NA 690.380Recalls & reported problems
Synthes GmbH · GRAPHIC CASE FOR 7.3MM CANNULATED SCREW SET · Class 1
Data updated Oct 16, 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 10886982253224), received between Jun 26, 2023 and Jun 26, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Illegible Information” (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.
Most reported problems
Device problems
- Illegible Information1
- Incorrect Measurement1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 26, 2023Incorrect Measurement; Mechanical Problem; Illegible Information; Incorrect Measurement; Mechanical Problem; Illegible Information
IT WAS REPORTED THAT ON AN UNKNOWN DATE, THERE WAS AN OLD CANNULATED SCREW SET THAT NO LONGER FUNCTIONED. THE PRODUCT NUMBERS HAD FADED, AND IT WAS DIFFICULT TO MEASURE THE SCREW LENGTHS. THIS REPORT INVOLVES ONE GRAPHIC CASE FOR 7.3MM CANNULATED SCREW SET. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17198281 ↗
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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 16, 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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