Recall- Software error may not reflect alignment axis and incision position

Company: Oculus Optikgeraete GMBH
Date of Enforcement Report: 9/1/2022
Class II

PRODUCT

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

Recall Number:

Z-1672-2022

REASON

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

RECALLING FIRM/MANUFACTURER

Oculus Optikgeraete GMBH; Voluntary. Firm initiated.

VOLUME OF PRODUCT IN COMMERCE

21 systems with affected software

DISTRIBUTION

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

About the author

Allison joined SoftwareCPR in 2022, bringing along over ten years of passion for building teamwork and growth in organizations. This is established in part by the greatest University the South has to offer- Mississippi State.

SoftwareCPR Training Courses:

IEC 62304 and other Emerging Standards Impacting Medical Device Software

Being Agile & Yet Compliant

ISO 14971 SaMD Risk Management

Software Risk Management

Medical Device Cybersecurity

Software Verification

IEC 62366 Usability Process and Documentation

Or just email training@softwarecpr.com for more info.

Corporate Office

15148 Springview St.
Tampa, FL 33624
USA
+1-781-721-2921
Partners located in the US (CA, FL, MA, MN, TX) and Canada.