Drug recall
Stryker FlowPort II Adapter: Model number: 00CAT00778 The FlowPort II Adapter is intended to connect the…
FDA recall event 74070 · Class II · Stryker Corporation
Key facts
| Event ID | 74070 |
|---|---|
| Recall numbers | Z-1910-2016 |
| Recalling firm | Stryker Corporation |
| Product type | Devices |
| Products | 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. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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 |
| Initiation date | May 4, 2016 |
| Report date | Jun 15, 2016 |
| Termination date | Jun 3, 2016 |
| City | San Jose |
| State | CA |
| Country | United States |
| FEI number | 2936485 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: