- Recalling firm
- Integra LifeSciences Corp. (NeuroSciences)
- Reason for recall
- Increased rate of out-of-specification endotoxin results.
- Affected products (lot / model / serial)
- Product ID: WSM1015. UDI-DI: 00386190001455. Lot Numbers: 7579681, 7582225, 7583893, 7582227, 7591942, 7591944, 7583935, 7594266, 7593018, 7594288, 7594284, 7593013.
- Units affected
- 452 units
- Distribution pattern
- US Nationwide distribution in the states of AL, AZ, CA, DC, FL, GA, IA, IL, KS, KY, LA, MD, ME, MN, MO, MT, NC, ND, NE, NJ, NY, OH, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV.
- Firm location
- Princeton, NJ, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1818-2026
- Recall initiated
- March 19, 2026
- FDA classification date
- April 15, 2026
- FDA report date
- April 22, 2026
- FDA event ID
- 98607
- Last updated on HTM Vibe
- July 24, 2026