Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,580 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,580 in last 12 months

Showing 1172111740 of 28,140 recalls

Medical DeviceMay 8, 2020· Ge Healthcare

Recalled Item: The OEC 9900 C-Arm is designed to provide fluoroscopic and Recalled by Ge...

The Issue: GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2020· Merge Healthcare, Inc.

Recalled Item: Merge Healthcare Merge Application Server Software Release and Merge...

The Issue: An error in the calculation of the Michigan Ranges can generate an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Compression Screw Recalled by Stryker GmbH Due to Seal integrity of...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S Recalled by...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If an examination is interrupted when the InSpect Projection View (PV) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker 1 End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2020· Endologix, Inc.

Recalled Item: Ovation iX Abdominal Stent Graft Systems Recalled by Endologix, Inc. Due to...

The Issue: A material weakness adjacent to the polymer fill channel may become...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 5, 2020· Olympus Corporation of the Americas

Recalled Item: ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use...

The Issue: Products repaired with the incorrect service manual may be missing an O ring...

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

Class II — Potential Health HazardOngoing