Arrow — Class II medical device recall Z-2170-2017
Terminated recall by Arrow International Inc, reported 2017-06-07, distributed in NC. Arrow International is notifying each customer who received the affected that product that the kits do not con
| Recall number | Z-2170-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2017-04-28 |
| Classified | 2017-05-26 |
| Reported by FDA | 2017-06-07 |
| Terminated | 2018-08-03 |
| Distributed | NC |
| Quantity | 3,918 units |
| Lot numbers | 23F15L0593, 23F15L0662, 23F16A0298, 23F16A0300, 23F16B0028, 23F16B0338, 23F16B0523, 23F16C0321, 23F16C0632, 23F16J0105, 23F16J0151, 23F16K0363, 23F16K0431, 23F16K0449, 23F16K0820 |
Product
Arrow(R) VPS(R) Access Kit for use with 4 and 5 Fr. Peripherally Inserted Central Venous Catheters
Reason for recall
Arrow International is notifying each customer who received the affected that product that the kits do not contain important information regarding the 3M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing.
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-2170-2017. 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.