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 3094130960 of 49,744 recalls

Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Bariatric Bed - BAR600IVC Recalled by Invacare Corporation Due to The...

The Issue: The junction box used in the bariatric bed may emit sparks and result in a fire.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...

The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· K2M, Inc

Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...

The Issue: Instruments were developed without adequate consideration given to the need...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2016· Shire PLC

Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules Recalled by Shire PLC Due...

The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles...

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

Class III — Low RiskOngoing
Refund
DrugDecember 1, 2016· Teva Pharmaceuticals USA

Recalled Item: Risedronate Sodium Delayed-release Tablets Recalled by Teva Pharmaceuticals...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 1, 2016· Merit Medical Systems, Inc.

Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...

The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2016· Pride Mobility Products Corp

Recalled Item: TRU-Balance 3 Power Positioning Systems Recalled by Pride Mobility Products...

The Issue: The interface between the TB3 back and tilt base can separate when tilted...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· AtriCure, Inc.

Recalled Item: AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A...

The Issue: A complaint of the PRO2 jaw breaking prior to surgery being performed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-010-040 4.0MM Round Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8470-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
FoodNovember 30, 2016· Dolce Dolci LLC dba Villa Dolce Gelato

Recalled Item: Strawberry Gelato Recalled by Dolce Dolci LLC dba Villa Dolce Gelato Due to...

The Issue: Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 30, 2016· Dolce Dolci LLC dba Villa Dolce Gelato

Recalled Item: Strawberry Sorbet Recalled by Dolce Dolci LLC dba Villa Dolce Gelato Due to...

The Issue: Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical 400 Series Express Drains as follows: 4000-100N Express...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Dual Chamber Ocean Drains as follows: 2020-000 Ocean Recalled...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing