalled...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek FMS Intermediary Tubing with One-Way valve Product Code:...

The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649...

The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: CARESTREAM DRX -Mobile Retrofit Kit Recalled by Carestream Health Inc. Due...

The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...

The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to The...

The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...

The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Steris Corporation

Recalled Item: Reliance Endoscope Processing System (REPS) Recalled by Steris Corporation...

The Issue: The air pipe that delivers unfiltered ambient air from the procedure room...

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

Class II — Potential Health HazardOngoing
FoodAugust 28, 2013· Premier Foods, LLC

Recalled Item: Tagine Sauce Recalled by Premier Foods, LLC Due to Undeclared Milk

The Issue: Premier Foods is recalling Williams-Sonoma flavored sauces due to undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 28, 2013· Premier Foods, LLC

Recalled Item: Artichoke Pecorino Sauce Recalled by Premier Foods, LLC Due to Undeclared Soy

The Issue: Premier Foods is recalling Williams-Sonoma flavored sauces due to undeclared...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2013· Premier Foods, LLC

Recalled Item: Meyer Lemon Braising Base Recalled by Premier Foods, LLC Due to Undeclared Milk

The Issue: Premier Foods is recalling Williams-Sonoma flavored sauces due to undeclared...

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

Class I — Serious Health HazardOngoing
Refund