Biosyn CM-914Recalls & reported problems
Covidien LP · Monofilament Absorbable Suture,GS-24,1x Violet Strand · Class 2 · Implant
All models of Biosyn (94)
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 10884521032156), received between Sep 17, 2020 and Feb 25, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (3 reports).
28 other recalls cover devices cleared under the same FDA submission (K000037); 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
Most reported problems
Device problems
- Detachment of Device or Device Component3
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 25, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT DURING A PROCEDURE, THE SUTURE DETACHED FROM THE NEEDLE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24444549 ↗MalfunctionFeb 25, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT DURING A CESARIAN-SECTION PROCEDURE, IN THE CLOSING STEP, THE SUTURE DETACHED FROM THE NEEDLE WHILE SUTURING AFTER THE PATIENT INCISION. THE NEEDLE DID NOT FALL INTO THE PATIENT CAVITY. AN ADDITIONAL NEW SUTURE WAS USED WITHOUT ISSUE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24444392 ↗MalfunctionSep 17, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
ACCORDING TO THE REPORTER, WHEN THE DEVICE WAS BEING APPLIED TO THE UTERUS FOR THE FIRST STAGE OF CLOSURE DURING A CAESAREAN SECTION, THE NEEDLE DETACHED FROM THE THREAD AND FELL INTO THE UTERUS. THE UTERUS WAS RE-OPENED AND THE NEEDLE WAS RETRIEVED AND THE CONTINUED TO CLOSE. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10548455 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K000037. One submission often covers many models, so check the product and lot details in each record.
- Z-1298-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 0 30" VIOLET GU-46, Item Code UL877 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not i
- Z-1286-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 2-0 VIOLET 30" V-20, Item Code GL123 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not
- Z-1291-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 6/0 12"" VL SS-24 D/A, Item Code L1742K - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but n
- Z-1275-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 0 30" UNDYED HOS-11, Item Code CL537 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not
- Z-1274-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 3/0 VIOLET 30" CV-24 (75CM), Item Code CL461 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery,
- Z-1277-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 3/0 30 VIOLET GS-11, Item Code CL815 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not
- Z-1276-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 2/0 30 VIOLET GS-21, Item Code CL811 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not
- Z-1284-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 1 36 VIOLET GS-21, Item Code CL925 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in
- Z-1288-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 2/0 UNDYED 30" V-30 (75CM), Item Code GL228 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, b
- Z-1278-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 1 30 VIOLET GS-22, Item Code CL885 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in
- Z-1289-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 2-0 UNDYED 30" V-20, Item Code GL323 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not
- Z-1295-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture UD 4/0 18 P-13, Item Code SL5690 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in c
- Z-1293-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 6/0 18" UNDYED P-10, Item Code SL1625G - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but no
- Z-1279-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture 13-0 VIOLET 30" GS-23, Item Code CL892 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but no
- Z-1294-2020 · Dec 18, 2019 · TerminatedPolysorb Braided Absorbable Suture UD 3/0 30 P-14, Item Code SL5679 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in c
…and 13 more.
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- V-Loc 180 VLOCL0604Covidien LP · SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID1 recall328 reports
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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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