Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany Pentacam HR REF 70900. Used to image the anterior segment of the eye. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pentacam HR REF 70900. Used to image the anterior segment of the eye.
Brand
Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Software version: 1.26r26 and 1.26r27 Model Number: 70900 UDI-DI Code: 04049584000026 Serial Numbers: 70900 0574 8160 70900 0925 0240 70900 0995 2250 70900 1664 8130 70900 1995 2250 70900 3451 7060 70900 3795 2250 70900 3965 1270 70900 4041 7010 70900 4172 2110 70900 4795 2250 70900 6234 7150 70900 7552 1160 70900 7952 1180 70900 8804 6140 70900 8813 3140 70900 9142 0121 70900 9695 2250 70900 9795 2250
Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany is recalling Pentacam HR REF 70900. Used to image the anterior segment of the eye. due to Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs
Recommended Action
Per FDA guidance
On 07/08/2022, OCULUS GmbH issued an "Urgent safety information Corrective Action " Letter to its subsidiary OCULUS Inc via UPS express which identifies a software error in the software version 1.26r26 and 1.26r27 in the IOL calculator of the Pentacam software. Corrective measures to be taken: A software update to version 1.26r28 must be performed on all computers used and affected in connection with the Pentacam and additional workstations. Users should refrain from using the printout of the IOL calculator for affected installations until after the software update has been carried out. For questions or support - contact OCULUS Inc Service Team at 425-670-9977 or email service@oculususa.com or fsca@oculus.de
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CO, CT, FL, GA, HI, ID, IL, IA, KS, KY, ME, MD, MI, MN, MS, MO, NE, NH, NJ, NM, NY, NC, OH, PA, SC, SD, TN, TX, UT, VA, WA, WI, WY, PR
Page updated: Jan 10, 2026