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 3238132400 of 49,744 recalls

Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330BR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450BR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330NR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Cepheid

Recalled Item: Xpert MRSA Catalog GXMRSA-120 Recalled by Cepheid Due to Internal...

The Issue: Internal investigation found the certain lots of MRSA kits have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) Recalled by Becton, Dickinson...

The Issue: Internal review found that some vials of CD3/CD4/CD45 state that the product...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: S7 MACH FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Cranial S7. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Fusion ENT Application. The software application is sent in CD Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Spine. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH AxiEM Cranial Treon. The software application is sent in Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH Cranial Treon. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
FoodJuly 16, 2016· ConAgra Frozen Foods, Inc

Recalled Item: PF Chang's Home Menu Brand Shrimp Lo Mein Recalled by ConAgra Frozen Foods,...

The Issue: Metal fragments were discovered in an raw ingredient used in the manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2016· The Harvard Drug Group

Recalled Item: Diocto Liquid (docusate sodium) 50 mg/5 mL Stool Softener Laxative Recalled...

The Issue: Microbial contamination of Non-Sterile Products; positive findings of...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 15, 2016· Teva North America

Recalled Item: Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol Recalled...

The Issue: Failed Content Uniformity Specifications: out of specification test result...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Roche/Hitachi MODULAR Analytics Combination Systems Modular D/P: Clinical...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 471 centrifuge unit calculator/data processing module Recalled by...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 701 Post-Analytical Unit calculator/data processing module Recalled...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: VS II Aliquoter System calculator/data processing module Recalled by Roche...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: URISYS 2400 Urine Analyzer Automated Urinalysis System Product Usage: The...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing