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. 2,465 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,465 in last 12 months

Showing 2412124140 of 28,172 recalls

Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ANGIOGRAPHY PACK - ( 1) FEMORAL ANGlO. DRAPE WITH POUCH Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo Lab Data Manager Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: Certain configuration parameters may cause the ranges to not hold results as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Integra LifeSciences Corp.

Recalled Item: Accell Evo3C Demineralized Bone Matrix Recalled by Integra LifeSciences...

The Issue: This lot of Accell Evo3C Demineralized Bone Matrix, 5cc was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· KCI USA, Inc.

Recalled Item: CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number...

The Issue: Blade can shift during shipping which makes the product ineffective.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Small Bone Innovations

Recalled Item: Small Bone Innovations 3.0/4.0mm AutoFIX" Cannulated Compression Screw...

The Issue: Small Bone Innovations (SBi) is recalling all lots of 3.0/4.0mm AutoFIX"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: VerSys¿ Hip System Recalled by Zimmer, Inc. Due to During routine...

The Issue: During routine inspection, beaded hip stem forgings received from supplier...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2014· Ventlab LLC

Recalled Item: Manual Resuscitator Bag Series: AF1000 Recalled by Ventlab LLC Due to The...

The Issue: The pop-off valve in the defective devices remain open and a squeeze of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 16, 2014· Alcon Research, Ltd.

Recalled Item: Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part...

The Issue: Alcon CUSTOM-PAK which is supposed to contain a 27G Anterior Chamber Cannula...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2014· Nidek Inc

Recalled Item: GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser...

The Issue: Laser Aperture label was not applied to certain GYC-1000 Green Laser...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo RT Dosimetrist 2.7 system Product Usage: The intended Recalled...

The Issue: An update to the Virtual Simulation software of the syngo RT Dosimetrist is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing