FDA Device recall Z-2364-2015
Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212
- FDA Device
- Class II
- terminated
- Published 2015-08-19
On 2015-08-19 the FDA classified a Class II recall of Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212 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-2364-2015 |
| 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
Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212
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 5202: 79713-04, 80468-05, W003542/1, W006324/1, W006324/2, W006324/3, W006324/4, W00632…Packged Lots: Catalog Number 5202: 79713-04, 80468-05, W003542/1, W006324/1, W006324/2, W006324/3, W006324/4, W006324/5; Catalog Number 5205: 79748-03; Catalog Number 5212: W008136/1, W008686/1, W011240/1, W010905/1, W012135/1, W014053/1, W015838/1, W011240 |
|---|
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-2364-2015%22
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