FDA Device recall Z-1238-2020
Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN
- FDA Device
- Class II
- terminated
- Published 2020-02-26
On 2020-02-26 the FDA classified a Class II recall of Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN by Arrow International, citing product lidstock contains the incorrect expiration date for the product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1238-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-20 |
| Published | 2020-02-26 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Arrow International |
| Distribution | US |
Product
Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN
Reason
Product lidstock contains the incorrect expiration date for the product
Identifiers
| code_info | Lot Number: 13F18K0740 |
|---|
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-1238-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.