Stryker FlowPort II Adapter: Model number: 00CAT00778 The FlowPort II… — Class II medical device recall Z-1910-2016
Terminated recall by Stryker Corporation, reported 2016-06-15, distributed in GA, MD, MT, NJ, UT. Complaints were received for the Stryker FlowPort II Adapter, and investigation found that the scope sat in th
| Recall number | Z-1910-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Corporation, San Jose, CA, United States |
| Recall initiated | 2016-05-04 |
| Classified | 2016-06-03 |
| Reported by FDA | 2016-06-15 |
| Terminated | 2016-06-03 |
| Distributed | GA, MD, MT, NJ, UT |
| Quantity | 21 units |
| Model numbers | 00CAT00778 |
Product
Stryker FlowPort II Adapter: Model number: 00CAT00778 The FlowPort II Adapter is intended to connect the FlowPort II Cannulas to commercially available, 4mm arthroscopes in surgical procedures.
Reason for recall
Complaints were received for the Stryker FlowPort II Adapter, and investigation found that the scope sat in the adapter 180 degrees in the wrong direction
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-1910-2016. 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.