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. 2,489 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,489 in last 12 months

Showing 2240122420 of 28,172 recalls

Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Round Drain with Trocar Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Ambulating Bulb Ambulating Bulb: The Ambulating Bulb comprises four main...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/8 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Lumenis Limited

Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....

The Issue: Device software treatment preset parameters for the XC treatment handpiece...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· CSA Medical

Recalled Item: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device...

The Issue: TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...

The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...

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

Class III — Low RiskOngoing
Medical DeviceMarch 24, 2015· The Anspach Effort, Inc.

Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...

The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...

The Issue: Customer reports that the ventilator display can freeze. Ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Philips Electronics North America Corporation

Recalled Item: Philips DigitalDiagnost Release 4.0.3 Recalled by Philips Electronics North...

The Issue: The system is designed to emit a beep upon termination of an exposure....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Lipase Reagent Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens internal investigation confirmed that current contamination...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems Recalled by...

The Issue: Medtronic is conducting a voluntary recall of all former Covidien Trellis 6...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Homocysteine test system - Homocysteine Reagent. 05385415190 Recalled by...

The Issue: Customers complained about under-recovery of non-Roche controls and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8 Recalled by...

The Issue: Edwards Lifesciences is recalling Fem-Flex II Pediatric Femoral Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2015· CooperSurgical, Inc.

Recalled Item: Carter-Thomason II Port Closure System Recalled by CooperSurgical, Inc. Due...

The Issue: The pad printing around the suture entry holes on the 15mm Suture Guide...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2015· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...

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

Class II — Potential Health HazardOngoing