Arrow EPIDURAL NEEDLE COMPONENT AN-05505 — Class II medical device recall Z-1244-2020
Terminated recall by Arrow International Inc, reported 2020-02-26, distributed nationwide. Product lidstock contains the incorrect expiration date for the product
| Recall number | Z-1244-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2019-12-20 |
| Classified | 2020-02-14 |
| Reported by FDA | 2020-02-26 |
| Terminated | 2021-02-25 |
| Distributed | Nationwide (US) |
| Quantity | 1,839 |
| Reason classes | labeling |
| Lot numbers | 13F17L0441, 13F18H0836, 13R17L0441 |
Product
Arrow EPIDURAL NEEDLE COMPONENT AN-05505
Reason for recall
Product lidstock contains the incorrect expiration date for the product
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-1244-2020. 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.