FDA Device recall Z-1740-2014
bluephase style Light probe Pin-point 6>2 mm black REF # 636 241
- FDA Device
- Class II
- terminated
- Published 2014-06-18
On 2014-06-18 the FDA classified a Class II recall of bluephase style Light probe Pin-point 6>2 mm black REF # 636 241 by Ivoclar Vivadent, citing A stock check revealed broken glass fibers between the connector and the fiber bundle in a large number of these light probes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1740-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-14 |
| Published | 2014-06-18 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ivoclar Vivadent |
| Distribution | US |
Product
bluephase style Light probe Pin-point 6>2 mm black REF # 636 241. The accessory is a pin point light probe, an accessory to a dental curing light Ultraviolet activator for polymerization for use during dental curing.
Reason
A stock check revealed broken glass fibers between the connector and the fiber bundle in a large number of these light probes.
Identifiers
| code_info | Reference number 636241, all lots |
|---|
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-1740-2014%22
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