Sofsilk GS-47-MRecalls & reported problems
Covidien LP · Wax Coated Braided Silk · Class 2 · Implant
All models of Sofsilk (120)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10884521085039), received between Mar 12, 2019 and Dec 10, 2019 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (3 reports).
13 other recalls cover devices cleared under the same FDA submission (K981128); 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
- Break3
- Detachment of Device or Device Component1
Patient problems
- No Consequences Or Impact To Patient3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 10, 2019Break; Break
ACCORDING TO THE REPORTER, DURING A TOTAL PAROTIDECTOMY PROCEDURE, THE NEEDLE OF THE EIGHT SUTURES WERE BROKEN. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9443587 ↗MalfunctionOct 22, 2019Break; Break
ACCORDING TO THE REPORTER, DURING A TOTAL PAROTIDECTOMY PROCEDURE, THE NEEDLE OF THE SUTURE WAS BROKEN. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9222019 ↗MalfunctionMar 12, 2019Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
ACCORDING TO THE REPORTER, DURING A LAMINECTOMY PROCEDURE, THE NEEDLE TIP BROKE OFF AND WENT INTO THE PATIENT'S CAVITY WHILE THE OTHER HALF OF THE NEEDLE FELL TO THE OR FLOOR. THE NEEDLE TIP IN THE PATIENT WAS IMMEDIATELY SEEN AND RETRIEVED BY THE SURGEON AND THE CIRCULATOR NURSE PICKED UP THE OTHER HALF OF THE NEEDLE ON THE FLOOR. ANOTHER SUTURE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8412549 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K981128. One submission often covers many models, so check the product and lot details in each record.
- Z-1697-2024 · Jan 25, 2024 · Open, ClassifiedSofsilk Braided Silk sutures, Product Number S-2782K. Nonabsorbable, sterile, non-mutagenic surgical suture composed of natural silk fibers, for use in soft tissue approximation an
- Z-0845-2024 · Dec 21, 2023 · Open, ClassifiedSofsilk Braided Silk sutures: CS-211 SOFSILK* 4-0 BLK 45CM CVF21 X36 GS-831 SOFSILK* 4-0 BLK 75CM V20 X36 S-176 SOFSILK* 0 BLK 12X45CM PCT X24 S-182 SOFSILK* 5-0 BLK 12X45CM PCT X
- Z-1176-2023 · Dec 2, 2022 · Open, ClassifiedSofsilk Coated Braided Silk Suture Product Description CS-211 SOFSILK* 4-0 BLK 45CM CVF21 X36 CS211 CS-490 SOFSILK* 2-0 BLK 75CM GS11 X36 CS490 CS-562 SOFSILK* 2-0 BLK 75C
- Z-2810-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 0 18" BLACK GS-21 DT non-absorbable braided nylon sutures CS10M Sofsilk is intended for use in general soft tissue approximation and/or ligation, including use i
- Z-2812-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 5/0 BLACK 5 X 18" CV-22 D*TACH non-absorbable silk sutures GS43M Sofsilk is intended for use in general soft tissue approximation and/or ligation, including use
- Z-2819-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 0 BLACK 6X 18" PRE-CUT WAX/RACE non-absorbable braided nylon sutures S196 Sofsilk is intended for use in general soft tissue approximation and/or ligation, inclu
- Z-2811-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 3/0 18" BLACK CV-25 DT non-absorbable silk sutures GS33M Sofsilk is intended for use in general soft tissue approximation and/or ligation, including use in the c
- Z-2815-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 2/0 BLACK 5x18" V-20 D-TACH non-absorbable silk sutures GS62M Sofsilk is intended for use in general soft tissue approximation and/or ligation, including use in
- Z-2814-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 4/0 18" BLACK CV-22 DT non-absorbable silk sutures GS46M Sofsilk is intended for use in general soft tissue approximation and/or ligation, including use in the c
- Z-2818-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 3/0 BK 12X18" PRE-CUT WAX-RACE non-absorbable braided nylon sutures S194 Sofsilk is intended for use in general soft tissue approximation and/or ligation, includ
- Z-2813-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 4/0 18" BLACK CV-22 DT non-absorbable silk sutures GS44M Sofsilk is intended for use in general soft tissue approximation and/or ligation, including use in the
- Z-2816-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 3/0 18" BLACK V-20 DT non-absorbable braided nylon sutures GS63M Sofsilk is intended for use in general soft tissue approximation and/or ligation, including use
- Z-2817-2011 · Jun 3, 2011 · TerminatedSyneture Sofsilk 2/0 30" BLACK V-20 DT non-absorbable braided nylon sutures GS66M Sofsilk is intended for use in general soft tissue approximation and/or ligation, including use
Other SUTURE, NONABSORBABLE, SILK devices
- Sofsilk S-2782KCovidien LP · SUTURE, NONABSORBABLE, SILK3 recalls0 reports
- PERMA-HAND SA86GEthicon, LLC · SUTURE, NONABSORBABLE, SILK120 reports
- Sofsilk S-1768KCovidien LP · SUTURE, NONABSORBABLE, SILK2 recalls5 reports
- Sofsilk S-316Covidien LP · SUTURE, NONABSORBABLE, SILK2 recalls2 reports
- Sofsilk S-304Covidien LP · SUTURE, NONABSORBABLE, SILK2 recalls2 reports
- Sofsilk S-187Covidien LP · SUTURE, NONABSORBABLE, SILK2 recalls1 report
- Sofsilk S-605Covidien LP · SUTURE, NONABSORBABLE, SILK2 recalls1 report
- Sofsilk S-176Covidien LP · SUTURE, NONABSORBABLE, SILK2 recalls0 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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