Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,482 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,482 in last 12 months

Showing 2188121900 of 27,373 recalls

Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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 LXL 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· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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· 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 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· 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 4, 2015· Cardiovascular Systems, Inc.

Recalled Item: Diamondback 360 Coronary Orbital Atherectomy System Recalled by...

The Issue: The OAD saline sheath outer layer may flake off from the catheter due to...

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

Class I — Serious 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
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