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PROLENE EP8714HRecalls & reported problems

Ethicon, LLC · Blue Monofilament (Polypropylene), Nonabsorbable Surgical Suture · Class 2 · Implant

All models of PROLENE (358)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705031231245), received between Dec 27, 2018 and Jan 24, 2023 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (2 reports).

21 other recalls cover devices cleared under the same FDA submission (K133356); they may or may not involve this specific model.

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

  • Break2

Patient problems

  • Foreign Body In Patient1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 24, 2023Break; Break

    IT WAS REPORTED THAT A PATIENT UNDERWENT AN UNKNOWN PROCEDURE ON AN UNKNOWN DATE AND SUTURE WAS USED. THE PATIENT HAS A RETAINED NEEDLE IN THE ABDOMEN. ADDITIONAL INFORMATION WAS REQUESTED.

    Patient problems: Foreign Body In Patient

    MAUDE report 16233491 ↗
  • MalfunctionDec 27, 2018Break; Break

    IT WAS REPORTED THAT A PATIENT UNDERWENT A PANCREATICODUODENECTOMY PROCEDURE ON (B)(6) 2018 AND A SUTURE WAS USED. DURING SURGERY, IT WAS FOUND THAT THE NEEDLE TIP HAD BEEN MISSING BEFORE USE. UPON EVALUATION OF THE RETURNED SAMPLE, A FRACTURE WAS OBSERVED AT THE TIP OF THE NEEDLE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8201224 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K133356. One submission often covers many models, so check the product and lot details in each record.

  • Z-1515-2025 · Mar 7, 2025 · Open, Classified
    PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM
  • Z-1096-2025 · Dec 20, 2024 · Open, Classified
    PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general soft tissue approximation and/or ligation, including use in ca
  • Z-2458-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE 24"(60CM) 7-0 BLUE, D8881
  • Z-2466-2018 · May 7, 2018 · Terminated
    PRONOVA SUTURE BLUE 122CM M1.5, D10189
  • Z-2455-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE 30"(75CM) 8-0 BLUE, D8292
  • Z-2461-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE BLUE 48" 4-0 D/A SH-1, D9746
  • Z-2460-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE 4"(10CM) 8-0 BLUE, D9662
  • Z-2452-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE 30"(75CM) 4-0 BLUE, D7748
  • Z-2459-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE 36"(90CM) 4-0 BLUE, D9067
  • Z-2465-2018 · May 7, 2018 · Terminated
    PRONOVA SUTURE BLUE MONO POLY - SH-1 Taperpoint 1/2C, D10027
  • Z-2450-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE 4-36"(90CM) 4-0 BLUE, D5988
  • Z-2448-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE MONO BLUE - BV1755 Taper Point 3/8C, D10031
  • Z-2462-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE 36"(90CM) 3-0 BLU, D9844
  • Z-2457-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE 24"(60CM) 6-0 BLUE, D8688
  • Z-2463-2018 · May 7, 2018 · Terminated
    PROLENE SUTURE MONO BLUE BV1755 Taperpoint 3/8C, D9995

…and 6 more.

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Sources and updates

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