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 3072130740 of 49,744 recalls

Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number...

The Issue: Maquet has received 3 confirmed complaints related to the Li-lon Battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: The intended use listed in the English and localized language IFUs for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X upgraded to XCT 882454 Recalled by Philips Medical Systems...

The Issue: The intended use listed in the English and localized language IFUs for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Elekta, Inc.

Recalled Item: Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation...

The Issue: Cross profile for Varian 60 degree wedge shows "horns."

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2016· Tosoh Smd Inc

Recalled Item: Keyspan High-High Speed USB to Serial Adapter Product Usage: The Recalled by...

The Issue: Power outages causes reporting software to shutdown.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2016· Mako Surgical Corporation

Recalled Item: MAKO RIO THA Application User Guides Recalled by Mako Surgical Corporation...

The Issue: Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2016· AGFA Healthcare Corp.

Recalled Item: IMPAX Cardiovascular The IMPAX CV Reporting module consists of a Recalled by...

The Issue: A customer experienced when using IMPAX CV Reporting software, specifically,...

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2016· Sandoz Incorporated

Recalled Item: Nadolol Tablets Recalled by Sandoz Incorporated Due to Failed dissolution...

The Issue: Failed dissolution specification: recalled due to an out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2016· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: TEMAZEPAM CAPSULES USP Recalled by Vintage Pharmaceuticals LLC, DBA...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
DrugDecember 22, 2016· Roxane Laboratories, Inc.

Recalled Item: Furosemide Tablets USP Recalled by Roxane Laboratories, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: An unusually thick tablet was reported...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2016· Aurobindo Pharma USA Inc

Recalled Item: Venlafaxine Hydrochloride extended release capsules Recalled by Aurobindo...

The Issue: Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 22, 2016· Schreiber Food International

Recalled Item: Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce Net 128 Fl. Oz....

The Issue: Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2016· Rich Products Corp

Recalled Item: Jon Donaire Ice Cream Layer Cake Recalled by Rich Products Corp Due to...

The Issue: The product may contain undeclared walnuts from intermediate layer cake...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2016· Rich Products Corp

Recalled Item: Jon Donaire Ice Cream Layer Cake Recalled by Rich Products Corp Due to...

The Issue: The product may contain undeclared walnuts from intermediate layer cake...

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

Class II — Potential Health HazardOngoing
Refund