Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with… — Class II medical device recall Z-0623-2014
Terminated recall by Aesculap, Inc., reported 2014-01-15, distributed in NY, PA, TN, TX. Certain lots of the Aesculap Hi Line XXS handpiece (part # GB790R) were recalled due to a possible failure of
| Recall number | Z-0623-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap, Inc., Center Valley, PA, United States |
| Recall initiated | 2013-12-09 |
| Classified | 2014-01-03 |
| Reported by FDA | 2014-01-15 |
| Terminated | 2014-12-02 |
| Distributed | NY, PA, TN, TX |
| Countries outside the US | AT, CH, DE, DK, ES, FI, FR, HK, IL, IT, JP, NL, PL, TW |
| Quantity | 14 |
| Lot numbers | 4504300008, 4504328565, 4504385018, 4504685847, 4804685865 |
| Model numbers | GB790R |
Product
Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with the HiLAN¿ and microspeed motor systems to hold burrs which cut and shape bone.
Reason for recall
Certain lots of the Aesculap Hi Line XXS handpiece (part # GB790R) were recalled due to a possible failure of the handpiece.
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-0623-2014. 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.