bluephase style Light probe Pin-point 6>2 mm black REF # 636 241 — Class II medical device recall Z-1740-2014
Terminated recall by Ivoclar Vivadent, Inc., reported 2014-06-18, distributed nationwide. A stock check revealed broken glass fibers between the connector and the fiber bundle in a large number of the
| Recall number | Z-1740-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ivoclar Vivadent, Inc., Buffalo, NY, United States |
| Recall initiated | 2014-04-14 |
| Classified | 2014-06-09 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2015-11-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 241 units |
| Reason classes | foreign material |
| Model numbers | 241, 636 |
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 for recall
A stock check revealed broken glass fibers between the connector and the fiber bundle in a large number of these light probes.
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-1740-2014. 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.