AMD Medicom Inc. recalls
5 federal recalls on file, showing the 2 from the last 12 months. We monitor every CPSC, FDA, USDA, and NHTSA notice for AMD Medicom Inc. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-06-24FDA-DeviceClass IIRitmed Neurological Sponges recalled for endotoxin risk
AMD Medicom Inc. is recalling Ritmed Neurological Sponges (0.75x0.75in, Sterile, REF: 85995C) used during brain surgery because some units may not meet safety standards for endotoxin—a bacterial byproduct that can cause harmful reactions in the cerebrospinal fluid. Elevated endotoxin levels could lead to fever, inflammation, low blood pressure, nausea, or neurological complications.
- 2026-06-24FDA-DeviceClass IIRitmed Neurological Sponges recalled for endotoxin risk
Ritmed Neurological Sponges used during brain surgery may contain elevated endotoxin levels. Endotoxins are bacterial contaminants that can trigger inflammation, fever, or temporary blood pressure drops when sponges contact cerebrospinal fluid during surgery.
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