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 2254122560 of 28,172 recalls

Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: FORTE (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Gemini GXL 16 Slice (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Extended Brilliance Workstation (Uninterruptible Power Supply (UPS)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Big Bore (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Flex (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: iCT SP (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF PET/CT 64 Slice (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 40 - Slices(Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity PET/MR (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: MX 16 Slice Phase II (Uninterruptible Power Supply (UPS) accessory Recalled...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 6 Slice Air (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Merge Healthcare, Inc.

Recalled Item: Merge LIS software. Recalled by Merge Healthcare, Inc. Due to There is a...

The Issue: There is a potential for duplicate container numbers to be created for patients.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· GE Healthcare

Recalled Item: GE Healthcare Millennium VG Recalled by GE Healthcare Due to GE Healthcare...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· SpineFrontier, Inc.

Recalled Item: SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique...

The Issue: The PedFuse Pedicle Screw Rod Caliper included with the MISquito Pedicle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Codman & Shurtleff, Inc.

Recalled Item: CODMAN 3000 Series Set- Huber needles. Used in combination Recalled by...

The Issue: Needle is leaking from hub/needle cannula connection

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS/HIT Set Advanced with Bioline and/or Softline Coating Console Product...

The Issue: A potential issue was detected that could result in blood leakage from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Quadrox-iD Adult Diffusion Membrane Oxygenator Product Usage: The Quadrox-iD...

The Issue: A potential issue was detected that could result in blood leakage from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2015· DePuy Orthopaedics, Inc.

Recalled Item: LCS COMPLETE RPS inserts Recalled by DePuy Orthopaedics, Inc. Due to The LCS...

The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2015· Ossur H / F

Recalled Item: LP Rotate Foot System prosthetic device for fitting lower extremity Recalled...

The Issue: The threads of the outer tube of the shock module of LP Rotate are too...

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

Class II — Potential Health HazardOngoing