American Contract Systems recalls Neuro Vascular medical kits due to potential humidity problems that could impact sterilization. Affected units have specific lot and expiration details.
ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm product sterilization assurance requirements were met.
American Contract Systems is recalling a medical convenience kit because humidity readings in one area may not meet sterilization standards. This could mean the kit isn't properly sterilized, which is a serious risk for medical use.
The kit's humidity readings in one controlled area are out of specification. This could mean the product wasn't properly sterilized, which is critical for medical use.
Healthcare professionals using the Neuro Vascular kit for medical procedures may be affected. Those with the specific lot number and expiration date are most at risk.
Check for the lot number 2405102 and expiration date 05/10/2025 on the kit. The product name is Neuro Vascular, ANKV91A.
Look for the lot number 2405102 and expiration date 05/10/2025 on the kit.
The recall is because humidity readings in one controlled area were out of specification, which may mean the kit wasn't properly sterilized.
Check the lot number and expiration date. If it matches 2405102 and 05/10/2025, contact American Contract Systems for more information.
The recall record does not mention any remedy or fix for this issue.
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-3236-2024 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-3236-2024 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.
