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Recall Observatory FDA recall evidence

Device product

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

Z-1672-2022

July 08, 2022

Class II

Product summary

Firm
Oculus Optikgeraete GMBH
Event
Event 90661
Status
Ongoing
Classification
Class II
Quantity
21 systems with affected software
Official record key
device-enforcement:Z-1672-2022

Official wording

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

Code information: 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

Distribution pattern: U.S.: AL, AR, AZ, CAQ, CO, CT, FL, GA, HI, IA, ID, IL, KS, KY, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, PA, Puerto Rico, SC, SD, TN, TX, UT, VA, WA, WI, and WY O.U.S.: N/A

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software issue