Walrus Arterial Embolectomy Catheter The arterial embolectomy… — Class II medical device recall Z-2911-2016
Terminated recall by Arrow International Inc, reported 2016-10-12, distributed nationwide. Arrow is recalling due to incorrect labeling of products.
| Recall number | Z-2911-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2016-07-07 |
| Classified | 2016-09-30 |
| Reported by FDA | 2016-10-12 |
| Terminated | 2017-10-25 |
| Distributed | Nationwide (US) |
| Quantity | 2,425 catheters |
| Reason classes | labeling |
| Lot numbers | 14F14E0300, 14F14J0155, 14F15A0174, 14F15B0244, 14F15D0197, 14F15E0263, 14F15F0406, 14F15G0347, 14F15G0348, 14F15G0349, 14F15H0025, 14F15H0251, 14F15H0258, 14F15H0261, 14F15H0292, 14F15H0332, 14F15J0139, 14F15J0363, CF2079921, CF2125865, CF3016366 |
Product
Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is intended for use in removing arterial emboli.
Reason for recall
Arrow is recalling due to incorrect labeling of products.
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-2911-2016. 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.