FDA Device recall Z-2937-2020
SINGLES Carbide US-No. FG556
- FDA Device
- Class II
- terminated
- Published 2020-09-16
On 2020-09-16 the FDA classified a Class II recall of SINGLES Carbide US-No. FG556 by Hager And Meisinger, citing US-dates between the product package label and the bar code display.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2937-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-07-15 |
| Published | 2020-09-16 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Hager And Meisinger |
| Distribution | US |
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.
Reason
US-dates between the product package label and the bar code display.
Identifiers
| code_info | LOT R50753 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2937-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.