Symmetry Classic Plus® 36-1007Recalls & reported problems
Aspen Surgical Products, Inc. · Classic Plus® Needle Holder, Micro, w/Catch, 8 1/2 in; 212 mm · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887482009574), received between Aug 14, 2020 and Jun 2, 2026 — classified as 1 injury, 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Device Fell1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 2, 2026Break
COMPLAINANT ALLEGES "PURCHASED IN (B)(6) 2023 ONE OF THE JAWS HAS SNAPPED OFF - SENT TO THEIR OWN INSTRUMENT REPAIRER FOR ASSESSMENT AND CANT BE REPAIRED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25363876 ↗InjuryAug 14, 2020Device Fell
DURING A CAROTID SURGERY THE INSERTS OF THE NEEDLE HOLDER FELL OFF AND INTO THE PATIENT. THE PIECE WAS RETRIEVED WITH NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10411385 ↗
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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 13, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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