ARROWg+ard Blue Plus Multi Lumen CVC — Class II medical device recall Z-0656-2018
Terminated recall by Arrow International Inc, reported 2018-02-28, distributed nationwide. These finished good kits may contain the incorrect Springwire Guide (SWG).
| Recall number | Z-0656-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2017-10-17 |
| Classified | 2018-02-20 |
| Reported by FDA | 2018-02-28 |
| Terminated | 2020-04-14 |
| Distributed | Nationwide (US) |
| Quantity | 5,926 total |
| Lot numbers | 13F16M0264, 13F17C0102 |
| Expiration dates | 2018-02-20 |
Product
ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter); Product Code: AK-45703-ACDC; Exp. Dates Feb 2018 - Nov 2018
Reason for recall
These finished good kits may contain the incorrect Springwire Guide (SWG).
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-0656-2018. 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.