FDA Device recall Z-2683-2016
MAQUET Servo Humidifier 163, Inmed Mfg
- FDA Device
- Class II
- terminated
- Published 2016-09-07
On 2016-09-07 the FDA classified a Class II recall of MAQUET Servo Humidifier 163, Inmed Mfg by Teleflex Medical, citing cracking may occur at the 15mm and 22mm ISO female connector.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2683-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-12-03 |
| Published | 2016-09-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Teleflex Medical |
| Distribution | FL, KS, WV |
Product
MAQUET Servo Humidifier 163, Inmed Mfg. Sdn. Bhd. Lot PT 2577, Jalan Perusahaan, 4, 34600 Kamunting, Perak, Malaysia.
Reason
Cracking may occur at the 15mm and 22mm ISO female connector.
Identifiers
| code_info | Model number: 01-06-8125-8, Product code: XKC01-06-8125-8, Lot numbers: 201450, 201451, 201452 and 201504. |
|---|
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-2683-2016%22
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