Dusseldorf, N/A, Germany
Hager & Meisinger Gmbh recalls
2 recalls recorded since 2018, most recently on 15 July 2020. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)1
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 15 July 2020
- Terminated
- 24 February 2022
- Reason
- US-dates between the product package label and the bar code display.
- Distribution
- US Nationwide distribution including in the states of AZ, CA, FL, IN, NY, PA and TX.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2937-2020
- 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,
Ongoing Class II Medical devices
- Recall started
- 7 November 2018
- Reason
- Incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade packaging.
- Distribution
- US: NV, PA, FL, SC, IA, NC-
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0493-2020
- 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:
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.