VersaSafe Plastic Cannula — Class II medical device recall Z-3030-2017
Terminated recall by CareFusion 303, Inc., reported 2017-08-23, distributed in CO, IL, IN, MD, MI, NY, OH, TX. Punctures in blister packaging that was detected during the packaging process.
| Recall number | Z-3030-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CareFusion 303, Inc., San Diego, CA, United States |
| Recall initiated | 2017-06-30 |
| Classified | 2017-08-11 |
| Reported by FDA | 2017-08-23 |
| Terminated | 2021-02-03 |
| Distributed | CO, IL, IN, MD, MI, NY, OH, TX |
| Countries outside the US | AU, JP, NZ |
| Quantity | 1,546,800 units |
| Lot numbers | 1470303001, 1470303002, 1470304601, 1470306301, 1470306602, 1470311301, 1470311302, 1470314801, 1570314802, 1570317701, 1570317702, 1570317703, 1570317704, 1570322001, 1660771501 |
| Model numbers | 9391-0200 |
Product
VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.
Reason for recall
Punctures in blister packaging that was detected during the packaging process.
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-3030-2017. 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.