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 2626126280 of 28,172 recalls

Medical DeviceMarch 8, 2013· Linde Gas North America Llc

Recalled Item: MEDICYCL-E- Lite Portable Oxygen System An integrated portable oxygen...

The Issue: A number of MEDICYL-e Portable Oxygen Systems may have misapplied valve flow...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Ormco/Sybronendo

Recalled Item: Bracket Buccal Tube U7L DB/UL22 Roth MT HK 0/-14/0 Product Recalled by...

The Issue: Ormco Corporation is voluntarily recalling one (1) lot of Bracket Buccal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes 3.5 MM LCP(R) Distal Humerus System The Synthes 3.5 Recalled by...

The Issue: Recall is being initiated due to the part being mislabeled (Part Number...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Spinal Solutions, LLC

Recalled Item: APLIF Implants and Instruments Recalled by Spinal Solutions, LLC Due to...

The Issue: Spinal Solutions is recalling the APLIF system because it is not supported...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: The PCA 3 system cam be used in a wide range of clinical settings Recalled...

The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: The LifeCare PCA Plus II infusion pump system is designed for safe Recalled...

The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: LifeCare PCA 3 Recalled by Hospira Inc. Due to Screw rotation error...

The Issue: Screw rotation error occurring when the pump detects a mismatch between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: LifeCare PCA infusion system with Hospira MedNet software allows clinicians...

The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: LifeCare PCA Infusion System with Hospira MedNet Software Recalled by...

The Issue: Screw rotation error occurring when the pump detects a mismatch between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: The LifeCare Pump Model 4200 PCA Infuser makes possible the Recalled by...

The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2013· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet Getinge Group battery modules for use with Maquet SERVO-i Recalled by...

The Issue: When using the SERVO-i on battery power, in a very small number of cases,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 7, 2013· US Endoscopy Group Inc

Recalled Item: Torrent" irrigation tubing. Product Usage: The Torrent irrigation system...

The Issue: The firm was notified by their customers that there was a water leakage from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2013· Maquet Cardiovascular, LLC

Recalled Item: MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version...

The Issue: It has come to the attention of MAQUET that there have been episodes of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Pro meters (catalog number 05530199160)bar code scanner. Used...

The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Alere San Diego, Inc.

Recalled Item: The Alere Cholestech LDX¿ high sensitivity C-Reactive Protein (hsCRP) Test...

The Issue: The Alere Cholestech LDX¿ hsCRP cassette (PN 12-807) may have increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Smith & Nephew Inc

Recalled Item: TRIGEN (TM) L-P SCREW Recalled by Smith & Nephew Inc Due to One batch of 4.5...

The Issue: One batch of 4.5 mm diameter Trigen Low-Profile Bone Screws were incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Inform II Blood Glucose Monitoring System bar code scanner....

The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX ALT AST Test Cassette Recalled by Alere San Diego, Inc....

The Issue: The recall was initiated because Alere San Diego has an update for the Alere...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Carefusion Corporation

Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...

The Issue: The recall was initiated because Carefusion has received reports of a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 6, 2013· Carefusion Corporation

Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...

The Issue: The recall was initiated because Carefusion has identified potential risk...

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

Class II — Potential Health HazardOngoing