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 | Terminated |
| Reason | US-dates between the product package label and the bar code display. |
| Product | SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage: Cutting of hard structures in the mouth, such as teeth or bone, it is also intended to cut hard metals, plastics, porcelains, and similar materials intended for use in the fabrication of dental devices. |
| Quantity | 144 units |
| Distribution | US Nationwide distribution including in the states of AZ, CA, FL, IN, NY, PA and TX. |
| Initiated | 2020-07-15 |
| Classified | 2020-09-04 |
| Terminated | 2022-02-24 |
| Recall number | Z-2937-2020 |
| 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-2937-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/86147/
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