FDA Device recall Z-0030-2017
Zenostar MT Color C1 60ml, art. no. 681059
- FDA Device
- Class II
- terminated
- Published 2016-10-12
On 2016-10-12 the FDA classified a Class II recall of Zenostar MT Color C1 60ml, art. no. 681059 by Ivoclar Vivadent, citing the primary packaging of these products may show leaks in individual cases. As a consequence, the liquid may escape inadvertently and direct contact with this liquid may lead to s….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0030-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-05-27 |
| Published | 2016-10-12 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ivoclar Vivadent |
| Distribution | US |
Product
Zenostar MT Color C1 60ml, art. no. 681059. Product Usage: For coloring dental porcelain
Reason
The primary packaging of these products may show leaks in individual cases. As a consequence, the liquid may escape inadvertently and direct contact with this liquid may lead to skin irritation.
Identifiers
| code_info | Lot No: U51611, exp date: Nov 11 2017; U50758, exp date: Nov 5 2017; U43929, exp date: Nov 5 2017; and U38834, exp date: Sep 16 2017 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0030-2017%22
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