Singles carbides by Meisinger — Class II medical device recall Z-0493-2020
Ongoing recall by Hager & Meisinger Gmbh, reported 2019-11-27, distributed in FL, IA, NC, NV, PA, SC. Incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade p
| Recall number | Z-0493-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hager & Meisinger Gmbh, Dusseldorf, N/A, Germany |
| Recall initiated | 2018-11-07 |
| Classified | 2019-11-19 |
| Reported by FDA | 2019-11-27 |
| Distributed | FL, IA, NC, NV, PA, SC |
| Quantity | 2,500 burs |
| Lot numbers | R23891 |
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:
Reason for recall
Incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade packaging.
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-0493-2020. 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.