Vector TAS Modular Driver — Class II medical device recall Z-0205-2013
Terminated recall by Ormco/Sybronendo, reported 2012-11-14, distributed nationwide. The Instructions For Use (IFUs) for Vector TAS Modular Driver for some foreign language sections incorrectly l
| Recall number | Z-0205-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ormco/Sybronendo, Glendora, CA, United States |
| Recall initiated | 2011-12-12 |
| Classified | 2012-11-05 |
| Reported by FDA | 2012-11-14 |
| Terminated | 2012-11-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, BG, CA, CH, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LU, NL, PL, RO, RS, SI, TR |
| Quantity | 4,543 |
| Model numbers | 601-0007, 601-0010 |
Product
Vector TAS Modular Driver, a manual driver for Vector TAS dental screws.
Reason for recall
The Instructions For Use (IFUs) for Vector TAS Modular Driver for some foreign language sections incorrectly lists the sterilization temperature as 130¿C. The correct sterilization temperature should be listed as 132¿C and/or 270¿F.
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-0205-2013. 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.