FDA Device recall Z-0635-2018
OCULUS Pentacam AXL, Model 70100, software versions 1.21r01, 1.21r03, 1.21r11, and 1.21r13
- FDA Device
- Class II
- terminated
- Published 2018-02-28
On 2018-02-28 the FDA classified a Class II recall of OCULUS Pentacam AXL, Model 70100, software versions 1.21r01, 1.21r03, 1.21r11, and 1.21r13 by Oculus Optikgeraete, citing the device software versions have an anomaly which may produce an erroneous marking for the quality specification value.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0635-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-11-21 |
| Published | 2018-02-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Oculus Optikgeraete |
| Distribution | CA, FL |
Product
OCULUS Pentacam AXL, Model 70100, software versions 1.21r01, 1.21r03, 1.21r11, and 1.21r13. The firm name on the label is OCULUS Optikgerate GmbH, Made in Germany. The Pentacam AXL is designed to take photos of the anterior segment of the eye, which includes the cornea, pupil, anterior chamber, and lens of the eye, to evaluate corneal shape, analyze condition of the lens (opaque crystalline lens), analyze the anterior chamber angle, analyze anterior chamber depth, analyze the volume of the anterior chamber, analyze anterior or posterior cortical opacity, analyze the location of cataracts (nuclear, sub capsular and/or cortical), using cross slit imaging with densitometry, corneal thickness, axial length, and white-to-white distance. The Pentacam AXL also performs calculations to assist physicians in determining the power of the intraocular lens for implantation.
Reason
The device software versions have an anomaly which may produce an erroneous marking for the quality specification value
Identifiers
| code_info | Serial numbers: 70100 0021 6190, 70100 0301 5170, 70100 0311 6150, 70100 0331 7130, 70100 0401 5101, 70100 0421 6101…Serial numbers: 70100 0021 6190, 70100 0301 5170, 70100 0311 6150, 70100 0331 7130, 70100 0401 5101, 70100 0421 6101, 70100 0641 7170, 70100 0831 7150, 70100 1021 6190, 70100 1101 5170, 70100 1541 7170, 70100 1631 7140, 70100 1731 7140, 70100 1831 7150, 70100 1901 6130, 70100 2211 6150, 70100 2221 6190, 70100 2231 7130, 70100 2241 7160, 70100 2511 6170, 70100 2641 7170, 70100 2731 7140, 70100 2801 6130, 70100 2821 7110, 70100 2931 7150, 70100 3221 6190, 70100 3701 6110, 70100 3731 7140, 70100 3931 7150, 70100 4041 7160, 70100 4211 6150, 70100 4231 7130, 70100 4401 5121, 70100 4511 6170, 70100 4711 6170, 70100 4831 7150, 70100 4931 7150, 70100 5311 6160, 70100 5531 7140, 70100 5611 6170, 70100 5621 6111, 70100 5831 7150, 70100 5931 7150, 70100 6101 5170, 70100 6221 6101, 70100 6231 7130, 70100 6331 7130, 70100 6401 5121, 70100 6421 6101, 70100 6631 7140, 70100 6801 6130, 70100 6811 6190, 70100 6821 7110, 70100 7041 7160, 70100 7221 6101, 70100 7401 5121, 70100 7511 6170, 70100 7531 7 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0635-2018%22
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