FDA Medical Device Recalls (openFDA)
Ethicon, Inc.: PROLENE SUTURE 36"(90CM) 4-0 BLUE, D9067
- Recall number
- Z-2459-2018
- Recalling firm
- Ethicon, Inc.
- Product
- PROLENE SUTURE 36"(90CM) 4-0 BLUE, D9067
- Status
- Terminated
- Initiated
- 2018-05-07
- Posted
- not on file
- Terminated
- 2020-06-08
- Reason
- The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare professional handling the subject product or a patient infection due to a breach of sterility within the packaging if it goes unnoticed by the healthcare professional.
- Root cause
- Package design/selection
- Action
- On May 24, 2018, the firm distributed Urgent: Medical Device Recall letters to affected U.S. customers. Customers were instructed to do the following: 1. Examine your inventory immediately to determine if you have product subject to this recall (removal) on hand and quarantine such product(s). 2. Remove the product subject to this recall (removal) and communicate the issue to relevant operating room or materials management personnel, or anyone else in your facility who needs to be informed. 3. If any product subject to this recall (removal) has been forwarded to another facility, contact that facility to arrange return. 4. Complete the Business Reply Form (BRF) confirming receipt of this notice and fax or email it to Stericycle at 1-888-473-8015 or Ethicon3681@stericycle.com within three (3) business days. Please return the BRF even if you do not have product subject to this recall (removal). 5. Keep this notice visibly posted for awareness until all product subject to this recall (removal) has been returned to Stericycle. While processing your returns, please maintain a copy of this notice with the product subject to this recall (removal) and keep a copy for your records. 6. Customers are required to return all unused D-Special PROLENE Polypropylene Suture & D-Special PRONOVA Poly (Hexafluoropropylene - VDF) Suture products that are in their inventory immediately. Only D-Special PROLENE Polypropylene Suture & D-Special PRONOVA Poly (Hexafluoropropylene - VDF) Suture product subject to this recall (removal) returned by September 21, 2018 will be eligible for credit reimbursement. Any product subject to this recall (removal) returned after September 21, 2018 will not be eligible for credit reimbursement. 7. To return product subject to this recall (removal), photocopy the completed BRF, place it in the box with the product, and affix the pre-paid authorized shipping label included with the recall notification letter. Ethicon will pay for
- Quantity
- 1020
- Distribution
- Accounts in AZ, CA, CO, FL, GA, IL, IN, KS, MA, MN, MO, NC, NE, NJ, NY, OH, OR, SC, SD, TN, TX, VA, WA, WI, WV.
- Lot, serial or model codes
- KKJ659 LAH044 LEH699 MCH331 MDH290 MCQ536
- 510(k) numbers
- ["K133356"]
- PMA numbers
- not on file
- Product code
- GAW
- Firm FEI
- 2210968
- Firm city
- Somerville
- 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