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. 2,650 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,650 in last 12 months

Showing 721740 of 28,140 recalls

Medical DeviceOctober 14, 2025· Beckman Coulter Ireland, Inc.

Recalled Item: BECKMAN COULTER BICARBONATE OSR6237 OSR6637 OSR6x37 Bicarbonate is Recalled...

The Issue: Bicarbonate reagent may generate falsely high Bicarbonate results due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: EVIS EXERA III Duodenovideoscope Product Name: Olympus TJF-Q190V...

The Issue: Continued reports of positive cultures and infections have identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2025· Becton Dickinson & Company

Recalled Item: BD Luer Tip Caps Recalled by Becton Dickinson & Company Due to BD has...

The Issue: BD has confirmed through internal testing that certain device trays failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2025· MRIMed Inc.

Recalled Item: MRI LED Mobile Exam Light Battery This non-magnetic Recalled by MRIMed Inc....

The Issue: Due to battery component overheating while charging resulting in melting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2025· Paragon 28, Inc.

Recalled Item: Phantom Fibula Nail Recalled by Paragon 28, Inc. Due to Fibula nail system...

The Issue: Fibula nail system intended for use in fixation of fibular fractures and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2025· Thoratec LLC

Recalled Item: CentriMag Blood Pump Recalled by Thoratec LLC Due to Acute circulatory...

The Issue: Acute circulatory support system pump may not fit into the motor and reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience Kit Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia circuit kit Recalled by Medline Industries, LP Due to Firm...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 9, 2025· C-RAD POSITIONING AB

Recalled Item: Brand Name: Catalyst+ Product Name: Catalyst Recalled by C-RAD POSITIONING...

The Issue: Due to issues with the system's stereotactic radiosurgery (SRS) treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Myofunctional Research Company USA

Recalled Item: Myosa for Kids KS1 /Sp/Mb/Mp/Lb/Lc KS2 /Sc/Mb/Mc/Mp/Lb/Lc Myosa Recalled by...

The Issue: Due to firm mistakenly distributing product within the U.S. without FDA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Pivotal Health Solutions, Inc.

Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...

The Issue: The heat function may become damaged over time due to patients pressing on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Pivotal Health Solutions, Inc.

Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...

The Issue: The heat function may become damaged over time due to patients pressing on...

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

Class II — Potential Health HazardOngoing