Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 78606

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
November 21, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Oculus Optikgeraete GMBH

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

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.

Z-0635-2018
Recall number
Z-0635-2018
Initiated
November 21, 2017
Classification
Class II
Status
Terminated
Recalling firm
Oculus Optikgeraete GMBH
Quantity
83 devices

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software versions have an anomaly

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The device software versions have an anomaly which may produce an erroneous marking for the quality specification value

Code information

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 7140, 70100 7631 7140, 70100 7731 7150, 70100 7831 7150, 70100 7931 7150, 70100 8121 6190, 70100 8141 7160, 70100 8511 6170, 70100 8531 7140, 70100 8611 6170, 70100 8631 7140, 70100 8721 7110, 70100 8731 7150, 70100 9041 7160, 70100 9221 6101, 70100 9231 7130, 70100 9301 5101, 70100 9411 6160, 70100 9521 6111, 70100 9711 6190, 70100 9731 7150, 70100 9911 6190, 70100 9931 7150, 70100 7411 6160, 70100 8021 6190, and 70100 4531 7140.

Distribution pattern

US Distribution to the states of : CA and FL. There were no foreign/military/government accounts.

Field note

Send feedback

We'll only use this to respond to your feedback.