MINI STICK MAX 5F X 10 CM STIFF — Class II medical device recall Z-1341-2024
Ongoing recall by Angiodynamics, Inc., reported 2024-03-27, distributed nationwide. Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure.
| Recall number | Z-1341-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics, Inc., Queensbury, NY, United States |
| Recall initiated | 2024-01-30 |
| Classified | 2024-03-21 |
| Reported by FDA | 2024-03-27 |
| Distributed | Nationwide (US) |
| Quantity | 5,840 units |
| UPC / GTIN / UDI-DI | 15051684023023 |
| Lot numbers | 5789493, 5789494, 5789495, 5789496, 5789497, 5791596, 5791597, 5791598, 5793392, 5793393, 5794602, 5794603, 5794604, 5794605, 5794606, 5795874, 5795875, 5797457, 5797458, 5797466, 5797467, 5798837, 5798843, 5798844 |
| Model numbers | 45-759 |
Product
MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759
Reason for recall
Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
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-1341-2024. 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.