MAQUET Servo Humidifier 163 — Class II medical device recall Z-2683-2016
Terminated recall by Teleflex Medical, reported 2016-09-07, distributed in FL, KS, WV. Cracking may occur at the 15mm and 22mm ISO female connector.
| Recall number | Z-2683-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Morrisville, NC, United States |
| Recall initiated | 2015-12-03 |
| Classified | 2016-08-29 |
| Reported by FDA | 2016-09-07 |
| Terminated | 2017-01-24 |
| Distributed | FL, KS, WV |
| Quantity | 2,700 units |
| Reason classes | packaging |
| Lot numbers | 201450, 201451, 201452, 201504, 2577 |
| Model numbers | 01-06-8125-8 |
Product
MAQUET Servo Humidifier 163, Inmed Mfg. Sdn. Bhd. Lot PT 2577, Jalan Perusahaan, 4, 34600 Kamunting, Perak, Malaysia.
Reason for recall
Cracking may occur at the 15mm and 22mm ISO female connector.
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-2683-2016. 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.