McKesson Insulin Syringe 0 — Class II medical device recall Z-0119-2019
Terminated recall by Cypress Medical Products LLC, reported 2018-10-24, distributed nationwide. Small hole at the end of the syringe is impeding suction of liquid.
| Recall number | Z-0119-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cypress Medical Products LLC, Richmond, VA, United States |
| Recall initiated | 2018-09-04 |
| Classified | 2018-10-16 |
| Reported by FDA | 2018-10-24 |
| Terminated | 2024-05-28 |
| Distributed | Nationwide (US) |
| Quantity | 400 cases |
| Lot numbers | KSH0603 |
| Model numbers | 102-SN310C31516P |
Product
McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P Product Usage: Indication of Use: Injection of U-100 insulin only.
Reason for recall
Small hole at the end of the syringe is impeding suction of liquid.
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-0119-2019. 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.