Z-1098-2025 Class II Ongoing
FDA device recall Z-1098-2025 was initiated by Ethicon, LLC on Dec 20, 2024 and is designated Class II. Reason for recall: Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could introduce pathogens to… The recall status is ongoing. Affected quantity: 48.
Recall details
- Product Type
- Devices
- Report Date
- Feb 12, 2025
- Initiation Date
- Dec 20, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 48
Product description
ETHIBOND EXCEL Polyester Suture, REF: 6664H, X425H, X872H, EH7491H. Not sold in US
Reason for recall
Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could introduce pathogens to the patient and cause infection.
Distribution pattern
Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, LA MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI and the countries of AT, AU, BE, CA, CH, CN, CZ, DE, DK, FI, FR, GB, HU, IE, JP, LU, NL, NO, PL, SE, SG, ZA.
Code information
REF/GTIN/Lot(expiration): W8003T/10705031231658/103GT2(8/31/2029)
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1098-2025
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026