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NeoBar®

Neotech Products LLC · Model Jumbo Hydrocolloid · UDI-DI 10812594010993

CBH Prescription
10
510(k) clearances
827
Adverse events (21 deaths)
12
Recalls
144
Facilities

Description

The NeoBar is intended to secure an endotracheal tube. It is intended for use on pediatric (neonates, infants and children) patients.

Recalls

DateFirmReason
2024-12-23Hollister IncorporatedHollister received reports of decreased skin barrier wear time which could can lead to tube migration
2024-12-23Hollister IncorporatedHollister received reports of decreased skin barrier wear time which could can lead to tube migration
2024-12-23Hollister IncorporatedHollister received reports of decreased skin barrier wear time which could can lead to tube migration
2024-12-23Hollister IncorporatedHollister received reports of decreased skin barrier wear time which could can lead to tube migration
2024-11-18MEDLINE INDUSTRIES, LP - NorthfieldComplaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbones and upper lip wh
2024-11-18MEDLINE INDUSTRIES, LP - NorthfieldComplaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbones and upper lip wh
2024-11-18MEDLINE INDUSTRIES, LP - NorthfieldComplaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbones and upper lip wh
2024-11-18MEDLINE INDUSTRIES, LP - NorthfieldComplaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbones and upper lip wh
2017-03-24Dale Medical Products, Inc.ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.
2017-03-24Dale Medical Products, Inc.ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.