Large Volume Abdominal Paracentesis Kit — Class II medical device recall Z-1297-2018
Terminated recall by Arrow International Inc, reported 2018-04-11. Product packaging may not be completely sealed.
| Recall number | Z-1297-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2017-10-24 |
| Classified | 2018-04-03 |
| Reported by FDA | 2018-04-11 |
| Terminated | 2020-04-17 |
| Quantity | 30,577 eaches |
Product
Large Volume Abdominal Paracentesis Kit
Reason for recall
Product packaging may not be completely sealed.
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-1297-2018. 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.