Symmetry Surgical GARRETT 55-7003Recalls & reported problems
Aspen Surgical Products, Inc. · Symmetry® Dilator; Garrett; 1 mm Tip; Malleable; 5 1/2 in; 139 mm · Class 2
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 00887482085240), received between Jun 13, 2019 and Jun 13, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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
- Break1
- Detachment of Device or Device Component1
- Material Twisted/Bent1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 13, 2019Break; Detachment of Device or Device Component; Material Twisted/Bent
DURING A PROCEDURE, THE TIP OF THE DILATOR BROKE OFF WHILE IT WAS BEING BENT INTO SHAPE FOR USE. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8696320 ↗
Other Dilator, Vessel, Surgical devices
- Vascular Probe 7451015Synovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7151015Synovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7451015ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7152025Synovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7452025ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7081520Synovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7081520ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7151015ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 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.
How reports and recalls are matched · Editorial policy · Report an error on this page