Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The… — Class II medical device recall Z-1927-2017
Terminated recall by Dale Medical Products, Inc., reported 2017-05-10, distributed nationwide. ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the
| Recall number | Z-1927-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dale Medical Products, Inc., Plainville, MA, United States |
| Recall initiated | 2017-03-24 |
| Classified | 2017-05-03 |
| Reported by FDA | 2017-05-10 |
| Terminated | 2018-05-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA, CR, EC, GT, HK, ID, IE, IS, IT, MY, NO, PA, PY, SA |
| Quantity | 34,770 total |
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 for recall
ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1927-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.