Z-2459-2026 Class II Ongoing
FDA device recall Z-2459-2026 was initiated by AMD Medicom Inc. on May 8, 2026 and is designated Class II. Reason for recall: Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification… The recall status is ongoing. Affected quantity: 10.
Recall Details
- Product Type
- Devices
- Report Date
- June 24, 2026
- Initiation Date
- May 8, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10
Product Description
Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 85995C
Reason for Recall
Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.
Distribution Pattern
US: MT, NC, VA, CA, TX, OH, TN, IL, RI
Code Information
UDI-DI: 10686864044465, Lot: 17936