MAQUET Servo Humidifier 163 recall
MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser (artificial nose) is a device…
Why was MAQUET Servo Humidifier 163 recalled?
Connector mount cracks which may lead to a leak failure during use and necessitate immediate replacement in the breathing circuit. If leak exists and is left untreated, patient may be deprived of adequate anesthetic gases over a period of time and serious adverse health consequences may occur.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Batch Numbers: 201321, 201323, and 201324.
- Product
- MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser (artificial nose) is a device…
- Recalling firm
- Teleflex, Inc.
- Quantity
- 18
- Distribution
- Distributed in the states of FL, MI, WV, and KS.
- Recall date
- February 18, 2015
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)