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 3224132260 of 49,744 recalls

FoodAugust 8, 2016· Pharmatech LLC

Recalled Item: Cerovite Liquid Recalled by Pharmatech LLC Due to Recall initiated as a...

The Issue: Recall initiated as a precautionary measure due to potential risk of product...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2016· Pharmatech LLC

Recalled Item: Pedia D-Vite Drops Recalled by Pharmatech LLC Due to Recall initiated as a...

The Issue: Recall initiated as a precautionary measure due to potential risk of product...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2016· Pharmatech LLC

Recalled Item: Tri-Vitamin Recalled by Pharmatech LLC Due to Recall initiated as a...

The Issue: Recall initiated as a precautionary measure due to potential risk of product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2016· Becton Dickinson & Company

Recalled Item: BD 23 G x .75 in. BD Vacutainer¿ Push Button Recalled by Becton Dickinson &...

The Issue: BD has received multiple reports of units associated with the 23 G x .75 in....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Permits access...

The Issue: Shipping carton labeling error.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Calibrator U Recalled by Siemens Healthcare...

The Issue: Failure of analytical sensitivity with Calibrator U kit lots ending in 63...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Module Model 8110 with software version 9.15 The Recalled by...

The Issue: A software anomaly with the Alaris Syringe module software version 9.15 may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Arrow International Inc

Recalled Item: Arterial Line Catheterization Kit with Sharps Safety Features Permits access...

The Issue: Shipping carton labeling error.

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

Class II — Potential Health HazardOngoing
DrugAugust 5, 2016· Teva North America

Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America Due to...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 5, 2016· Medtronic Inc.

Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...

The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Riverpoint Medical, LLC

Recalled Item: Nylon Surgical Suture for human use and vet use Recalled by Riverpoint...

The Issue: Nylon Surgical Sutures are recalled because the seals may become open during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam and Symbia E gamma camera systems with patient beds Recalled by...

The Issue: "We have received reports of patients hair being caught in the e.cam and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Riverpoint Medical, LLC

Recalled Item: Polypropylene Surgical Sutures Recalled by Riverpoint Medical, LLC Due to...

The Issue: Polypropylene Surgical Sutures are recalled because the seals may become...

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

Class II — Potential Health HazardOngoing
DrugAugust 4, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Bupivacaine Hydrochloride Inj. Recalled by Hospira Inc., A Pfizer Company...

The Issue: Presence of particulate matter: Confirmed customer report for the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 4, 2016· Genzyme Corporation / Genzyme Biosurgery

Recalled Item: Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2016· Amerisource Health Services

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

The Issue: Failed dissolution specifications - the out of specification result for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 4, 2016· Terumo Medical Corp

Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...

The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2016· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...

The Issue: Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter...

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

Class II — Potential Health HazardOngoing