RecallRadar

FDA Device recall Z-1672-2022

Pentacam AXL Wave REF 70020

On 2022-09-07 the FDA classified a Class II recall of Pentacam AXL Wave REF 70020 by Oculus Optikgeraete, citing due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1672-2022
ClassificationClass II
Statusongoing
Initiated2022-07-08
Published2022-09-07
Last updated2026-09-13 11:56 UTC
CompanyOculus Optikgeraete
DistributionAL, AR, AZ, CO, CT, FL, GA, HI, IA, ID, IL, KS, KY, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, PA, PR, SC, SD, TN, TX, UT, VA, WA, WI, WY

Product

Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.

Reason

Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs

Identifiers

code_info
Software version: 1.26r26 and 1.26r27 Model Number: 70020 UDI-DI Code: 04049584025357 Serial Numbers: 70020 0111 0201…Software version: 1.26r26 and 1.26r27 Model Number: 70020 UDI-DI Code: 04049584025357 Serial Numbers: 70020 0111 0201 70020 0211 0201 70020 0311 0211 70020 0711 1230 70020 1211 0201 70020 1321 1211 70020 2411 0211 70020 2911 1250 70020 3511 0211 70020 3801 0230 70020 4701 0210 70020 4811 1250 70020 5411 0211 70020 5701 0210 70020 6611 1230 70020 6621 1211 70020 7011 0201 70020 7511 1230 70020 8021 1290 70020 8701 0210 70020 9011 0201

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1672-2022%22

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