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McKesson

MCKESSON MEDICAL-SURGICAL INC. · Model 16-441 · UDI-DI 00612479280601

CBH
10
510(k) clearances
822
Adverse events (21 deaths)
12
Recalls
144
Facilities

Description

Trach tube holder, pediatric

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.