Arrow Select Kits — Class III medical device recall Z-1030-2015
Terminated recall by Arrow International Inc, reported 2015-02-04, distributed nationwide. Certain product codes and lot numbers of Kits with Biopatch Dressing were packaged with the incorrect size Bio
| Recall number | Z-1030-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2015-01-09 |
| Classified | 2015-01-29 |
| Reported by FDA | 2015-02-04 |
| Terminated | 2017-08-23 |
| Distributed | Nationwide (US) |
| Quantity | 4,484 |
| Lot numbers | 23F14H0501, 23F14H0577, 23F14H0918, 23F14H1120, 23F14J0237, 23F14J0287, 23F14J0356, 23F14J0508, 23F14J0554, 23F14J0613, 23F14J0617, 23F14J0619, 23F14J1134, 23F14J1142, 23F14J1355, 23F14J1390, 23F14J1433, 23F14J1516, 23F14J1551, 23F14K0114, 23F14K0115 |
Product
Arrow Select Kits (ASK), Maximal Barrier Precautions Kits (CDC) and Arterial Catheterization Kit (NA) with Biopatch Dressing
Reason for recall
Certain product codes and lot numbers of Kits with Biopatch Dressing were packaged with the incorrect size Biopatch Dressing. No risk to patients is anticipated.
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-1030-2015. 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.