Every recall we track for AMD Medicom Inc. — 7 in all — plus the complaints and injury reports the public filed about them.
AMD Medicom recalls Ritmed Neurological Sponges (0.75x0.75in) due to potential endotoxin levels that could cause neurovascular issues during surgery. Affected units have specific serial numbers and lot codes.
AMD Medicom recalls Ritmed Neurological Sponges (0.5x0.5in to 1.0x3.0in) due to potential endotoxin levels that could cause neurovascular issues during surgery. Affected lots distributed after May 2022.
Henry Schein recalls blue Level 3 anti-fog earloop masks (item 570-3281) produced on unvalidated equipment. These masks may not meet safety standards due to production issues.
Henry Schein recalls Level 3 blue earloop masks (item 570-2448) produced on unvalidated equipment. These masks may not meet safety standards due to production issues.
AMD Medicom Inc. recalls anti-fog earloop masks (item code 127-757: blue, ASTM Level 3) made on unvalidated equipment. These masks may not meet safety standards.
Medicom recalls Level 3 masks (Item Code 2042) that may have been packed with lower protection level masks. Using these could lead to inadequate protection during use.
Medicom recalls Level :2 masks (Item 2040) that may be in Level 3 boxes. Using these masks risks lower protection than intended. Affected masks were sold with Lot 1917.
