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 1958119600 of 28,172 recalls

Medical DeviceJune 28, 2016· Medtronic Xomed, Inc.

Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to Wire in...

The Issue: Wire in tubing can become exposed, posing potential harm to the intubated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· CHG Hospital Beds Inc

Recalled Item: Spirit Select Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical...

The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Trumpet Handpiece only Recalled by ConMed Corporation Due to The...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece Y-Tubing set Recalled by ConMed...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· Cardinal Health

Recalled Item: The 9025TRU Arterial Blood Gas (ABG) Kit is used to Recalled by Cardinal...

The Issue: Arterial Blood Gas (ABG) Kit- Missing Safety Component. The ABG Kit(s) have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Trumpet Handpiece with 5mm x 32cm Length Probe Recalled by ConMed...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· Moller Vital

Recalled Item: Molift Air 205 Recalled by Moller Vital Due to Potential for the bolt on the...

The Issue: Potential for the bolt on the suspension coupling on the Molift Air to come...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 2.3MM Tapered Router Recalled by Stryker Instruments Div. of Stryker...

The Issue: A variation in flute depth on the routers was observed. The variation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· The Anspach Effort, Inc.

Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...

The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· The Anspach Effort, Inc.

Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...

The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2016· Baxter Healthcare Corp.

Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...

The Issue: Baxter is issuing a safety alert in response to postmarketing reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2016· Cook Inc.

Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide Recalled by Cook Inc. Due to...

The Issue: Potential coating contamination with glass particles.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 23, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Incorrect...

The Issue: Incorrect values for the volume calculation. Software update VB30B via...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· Varian Medical Systems, Inc.

Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...

The Issue: Varian Medical Systems has received reports that unintended changes were...

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

Class II — Potential Health HazardOngoing