Arrow Pressure Injectable PICC Kit Catheter — Class II medical device recall Z-2338-2017
Terminated recall by Arrow International Inc, reported 2017-06-21, distributed nationwide. The Arrow Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central ve
| Recall number | Z-2338-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2017-05-09 |
| Classified | 2017-06-12 |
| Reported by FDA | 2017-06-21 |
| Terminated | 2018-09-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
Product
Arrow Pressure Injectable PICC Kit Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days The Arrow Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling.
Reason for recall
The Arrow Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling.
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-2338-2017. 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.