Symmetry Olsen 607000Recalls & reported problems
Aspen Surgical Products, Inc. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841785107702), received between Jan 29, 2021 and Jan 29, 2021 — classified as 1 malfunction.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 29, 2021Adverse Event Without Identified Device or Use Problem
THE PATIENT EXPERIENCED A SOFT TISSUE INJURY AFTER REMOVAL OF THE EYE SHIELD. THERE WAS NO LONG TERN AFFECT ON THE PATIENT.
Patient problems: Unspecified Tissue Injury
MAUDE report 11251234 ↗
Other Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) devices
- CARDINAL HEALTH CAHEYEWEARCardinal Health 200, LLC · Shield, eye, ophthalmic (including sunlamp protective eyewear and post-mydriatic eyewear)2 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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