MERSILENE 1764GRecalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10705031002463), received between Dec 23, 2019 and Dec 23, 2019 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (7 reports).

8 other recalls cover devices cleared under the same FDA submission (K946173); 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

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 23, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THERE WAS AN ERROR IN SUTURE PACKAGING. IT WAS REPORTED THAT THE BOXES WERE INCORRECTLY PRINTED, SINCE THE CODE HAD THE WRONG NEEDLE. THE SUTURE IS SUPPOSED TO HAVE S-24 NEEDLE, HOWEVER THE PACKAGE SAYS S14. THE ISSUE WAS NOTICED IN A WAREHOUSE. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9512201 ↗
• MalfunctionDec 23, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THERE WAS AN ERROR IN SUTURE PACKAGING. IT WAS REPORTED THAT THE BOXES WERE INCORRECTLY PRINTED, SINCE THE CODE HAD THE WRONG NEEDLE. THE SUTURE IS SUPPOSED TO HAVE S-24 NEEDLE, HOWEVER THE PACKAGE SAYS S14. THE ISSUE WAS NOTICED IN A WAREHOUSE. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9512126 ↗
• MalfunctionDec 23, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THERE WAS AN ERROR IN SUTURE PACKAGING. IT WAS REPORTED THAT THE BOXES WERE INCORRECTLY PRINTED, SINCE THE CODE HAD THE WRONG NEEDLE. THE SUTURE IS SUPPOSED TO HAVE S-24 NEEDLE, HOWEVER THE PACKAGE SAYS S14. THE ISSUE WAS NOTICED IN A WAREHOUSE. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9512107 ↗
• MalfunctionDec 23, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THERE WAS AN ERROR IN SUTURE PACKAGING. IT WAS REPORTED THAT THE BOXES WERE INCORRECTLY PRINTED, SINCE THE CODE HAD THE WRONG NEEDLE. THE SUTURE IS SUPPOSED TO HAVE S-24 NEEDLE, HOWEVER THE PACKAGE SAYS S14. THE ISSUE WAS NOTICED IN A WAREHOUSE. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9511903 ↗
• MalfunctionDec 23, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THERE WAS AN ERROR IN SUTURE PACKAGING. IT WAS REPORTED THAT THE BOXES WERE INCORRECTLY PRINTED, SINCE THE CODE HAD THE WRONG NEEDLE. THE SUTURE IS SUPPOSED TO HAVE S-24 NEEDLE, HOWEVER THE PACKAGE SAYS S14. THE ISSUE WAS NOTICED IN A WAREHOUSE. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9511874 ↗
• MalfunctionDec 23, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THERE WAS AN ERROR IN SUTURE PACKAGING. IT WAS REPORTED THAT THE BOXES WERE INCORRECTLY PRINTED, SINCE THE CODE HAD THE WRONG NEEDLE. THE SUTURE IS SUPPOSED TO HAVE S-24 NEEDLE, HOWEVER THE PACKAGE SAYS S14. THE ISSUE WAS NOTICED IN A WAREHOUSE. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9511830 ↗
• MalfunctionDec 23, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THERE WAS AN ERROR IN SUTURE PACKAGING. IT WAS REPORTED THAT THE BOXES WERE INCORRECTLY PRINTED, SINCE THE CODE HAD THE WRONG NEEDLE. THE SUTURE IS SUPPOSED TO HAVE S-24 NEEDLE, HOWEVER THE PACKAGE SAYS S14. THE ISSUE WAS NOTICED IN A WAREHOUSE. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9511791 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K946173. One submission often covers many models, so check the product and lot details in each record.

• Z-1516-2025 · Mar 7, 2025 · Open, Classified
  ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH
• Z-1097-2025 · Dec 20, 2024 · Open, Classified
  PERMA-HAND Silk Suture, REF: K872H, W723H, 623H, K833H; Perma-hand Silk Suture is indicated for use in general soft tissue approximation and/or ligation, including use in cardiovas
• Z-2486-2020 · Jun 10, 2020 · Open, Classified
  PERMA-HAND/MERSILK SILK BLU and VIRGIN SILK BLU, Product Codes EH7457G EH7983G FV768 FV769 FV7771 U7058 U7059 W1782 W1784 W1819 W1820 W818 W819 W870
• Z-1841-2019 · Apr 19, 2019 · Terminated
  ETHIBOND EXCEL Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1 Product Code: X425H Product Usage: ETHIBOND EXCEL Suture is intended for use in general soft tissue app
• Z-1842-2019 · Apr 19, 2019 · Terminated
  ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX Product Code: X865W Product Usage: ETHIBOND EXCEL Suture is intended for use in general soft tissue appr
• Z-0747-2019 · Dec 18, 2018 · Terminated
  PERMA-HAND Silk Suture Size 5, Black 30" (75cm) Double Armed LR Needles, Product Code 485T Product Usage: PERMA-HAND* suture is indicated for use in general soft tissue approxima
• Z-1839-2015 · May 8, 2015 · Terminated
  Ethicon Fast Absorbing Plain Gut - MultiPass Needles, Sterile, Absorbable Surgical Suture, 5-0 (1.5 metric), 18" (45 cm), Conventional Cutting, Lot #JD6163, Exp: July 2019. Fast ab
• Z-0492-2015 · Oct 17, 2014 · Terminated
  Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet Ethicon LLC- Made in USA.