Micro-Mate Tuberculin Glass Syringe — Class II medical device recall Z-2365-2015
Terminated recall by Cadence Inc., reported 2015-08-19, distributed nationwide. Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
| Recall number | Z-2365-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cadence Inc., Cranston, RI, United States |
| Recall initiated | 2015-07-09 |
| Classified | 2015-08-10 |
| Reported by FDA | 2015-08-19 |
| Terminated | 2016-07-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, DK, IT |
| Quantity | 1,665 units |
| Model numbers | 5208, 5209, 71880-01, 76434-01, 76461-01, 76461-02, 76461-03, 76461-04, 76461-05, 76461-06, 76461-07, 76461-08, 79748-01, 79895-01, 80044-02, 80044-03, 82350-01, W001711/1, W002337/1, W002886/1, W006510/1 |
Product
Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209
Reason for recall
Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
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-2365-2015. 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.