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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Ethicon Inc. VICRYL RAPIDE; Suture, Absorbable, Synthetic

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Ethicon Inc. VICRYL RAPIDE; Suture, Absorbable, Synthetic Back to Search Results
Catalog Number VR494
Medical Device Problem Codes Material Separation (1562); Material Twisted/Bent (2981)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 06/30/2026
Type of Reportable Event Malfunction
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Brand Name
VICRYL RAPIDE
Common Device Name
Suture, Absorbable, Synthetic
Manufacturer (Section D)
Ethicon Inc.
1000 route 202
raritan NJ 08869
Manufacturer (Section G)
Ethicon Inc.-Brazil
rodovia presidente dutra
km 154
sao paulo 12240
BR   12240
Manufacturer Contact
orla o'mahony
1000 route 202
raritan, NJ 08869
+1(303)552-6892
MDR Report Key50060742
Report Number2210968-2026-07545
Device Sequence Number16124093
Product Code GAM
UDI-Device Identifier10705031134683
UDI-Public(01)10705031134683(17)300331(10)AW5504
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
K033746
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional
Type of Report Initial,Followup
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Catalogue NumberVR494
Device Lot NumberAW5504
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 07/06/2026
Supplement Date Received by Manufacturer08/12/2026
Initial Report FDA Received Date07/28/2026
Supplement Report FDA Received Date09/01/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured04/09/2025
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
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