AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number:… — Class I medical device recall Z-2096-2016
Terminated recall by Stryker Sustainability Solutions, reported 2016-07-27, distributed in CA, CT, MA, MD, NY, PA, TX, UT…. Product defect; tip of two (2) Angiographic Catheters model # 10732203 broke off, prior to being used on the
| Recall number | Z-2096-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Sustainability Solutions, Tempe, AZ, United States |
| Recall initiated | 2016-06-01 |
| Classified | 2016-07-21 |
| Reported by FDA | 2016-07-27 |
| Terminated | 2016-10-19 |
| Distributed | CA, CT, MA, MD, NY, PA, TX, UT, VA, VT, WA |
| Countries outside the US | CA |
| Quantity | 167 |
| Model numbers | 10732203 |
Product
AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203
Reason for recall
Product defect; tip of two (2) Angiographic Catheters model # 10732203 broke off, prior to being used on the patient.
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-2096-2016. 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.