FDA Device recall Z-1927-2017
Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consistin…
- FDA Device
- Class II
- terminated
- Published 2017-05-10
On 2017-05-10 the FDA classified a Class II recall of Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consistin… by Dale Medical Products, citing ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1927-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-24 |
| Published | 2017-05-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Dale Medical Products |
| Distribution | US |
Product
Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consisting of an adhesive base, Dale product number 273, that attaches to the patient's skin and a cushioned neckband with tube channel that attaches with hook & loop closures. The 270 is used to secure and stabilize endotracheal tubes, preventing unnecessary movement which can help prevent accidental .extubation
Reason
ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.
Identifiers
| code_info | Lot Numbers: 02 23 16, 04 11 16, 05 11 16, 02 24 16 , 04 19 16 , 05 13 16, 03 04 16, 04 20 16 ,…Lot Numbers: 02 23 16, 04 11 16, 05 11 16, 02 24 16 , 04 19 16 , 05 13 16, 03 04 16, 04 20 16 , 05 16 16, 03 07 16, 04 21 16, 05 18 16, 03 08 16, 05 03 16 , 05 20 16, 03 10 16 , 05 05 16, 05 24 16, 03 11 16 , 05 06 16 , 05 26 16, 04 07 16, 05 09 16 , 05 31 16, 04 08 16, 05 10 16 , 06 02 16 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1927-2017%22
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