ET-20 Anesthesia Extension Tubes — Class II medical device recall Z-0696-2016
Terminated recall by Global Healthcare Inc, reported 2016-02-10. Firm was notified of a potential product defect related to kinking (flattening) of anesthesia extension tubes
| Recall number | Z-0696-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Global Healthcare Inc, Alpharetta, GA, United States |
| Recall initiated | 2016-01-06 |
| Classified | 2016-02-03 |
| Reported by FDA | 2016-02-10 |
| Terminated | 2016-03-25 |
| Lot numbers | 1505201 |
Product
ET-20 Anesthesia Extension Tubes, 2.5 ml approximately, Sterile and Disposable, Wall Medical Inc., Made in China
Reason for recall
Firm was notified of a potential product defect related to kinking (flattening) of anesthesia extension tubes which may represent a potential health hazard.
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-0696-2016. 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.