2de14 3-0 Pdo 24 X 24 RA-1052QRecalls & reported problems
Surgical Specialties México, S. de R.L. de C.V. · 2de14 3-0 Pdo 24 X 24 · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00848782019021), received between Nov 17, 2023 and Nov 17, 2023 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Impaired Healing1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 17, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE REPORTER MENTIONED THAT THE HOSPITAL CLINICAL FEEDBACK FROM (B)(6) THIS YEAR BEGAN TO USE RA-1052Q BATCH NUMBER AAIB752, (B)(4) OF THE PATIENTS HAVE AN INCISION INFECTION AFTER SUTURING, THE HOSPITAL SIDE HOPED WE CAN PROVIDE THE REPORT TO THE HOSPITAL. I HAVE CHECKED THE ADRS SYSTEM AND FOUND THIS CASE HAS NOT BEEN REPORTED. BASED ON LIMITED COMPLAINT INFORMATION, THE END USER PERFORMED ORTHOPEDIC SURGERY, NO VIDEO OR PHOTOS PROVIDED. NO CULTURES OR RESULTS PROVIDED. THE EXACT TYPE OF INFECTION NOT IDENTIFIED. BY CONTACTING WITH THE REPORTER AND THE HOSPITAL, THEY CAN PROVIDE AN UNOPENED SUTURE FOR INVESTIGATION.
Patient problems: Impaired Healing
MAUDE report 18157062 ↗
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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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