Arthrex® AR-1340TRecalls & reported problems
Arthrex, Inc. · PEEKPOWER HTO PLATE BONE SPREADER · 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 00888867012295), received between May 1, 2025 and May 1, 2025 — 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionMay 1, 2025Break; Break
ON 04/10/2025, A SALES REPRESENTATIVE REPORTED VIA SEMS-(B)(4) THAT AN AR-1340T PEEKPOWER HTO PLATE BONE SPREADERS TIP BROKE. THIS OCCURRED DURING A CASE. THE FRAGMENT WAS RETRIEVED, AND NOTHING WAS LEFT INSIDE THE PATIENT. THEY REPLACED THE DEVICE WITH A SIMILAR PRODUCT TO COMPLETE THE CASE SUCCESSFULLY. THE ITEM WILL BE RETURNED TO ARTHREX FOR EVALUATION. THERE WAS NO PATIENT HARM OR ADVERSE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21942538 ↗
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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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