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 1188111900 of 28,140 recalls

Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Hip Products Item Number: 1) 110010462 RingLoc Hip System Recalled by...

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Knee Products: 141356 Regenerex Series-A Patella 3 Peg Recalled by Biomet,...

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Image-Intensified Fluoroscopic X-Ray System Recalled by Siemens...

The Issue: The unplugging of the main cable on the monitor trolley from the X10...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Knee Products: 183742 Vanguard Knee System Recalled by Biomet, Inc. Due to...

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2020· Becton Dickinson & Company

Recalled Item: BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553)...

The Issue: This product has been confirmed to exhibit holes in the packaging, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2020· Elekta Inc

Recalled Item: Elekta MONACO RTP Sytem Recalled by Elekta Inc Due to The Monaco RTP...

The Issue: The Monaco RTP Radiation Treatment Planning System may change the shape and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2020· C.R. Bard Inc

Recalled Item: SureStep Foley Tray System - Product Usage: Intended for use Recalled by...

The Issue: There is potential for a white paper-type residue attached to the catheter.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2020· Becton Dickinson & Co.

Recalled Item: BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Recalled by...

The Issue: May exhibit increased levels of artifacts which could be difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2020· Becton Dickinson & Co.

Recalled Item: BD BBLTM Gram Crystal Violet 3.8L-- IVD Primary stain for Recalled by Becton...

The Issue: May exhibit increased levels of artifacts which could be difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2020· Becton Dickinson & Co.

Recalled Item: BD BBLTM Gram Stain Kit with Stabilized Iodine-- IVD For Recalled by Becton...

The Issue: May exhibit increased levels of artifacts which could be difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing