Multi-Lumen Central Venous Catheterization Kit — Class II medical device recall Z-0076-2015
Terminated recall by Arrow International Inc, reported 2014-10-22, distributed in CA, IN, KY, LA, MD, NC, NV, NY…. Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 be
| Recall number | Z-0076-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2014-09-18 |
| Classified | 2014-10-16 |
| Reported by FDA | 2014-10-22 |
| Terminated | 2014-12-02 |
| Distributed | CA, IN, KY, LA, MD, NC, NV, NY, OH, PA |
| Quantity | 65 |
| Reason classes | labeling |
| Lot numbers | RF3039028 |
Product
Multi-Lumen Central Venous Catheterization Kit
Reason for recall
Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.
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-0076-2015. 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.