FDA recall record

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 IIclassification
Z-0493-2020official record ID
Nov 27, 2019report date

Recall record at a glance

Official recordZ-0493-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmHager & Meisinger Gmbh
Report dateNov 27, 2019
Recall initiation dateNov 7, 2018
Quantity2500 burs
LocationDusseldorf, N/A, Germany

Official product description

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:

Why the product was recalled

Incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade packaging.

Distribution information

US: NV, PA, FL, SC, IA, NC-

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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