Ds24 3-0 Undbrpga-Fa 27"/70cm M442NRecalls & reported problems
Surgical Specialties México, S. de R.L. de C.V. · Ds24 3-0 Undbrpga-Fa 27"/70cm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00848782017515), received between Oct 27, 2022 and Aug 14, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Detachment of Device or Device Component1
- Separation Problem1
Patient problems
- Nodule1
- Pain1
- Post Operative Wound Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 14, 2024Detachment of Device or Device Component; Separation Problem; Detachment of Device or Device Component; Separation Problem
PER THE REPORTER THERE WAS AN ISSUE WITH ABSORPTION OF THE SUTURES. THE ISSUE OCCURRED POST-OPERATIVELY. THE SUTURE STUMP WAS REMOVED FROM THE WOUND TO RESOLVE THE ISSUE.
Patient problems: Nodule
MAUDE report 19983785 ↗InjuryOct 27, 2022Adverse Event Without Identified Device or Use Problem
WOUND HEALING DIFFICULTY, REPORT#(B)(4) ADRS 9/15/2022 UPDATED 10/14/2022 ON 19 AUG 2022, THE PATIENT DELIVERED A BOY BY CAESAREAN SECTION DUE TO "CEPHALOPELVIC DISPROPORTION AND PREMATURE RUPTURE OF MEMBRANES", WITH ABSORBABLE SURGICAL SUTURE M442N (3-0). THE ABDOMINAL INCISION WAS FOUND LIQUID LEAKED AND PRESSURED PAIN ON (B)(6), THEN WAS TREATED WITH ESCALATING ANTIBIOTICS. ONE WEEK LATER, THE ABDOMINAL INCISION WAS SEEN TO BE HEALING.
Patient problems: Pain; Post Operative Wound Infection
MAUDE report 15678168 ↗
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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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