WECK IPN921609Recalls & reported problems
Teleflex Incorporated · Class 1
All models of WECK (97)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 22
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 22 adverse event reports that list this exact device (DI 14026704727480), received between Dec 2, 2025 and Jul 20, 2026 — classified as 22 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (11 reports).
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 Component11
- Device Dislodged or Dislocated9
- Material Deformation2
Patient problems
- No Clinical Signs, Symptoms or Conditions22
Recent adverse event reports
The 22 most recent of 22 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 20, 2026Device Dislodged or Dislocated
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25881897 ↗MalfunctionJul 20, 2026Device Dislodged or Dislocated
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25877992 ↗MalfunctionJul 20, 2026Device Dislodged or Dislocated
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25876951 ↗MalfunctionJun 19, 2026Device Dislodged or Dislocated
IT WAS REPORTED "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25562970 ↗MalfunctionJun 19, 2026Device Dislodged or Dislocated
IT WAS REPORTED "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25562963 ↗MalfunctionJun 19, 2026Device Dislodged or Dislocated
IT WAS REPORTED "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25562485 ↗MalfunctionJun 19, 2026Device Dislodged or Dislocated
IT WAS REPORTED "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25562357 ↗MalfunctionJun 19, 2026Device Dislodged or Dislocated
IT WAS REPORTED "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25562267 ↗MalfunctionJun 19, 2026Device Dislodged or Dislocated
IT WAS REPORTED "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25562219 ↗MalfunctionApr 6, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24795414 ↗MalfunctionApr 6, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24795153 ↗MalfunctionMar 20, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24651758 ↗MalfunctionMar 20, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24651407 ↗MalfunctionMar 18, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24628314 ↗MalfunctionMar 18, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24627842 ↗MalfunctionMar 13, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI. " NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24592724 ↗MalfunctionFeb 10, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI". NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24307298 ↗MalfunctionFeb 10, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI". NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24306378 ↗MalfunctionFeb 10, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI". NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24306226 ↗MalfunctionJan 21, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI". NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24138755 ↗MalfunctionDec 2, 2025Material Deformation; Material Deformation
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23694986 ↗MalfunctionDec 2, 2025Material Deformation; Material Deformation
IT WAS REPORTED THAT "A POPPED RIVET WAS IDENTIFIED DURING REPAIR AT MSI." NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23694919 ↗
Other Applier, surgical, clip devices
- LIGACLIP MCS20Ethicon Endo-Surgery, LLC · Applier, surgical, clip1 death337 reports
- Endo Clip III 176630BCovidien LP · Applier, surgical, clip312 reports
- LIGACLIP MCM20Ethicon Endo-Surgery, LLC · Applier, surgical, clip308 reports
- LIGACLIP MCM30Ethicon Endo-Surgery, LLC · Applier, surgical, clip1 death236 reports
- WECK IPN915189Teleflex Incorporated · Applier, surgical, clip221 reports
- LIGACLIP MSM20Ethicon Endo-Surgery, LLC · Applier, surgical, clip152 reports
- LIGACLIP LX107Ethicon Endo-Surgery, LLC · Applier, surgical, clip105 reports
- WECK IPN028280Teleflex Incorporated · Applier, surgical, clip93 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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