FDA recall record

Ethicon Coated VICRYL Polyglactin 910 Suture VIO 36IN(90CM) USP0(M3.5) S/A CT, Product recall — FDA Z-0319-2025

Complaints were received regarding needle pull-off and suture degradation. Analysis on returned product from this lot confirmed that some sutures were…

Class IIclassification
Z-0319-2025official record ID
Nov 13, 2024report date

Recall record at a glance

Official recordZ-0319-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmEthicon, Inc.
Report dateNov 13, 2024
Recall initiation dateSep 25, 2024
Quantity31,032 units
LocationRaritan, NJ, United States

Official product description

Coated VICRYL Polyglactin 910 Suture VIO 36IN(90CM) USP0(M3.5) S/A CT, Product Number J358H

Why the product was recalled

Complaints were received regarding needle pull-off and suture degradation. Analysis on returned product from this lot confirmed that some sutures were visually degraded in the package.

Distribution information

International distribution to the country of China.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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