--- title: "AMD Medicom Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search AMD Medicom Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/amd-medicom-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # AMD Medicom Inc. recall records **5** reported ongoing 5 records in this archive. Latest source date May 8, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status May 8, 2026 FDA device enforcement ### [Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in, Non-Sterile/55994C; 0.75x0.75in, Non-Sterile/55995C; 1.0x1...](https://isitonrecall.com/recall/fda-device-z-2458-2026-ritmed-neurological-sponges-description-ref-0-5x0-5in-non-sterile-55992c-0-5x1-0in-non-sterile-55993/) 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. Elevat... Class II Reported ongoing Distribution: US: MT, NC, VA, CA, TX, OH, TN, IL, RI [Official source for Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Steri...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2458-2026%22) May 8, 2026 FDA device enforcement ### [Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 85995C](https://isitonrecall.com/recall/fda-device-z-2459-2026-ritmed-neurological-sponges-0-75x0-75in-sterile-ref-85995c/) 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. Elevat... Class II Reported ongoing Distribution: US: MT, NC, VA, CA, TX, OH, TN, IL, RI [Official source for Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 85995C](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2459-2026%22) Dec 21, 2023 FDA device enforcement ### [HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)](https://isitonrecall.com/recall/fda-device-z-1146-2024-henry-schein-criterion-earloop-masks-level-3-blue-item-code-570-2448/) Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initial qualification of the products. Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, IA, IN, PA, NV, TX. [Official source for HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1146-2024%22) Dec 21, 2023 FDA device enforcement ### [HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-3281)](https://isitonrecall.com/recall/fda-device-z-1147-2024-henry-schein-criterion-anti-fog-earloop-masks-level-3-blue-item-code-570-3281/) Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initial qualification of the products. Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, IA, IN, PA, NV, TX. [Official source for HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-3281)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1147-2024%22) Dec 21, 2023 FDA device enforcement ### [PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG, ASTM LEVEL 3 (BLUE) (item code 127-7573)](https://isitonrecall.com/recall/fda-device-z-1148-2024-patterson-procedure-earloop-masks-anti-fog-astm-level-3-blue-item-code-127-7573/) Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initial qualification of the products. Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, IA, IN, PA, NV, TX. [Official source for PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG, ASTM LEVEL 3 (BLUE) (item code 127-7573)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1148-2024%22) ## Reasons in these listed records - 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 ... - Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initial qualification of the products. These examples come from this result page and are not a ranking of every recall reason. ## Checking AMD Medicom Inc. ### Is there a recall on amd medicom inc. right now? This archive contains 5 records, including 5 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search AMD Medicom Inc.](https://isitonrecall.com/check/?q=AMD%20Medicom%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)