FDA Device recall Z-2365-2015
Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209
- FDA Device
- Class II
- terminated
- Published 2015-08-19
On 2015-08-19 the FDA classified a Class II recall of Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209 by Cadence, citing graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2365-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-09 |
| Published | 2015-08-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Cadence |
| Distribution | US |
Product
Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209
Reason
Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
Identifiers
| code_info | Packged Lots: Catalog Number 5208: 79895-01, 80044-02, 82350-01, W006510/1; Catalog Number 5209: 71880-01, 76434-…Packged Lots: Catalog Number 5208: 79895-01, 80044-02, 82350-01, W006510/1; Catalog Number 5209: 71880-01, 76434-01, 76461-01, 76461-02, 76461-03, 76461-04, 76461-05, 76461-06, 76461-07, 76461-08, 79748-01, 80044-03, W001711/1, W002337/1, W002886/1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2365-2015%22
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