- Recalling firm
- ConvaTec, Inc
- Reason for recall
- Surgical dressing manufactured out of specification (greater thickness).
- Affected products (lot / model / serial)
- Lot/Batch: 5G00809; Primary Pack UDI: (01) 00768455130764/ Secondary Pack UDI: (01) 00768455130634/ Tertiary Pack UDI: (01) 10768455130631
- Units affected
- 4230 units
- Distribution pattern
- US Nationwide distribution in the states of MD, OH, IL, NC, AZ, NY, MN, TX, KS, TN, IN, DE, MI, FL, PA, CA, VA, MS, NM, GA, CO.
- Firm location
- Greensboro, NC, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2677-2026
- Recall initiated
- June 8, 2026
- FDA classification date
- July 7, 2026
- FDA report date
- July 15, 2026
- FDA event ID
- 99151
- Last updated on HTM Vibe
- July 23, 2026