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. 2,429 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,429 in last 12 months

Showing 3546135480 of 49,744 recalls

Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLI V3.X TO V4.1 DL380 SERVER Product Usage: MYLA Recalled by...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLINIC PATCH 3.3.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD V4.1 CLI Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD V4.0 CLI Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
DrugNovember 2, 2015· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Meclizine Hydrochloride Tablets Recalled by Mylan Institutional, Inc....

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 2, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted...

The Issue: The firm has received 15 complaints over ten years related to the connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...

The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 2, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...

The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...

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

Class I — Serious Health HazardOngoing
DrugOctober 29, 2015· Amerisource Health Services

Recalled Item: HYDROCHLOROTHIAZIDE CAPSULES Recalled by Amerisource Health Services Due to...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Computed Tomography X-ray system Recalled by Philips...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: Perfusion scan feature may not be available on machines running software...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· NxStage Medical, Inc.

Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...

The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2015· NxStage Medical, Inc.

Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...

The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2015· Sanofi-Aventis U.S. LLC

Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: Defective Delivery System; potential to have inaccurate dosage delivery

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 28, 2015· Sanofi-Aventis U.S. LLC

Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: Defective Delivery System; potential to have inaccurate dosage delivery

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 28, 2015· BC Group International Inc

Recalled Item: DA-2006P - Defibrillator / Pacer Analyzer Recalled by BC Group International...

The Issue: Device is not functioning as intended: Two wires running to the ECG...

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

Class III — Low RiskOngoing