RTC 25-C Inline Aerosol Tee Adapter — Class II medical device recall Z-0606-2014
Terminated recall by Instrumentation Industries Inc, reported 2014-01-08, distributed nationwide. Some packages of the RTC 25-C may have been shipped to customers with incomplete Installation and Usage Direct
| Recall number | Z-0606-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Instrumentation Industries Inc, Bethel Park, PA, United States |
| Recall initiated | 2013-11-13 |
| Classified | 2013-12-29 |
| Reported by FDA | 2014-01-08 |
| Terminated | 2014-07-09 |
| Distributed | Nationwide (US) |
| Quantity | 220 |
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 for recall
Some packages of the RTC 25-C may have been shipped to customers with incomplete Installation and Usage Directions due to a printing error.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0606-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.