2t9 #1 Pdo 24 X 24 RA-1031QRecalls & reported problems
Surgical Specialties México, S. de R.L. de C.V. · 2t9 #1 Pdo 24 X 24 · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00848782018833), received between Dec 2, 2024 and Feb 21, 2025 — classified as 3 injuries.
The most frequently reported specific device problem is “Separation Problem” (3 reports).
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.
Reports received per month
Most reported problems
Device problems
- Separation Problem3
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryFeb 21, 2025Detachment of Device or Device Component; Separation Problem; Detachment of Device or Device Component; Separation Problem
IT WAS REPORTED ON (B)(6) 2025 THAT A NEEDLE DETACHED FROM A SUTURE INTRAOPERATIVELY. NO PATIENT INJURY OCCURRED; HOWEVER, MEDICAL INTERVENTION WAS REQUIRED TO RETRIEVE THE NEEDLE FROM THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21439783 ↗InjuryDec 2, 2024Separation Problem; Separation Problem
IT WAS REPORTED ON 7 NOV 2024 THAT TWO NEEDLES DETACHED FROM THE SUTURES INTRAOPERATIVELY. NO PATIENT INJURY OCCURRED; HOWEVER, INTERVENTION WAS REQUIRED TO RETRIEVE THE NEEDLES FROM THE PATIENT. THIS REPORT SERVES AS THE SECOND OF TWO REPORTS. REF: 3010692967-2024-00099.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20818770 ↗InjuryDec 2, 2024Separation Problem; Separation Problem
IT WAS REPORTED ON (B)(6) 2024 THAT TWO NEEDLES DETACHED FROM THE SUTURES INTRAOPERATIVELY. NO PATIENT INJURY OCCURRED; HOWEVER, INTERVENTION WAS REQUIRED TO RETRIEVE THE NEEDLES FROM THE PATIENT. THIS REPORT SERVES AS THE FIRST OF TWO REPORTS. REF: 3010692967-2024-00100.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20818731 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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