FDA Device recall Z-0493-2020
Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round end
- FDA Device
- Class II
- ongoing
- Published 2019-11-27
On 2019-11-27 the FDA classified a Class II recall of Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round end by Hager And Meisinger, citing incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0493-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-11-07 |
| Published | 2019-11-27 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Hager And Meisinger |
| Distribution | FL, IA, NC, NV, PA, SC |
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
Incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade packaging.
Identifiers
| code_info | Lot #R23891 UDI: +E0HM26UN2453140099/$$8250523R23891+ |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0493-2020%22
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