American Contract Systems recalls specific medical procedure kits due to potential endotoxin level variations in Ritmed Neurological Sponges, which could affect surgical safety.
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
American Contract Systems is recalling certain medical procedure kits and trays because the Ritmed Neurological Sponges in them may have unexpected endotoxin levels. This could pose a risk during medical procedures if the sponges cause an adverse reaction in patients.
The Ritmed Neurological Sponges (Models 55992C-55998C) may have unexpected endotoxin levels. Endotoxins are bacterial components that can cause adverse reactions in patients during medical procedures, potentially leading to complications if the sponges are used in surgery.
Healthcare professionals using the recalled medical procedure kits and trays are most at risk, particularly those involved in spinal or cervical surgeries.
Check for kits labeled 'ANTERIOR CERVICAL PACK - 205988' (Model MHAC65AH) or 'SPINE PACK - 206013' (Model MHSP99AF). Look for specific lot numbers: 42-8606211, 42-8687611, 42-8847511, 42-8423411, 42-8470411, 42-8527611, 42-8601311, or 42-8731511, 42-8795311.
Look for the model numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
Reach out to American Contract Systems for guidance on next steps if you have the recalled items.
The recall includes medical procedure kits labeled 'ANTERIOR CERVICAL PACK - 205988' (Model MHAC65AH) and 'SPINE PACK - 206013' (Model MHSP99AF) with specific lot numbers.
The Ritmed Neurological Sponges in these kits may have unexpected endotoxin levels, which could cause adverse reactions during medical procedures.
No, the recall is for potential endotoxin variability, which is a low-risk issue. Continue using the kits but verify if they are in the recalled lot numbers.
We’ve drafted a message you can send American Contract Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2990-2026 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-2990-2026 from American Contract Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
