FDA Device recall Z-0017-2013
Flow Meter, CM Assembly, Model #27025, Serial # 13686, 13690, 13712, 13793
- FDA Device
- Class I
- terminated
- Published 2012-10-17
On 2012-10-17 the FDA classified a Class I recall of Flow Meter, CM Assembly, Model #27025, Serial # 13686, 13690, 13712, 13793 by Accutron, citing accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it flows Nitrous Gas without Oxygen gas being turned on, it functions in an incorrect manner.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0017-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-04-29 |
| Published | 2012-10-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Accutron |
| Distribution | US |
Product
Flow Meter, CM Assembly, Model #27025, Serial # 13686, 13690, 13712, 13793. Flowmeter, CM Assembly, Model#31970, Serial#13692. Product Usage: Conscious Sedation Unit Analgesia Gas Machine.
Reason
Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it flows Nitrous Gas without Oxygen gas being turned on, it functions in an incorrect manner.
Identifiers
| code_info | Model#27025: Lot # 73971, 74929. Model#31970: Lot#74142. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0017-2013%22
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