Class II — Hager & Meisinger Gmbh
| Recalling firm | HAGER & MEISINGER GMBH |
|---|---|
| Registered facility | HAGER & MEISINGER GMBH (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade packaging. |
| Product | Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round end; US-No 245; Reference: HMUN245-009; Shank: FG/314; Head Size 1/10mm: 009,Head Length/mm: |
| Quantity | 2500 burs |
| Distribution | US: NV, PA, FL, SC, IA, NC- |
| Initiated | 2018-11-07 |
| Classified | 2019-11-19 |
| Recall number | Z-0493-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Hager & Meisinger Gmbh (Z-0493-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83776/
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