FDA Device recall Z-0606-2014
RTC 25-C Inline Aerosol Tee Adapter
- FDA Device
- Class II
- terminated
- Published 2014-01-08
On 2014-01-08 the FDA classified a Class II recall of RTC 25-C Inline Aerosol Tee Adapter by Instrumentation Industries, citing some packages of the RTC 25-C may have been shipped to customers with incomplete Installation and Usage Directions due to a printing error.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0606-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-11-13 |
| Published | 2014-01-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Instrumentation Industries |
| Distribution | US |
Product
RTC 25-C Inline Aerosol Tee Adapter. Intended to be used to adapt an aerosolized medication delivery system having an elliptical mouthpiece to a ventilator circuit.
Reason
Some packages of the RTC 25-C may have been shipped to customers with incomplete Installation and Usage Directions due to a printing error.
Identifiers
| code_info | multiple lots shipped between 10/7/13 and 11/6/13: P1002913, P1004413, P1005713, P1007713, P1009813, P1014213, P1014813, and P1102013. |
|---|
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-0606-2014%22
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