Medical DeviceSep 16, 2020
Hager & Meisinger Gmbh SINGLES Carbide US-No recall — FDA Z-2937-2020
US-dates between the product package label and the bar code display.
Class IIFDA: TerminatedHager & Meisinger Gmbh
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceNov 27, 2019
Hager & Meisinger Gmbh Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round recall — FDA Z-0493-2020
Incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade packaging.
Class IIFDA: OngoingHager & Meisinger Gmbh
Understanding this recall history
This page summarizes recall records in which the official source identifies Hager & Meisinger Gmbh as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.