FDA Medical Device Recalls (openFDA)
Ethicon, Inc.: Coated VICRYL Polyglactin 910 Suture VIO 36IN(90CM) USP0(M3.5) S/A CT, Product Number J358H
- Recall number
- Z-0319-2025
- Recalling firm
- Ethicon, Inc.
- Product
- Coated VICRYL Polyglactin 910 Suture VIO 36IN(90CM) USP0(M3.5) S/A CT, Product Number J358H
- Status
- Open, Classified
- Initiated
- 2024-09-25
- Posted
- 2024-11-07
- Terminated
- not on file
- Reason
- 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.
- Root cause
- Under Investigation by firm
- Action
- An URGENT: FIELD SAFETY NOTICE was sent to customers beginning on 9/25/24. ACTION REQUIRED 1. Examine your inventory immediately to determine if you have product subject to this recall on hand and quarantine such product(s). If you have product subject to this recall, please maintain a copy of this notice with the quarantined product and keep a copy for your records. 2. Communicate the issue to relevant operating room or materials management personnel, or anyone else in your facility who needs to be informed. If any product subject to this recall has been forwarded to another facility, contact that facility to arrange return. Please consider including a copy of this recall letter when communicating. 3. Complete the Business Reply Form (BRF) (Attachment 3) confirming receipt of this notice and fax or email to [Enter Affiliate Information] within three (3) business days. Please return the BRF even if you do not have product subject to this recall. 4. Customers are required to return unused VICRYL" (polyglactin 910) Suture subject to this recall that are in inventory immediately. To receive credit or replacement product as appropriate, customers must return product subject to this recall no later than December 31, 2024 to [Enter Affiliate Information]. Any non-affected product and any product returned after the date specified will not be eligible for credit or replacement product. 5. Keep this notice visibly posted for awareness until all product subject to this recall has been returned to [Enter Affiliate Information]. If you require any assistance with
- Quantity
- 31,032 units
- Distribution
- International distribution to the country of China.
- Lot, serial or model codes
- UDI-DI: 10705031237308 (each); 30705031237302 (box); Lot Number: QP2AJM
- 510(k) numbers
- ["K183183"]
- PMA numbers
- not on file
- Product code
- GAM
- Firm FEI
- 3017102971
- Firm city
- Raritan
- Firm state
- NJ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28