Horizon 6FA Centrifuge, RegenLab, Swiss 00-276-088-001Recalls & reported problems

Drucker Diagnostics · General purpose laboratory centrifuge for sample separation. · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 1
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810052862293), received between Apr 5, 2024 and Apr 5, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Unintended Electrical Shock” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Unintended Electrical Shock1

Patient problems

Electric Shock1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

InjuryApr 5, 2024Unintended Electrical Shock; Unintended Electrical Shock
NURSE ELECTRIFIED, BURNED ON THE ARM AND HOSPITALIZED, IN A WORK STOPPAGE. NO ADDITIONAL INFORMATION HAS BEEN PROVIDED BY THE CUSTOMER OR THE INJURED PARTY AT THIS TIME.
Patient problems: Electric Shock
MAUDE report 19054017 ↗

Device details

UDI-DI	`00810052862293`
Brand	Horizon 6FA Centrifuge, RegenLab, Swiss
Model	00-276-088-001
Company	Drucker Diagnostics
Product code	JQC · Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	—
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jun 10, 2022

Device type (GMDN): General-purpose centrifuge IVD

An electrically-powered device intended to be used to separate the components of multiple types and various volumes of clinical suspensions using centrifugal force. It is a self-contained unit with an electric motor, a vertical shaft, and a horizontal rotor attached to the upper end. It is typically used to centrifuge various types of clinical specimens, either alone or after addition of reagents or other additives, for subsequent in vitro diagnostic analysis. It may additionally have refrigeration capabilities to perform temperature-sensitive procedures.

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Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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