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. 2,455 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,455 in last 12 months

Showing 2220122220 of 49,150 recalls

Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Standard Starter Set with and without Service Gas (2 Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer (reloadable) [9 pcs] - Product Usage: Is Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Becton Dickinson & Company

Recalled Item: CareFusion MaxPlus Clear Needleless Connector. Intended for Positive...

The Issue: After disconnection of a luer, the valve of the connector remains recessed;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer Insert [5 pcs - Product Usage: is Recalled by SenTec...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer Set (1 charger plus 1 insert) - Recalled by SenTec...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Neonatal Starter Set with and without Service Gas (2 Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2019· Abbott Laboratories, Inc

Recalled Item: ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Recalled by...

The Issue: Mixer blade may separate from mixer due to the screw and nut failure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2019· Abbott Vascular

Recalled Item: Abbott MitraClip XTR Clip Delivery System Recalled by Abbott Vascular Due to...

The Issue: Reports of implantable mitral valve repair system clips unexpectedly opening...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2019· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and...

The Issue: The 0-arm 1000 Imaging System uses energy from the batteries to generate...

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

Class II — Potential Health HazardOngoing
FoodMay 1, 2019· U.S. Tov, Inc.

Recalled Item: Dragonfly Dehydrate Guava Ing: Guava Recalled by U.S. Tov, Inc. Due to...

The Issue: Undeclared sulfites.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
DrugApril 30, 2019· Par Pharmaceutical, Inc.

Recalled Item: Mycophenolate Mofetil for Injection Recalled by Par Pharmaceutical, Inc. Due...

The Issue: Presence of Particulate Matter; glass fragment observed in one vial of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 30, 2019· Sagent Pharmaceuticals Inc

Recalled Item: Ketorolac Tromethamine Injection Recalled by Sagent Pharmaceuticals Inc Due...

The Issue: Lack of Sterility Assurance: Microbial growth detected during a routine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject" 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing