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. 2,535 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,535 in last 12 months

Showing 1950119520 of 28,172 recalls

Medical DeviceJuly 12, 2016· Mckesson Medical Imaging Group

Recalled Item: McKesson Radiology Recalled by Mckesson Medical Imaging Group Due to The...

The Issue: The STAT priority icon was not displayed in the Study List when the study...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2016· Resmed Corporation

Recalled Item: Quattro Air FFM MED  AMER Recalled by Resmed Corporation Due to Masks in...

The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2016· ELITech Group B.V.

Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...

The Issue: Software malfunction; The action being taken due to the device becoming...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2016· Bausch & Lomb Inc Irb

Recalled Item: Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED Recalled by Bausch & Lomb Inc...

The Issue: Possible dull knife edge

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Bausch & Lomb Inc Irb

Recalled Item: Laseredge 1.1mm Arrow Knife Angled Recalled by Bausch & Lomb Inc Irb Due to...

The Issue: Possible dull knife edge

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Testing System Model Number: 0200431...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....

The Issue: The product lot failed to meet QC acceptance criteria during stability...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: INRatio Prothrombin Time (PT) Monitoring System Model Number: 0100007...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· American National Mfg Inc

Recalled Item: Panacea Air Pro Mattress Control Unit Recalled by American National Mfg Inc...

The Issue: The Panacea Air Pro Mattress Control Unit is being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio/ INRatio2 PT/INR Test Strips Model Number: 99007EU Recalled by...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR Test Strips Model Number: 0100071 Recalled by Alere San...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR System Professional Model Numbers: 0100004 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Home Monitoring System Model Number: 0200432 Recalled...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Straight Spatula Electrode 36C Item Code: E277036 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Argon Sharp Needle Electrode 28CM Item Code: E258228...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 3" Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 36CM Item Code: E277236 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing