Teleflex Medical recalls MAQUET Servo Humidifier 163, Inmed Mfg. Sdn. Bhd. Lot PT 2577, Jalan Perusahaan, 4, 34600 Kamunting, Perak, Malaysia.
- Recall date
- December 3, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2683-2016
- FDA classification
- Class II
- Brand / firm
- Teleflex Medical
- Sold / distributed
- US Distribution to the states of : FL, KS, and WV.
Why it was recalled
Cracking may occur at the 15mm and 22mm ISO female connector.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
MAQUET Servo Humidifier 163, Inmed Mfg. Sdn. Bhd. Lot PT 2577, Jalan Perusahaan, 4, 34600 Kamunting, Perak, Malaysia.
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