RecallRadar

FDA Device recall Z-0614-2021

Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the objective refractive values…

On 2020-12-23 the FDA classified a Class II recall of Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the objective refractive values… by Carl Zeiss Meditec Ag, citing due to the incorrect DC/DC converter being assembled onto the communication board. As a result the effectiveness of the communication board cannot be guaranteed in that the safety….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0614-2021
ClassificationClass II
Statusterminated
Initiated2020-08-06
Published2020-12-23
Last updated2026-09-13 11:55 UTC
CompanyCarl Zeiss Meditec Ag
DistributionUS

Product

Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the objective refractive values and keratometric characteristics of the human eye. The results are used to assist the process of prescribing optical aids such as eyeglasses and contact lenses.

Reason

Due to the incorrect DC/DC converter being assembled onto the communication board. As a result the effectiveness of the communication board cannot be guaranteed in that the safety function of the board would be insufficient resulting in an increased leakage of current and potentially cause electrical shocks to the user.

Identifiers

code_infoModel: VISUREF 150 Catalog Number: 000000-2227-967 Serial Numbers: Pending

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-0614-2021%22

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