MEDLINE LUER SLIP DISPOSABLE SYRINGE WITHOUT NEEDLE — Class II medical device recall Z-1938-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-06-12, distributed nationwide. It has been identified that testing documentation does not support that the syringes can successfully deliver
| Recall number | Z-1938-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-04-22 |
| Classified | 2024-05-31 |
| Reported by FDA | 2024-06-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA, PA |
| Quantity | 5,075,234 syringes |
| UPC / GTIN / UDI-DI | 10080196306183 |
| Model numbers | YR101020 |
Product
MEDLINE LUER SLIP DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101020
Reason for recall
It has been identified that testing documentation does not support that the syringes can successfully deliver accurate volumes across the full range of their claimed graduated capacity and may pose a risk to patient health.
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-1938-2024. 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.