McKesson Syringe 60CC — Class II medical device recall Z-2940-2024
Ongoing recall by Cypress Medical Products LLC, reported 2024-09-04, distributed nationwide. Affected syringes lack FDA clearance.
| Recall number | Z-2940-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cypress Medical Products LLC, Richmond, VA, United States |
| Recall initiated | 2024-07-24 |
| Classified | 2024-08-29 |
| Reported by FDA | 2024-09-04 |
| Distributed | Nationwide (US) |
| Quantity | 24,693,200 eaches |
| UPC / GTIN / UDI-DI | 30612479170316 |
| Model numbers | 102-S60C |
Product
McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)
Reason for recall
Affected syringes lack FDA clearance.
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-2940-2024. 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.