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 1316113180 of 28,140 recalls

Medical DeviceAugust 19, 2019· RESPIRATORY THERAPEUTICS GROUP LLC

Recalled Item: RespVent Closed Suction System T-Piece Tracheostomy Adult Recalled by...

The Issue: It has been determined that some units of catheters were not tightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: Model No. 01-1503-0032 (Adolescent Nail Attachment Bolt). Component of the...

The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the...

The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing...

The Issue: Interference can occur between the adolescent attachment bolt and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 LEFTTriathlon Femoral...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 RIGHT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Return Patient Pads (10/ box) Model # 6050Pl used Recalled by...

The Issue: Discrepancy between the correct expiration dates on the individual pouches...

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

Class III — Low RiskOngoing
Medical DeviceAugust 16, 2019· IrriMAX Corporation

Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...

The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Bioseal Corporation

Recalled Item: Bioseal Trachea Extender 1/pl 50pk/Cs Recalled by Bioseal Corporation Due to...

The Issue: The reported stress crack in the port of the swivel elbow where the flip cap...

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

Class II — Potential Health HazardOngoing