Arrow Endurance" Extended Dwell Peripheral Catheter System — Class II medical device recall Z-0837-2020
Terminated recall by Arrow International Inc, reported 2020-01-29, distributed in FL. Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System,
| Recall number | Z-0837-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2019-12-06 |
| Classified | 2020-01-22 |
| Reported by FDA | 2020-01-29 |
| Terminated | 2021-11-02 |
| Distributed | FL |
| Quantity | 575 |
| Reason classes | sterility |
| Lot numbers | 13F19E0247, 13F19F0006, 13F19G0433 |
| Model numbers | ASK-00820-FLH |
| Expiration dates | 2020-08-20 |
Product
Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH
Reason for recall
Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.
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-0837-2020. 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.