FORCE FIBER IPN000852 (REF 3910-900-020)Recalls & reported problems
Teleflex Incorporated · Force Fiber White/Blue Co-Braid Size 2 38" HC-5 Needle Stryker · Class 2 · Implant
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 04026704603398), received between Mar 18, 2023 and Mar 18, 2023 — 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.
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.
MalfunctionMar 18, 2023Break; Break
REPORTED ISSUE: SUTURE BURST WITH TRACTION CAUSING PROBLEM IN SURGERY. ADDITIONAL INFORMATION: THE DISTRIBUTOR STATED THAT THE PROCEDURE WAS DELAYED AND ULTIMATELY THE PATIENT'S PATHOLOGY COULD NOT BE COMPLETELY RESOLVED. A RECONSTRUCTION OF THE ANTERIOR CRUCIATE LIGAMENT AND SUTURE OF THE MENISCAL ROOT WAS BEING PERFORMED BY ARTHROSCOPY. THE DELAY WAS BECAUSE AN ATTEMPT WAS MADE TO SEEK AUTHORIZATION FROM THE HEALTH AUTHORITY TO USE THE MATERIAL OF ANOTHER MANUFACTURER. THE PATIENT WAS UNDER SPINAL ANESTHESIA THROUGHOUT THE ENTIRE PROCEDURE. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16569442 ↗
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- Arthrex® AR-4501Arthrex, Inc. · SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE403 reports
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- LUPINE ORTHOCORD 210712Medos International Sàrl · SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE357 reports
- FAST-FIX 72201494Smith & Nephew, Inc. · SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE249 reports
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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