Sofsilk S-304Recalls & 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
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521086470), received between Mar 30, 2020 and Mar 19, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
2 FDA recall records name this device's identifier, 2 still open.
11 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.
Reports received per month
Recalls naming this device
- Dec 21, 2023Open, Classified
Specific lots of sutures were sterilized with gamma doses that exceeded the range approved. The extra gamma levels may decrease the strength of the sutures over time, which could result in harms such as wound dehiscence and hemorrhage/blood loss/ bleeding at a critical level.
Z-0845-2024 · Root cause: Process control · Recall details · FDA record ↗
- Dec 2, 2022Open, Classified
Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
Z-1176-2023 · Root cause: Packaging process control · Recall details · FDA record ↗
Most reported problems
Device problems
- Break2
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
- 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.
MalfunctionMar 19, 2024Break; Break
ACCORDING TO THE REPORTER, DURING A PROCEDURE, THE SUTURE THREAD WAS BROKEN.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 18937052 ↗MalfunctionMar 30, 2020Break; Break
ACCORDING TO THE REPORTER, DURING AN OPEN PROCEDURE, WHEN THE SPECIALIST USED THE FIRST AND SECOND SUTURE IN TYING, BOTH BROKE WITHOUT FINISHING THE KNOT. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9899086 ↗
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-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-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-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-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-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-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
- 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-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
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-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
- Sofsilk S-317Covidien 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 · each recall links to the FDA recall notice
- 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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