FDA Device recall Z-0837-2020
Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH
- FDA Device
- Class II
- terminated
- Published 2020-01-29
On 2020-01-29 the FDA classified a Class II recall of Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH by Arrow International, citing potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0837-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-06 |
| Published | 2020-01-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Arrow International |
| Distribution | FL |
Product
Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH
Reason
Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.
Identifiers
| code_info | REF: ASK-00820-FLH Manufacturing Lots: 13F19E0247, 13F19F0006, and 13F19G0433 Exp. Date: Aug. 2020 - Sep. 2020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0837-2020%22
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