ETHIBOND EXCEL CX30DRecalls & reported problems

Summary

The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 10705031024267), received between Jun 4, 2025 and Jun 4, 2025 — classified as 10 malfunctions.

The most frequently reported specific device problem is “Material Separation” (10 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 10 most recent of 10 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22145150 ↗
• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22145149 ↗
• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22145148 ↗
• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22145144 ↗
• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22145143 ↗
• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22144993 ↗
• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22144967 ↗
• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22144964 ↗
• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22144963 ↗
• MalfunctionJun 4, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A TOTAL KNEE ARTHROPLASTY (TKA) PROCEDURE ON (B)(6) 2025 AND SUTURE WAS USED. DURING THE PROCEDURE, IT WAS REPORTED TO THE REP THAT MANY OF THE NEEDLES IN THE MULTIPACK EITHER POPPED OFF WHILE REMOVING FROM THE PACK OR POPPED OFF WHILE SUTURING UNKNOWN TISSUE. ANOTHER MULTIPACK OF SUTURE WAS USED TO CONTINUE WITH THE PROCEDURE. THREE STERILE SAMPLES FROM THE PACK AND FIVE DETACHED NEEDLES WITH NO SUTURE. NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22144962 ↗

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.