ASK-05501-AFH1 — Class II medical device recall Z-0114-2015
Terminated recall by Arrow International Inc, reported 2014-10-29, distributed in UT. Arrow International, Inc. is notifying customers that lot 23F13K0969 of product code ASK-05501-AFH1 contains a
| Recall number | Z-0114-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2014-09-15 |
| Classified | 2014-10-22 |
| Reported by FDA | 2014-10-29 |
| Terminated | 2015-12-18 |
| Distributed | UT |
| Quantity | 300 |
| Reason classes | foreign material |
| Lot numbers | 23F13K0969 |
| Model numbers | ASK-05501-AFH1 |
Product
ASK-05501-AFH1, Lot Number 23F13K0969 Anesthesia Conduction Catheter, Epidural Anesthesia Kit
Reason for recall
Arrow International, Inc. is notifying customers that lot 23F13K0969 of product code ASK-05501-AFH1 contains an incorrect component. The lidstock indicates that the kit contains one Syringe, 10mL, Luer-Slip Loss of Resistance, Glass but contains one Syringe, 10mL, Luer-Lock Loss of Resistance, Glass.
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-0114-2015. 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.