American Contract Systems recalls CV BASIC PUMP PACK Model WECV23D due to possible sterilization issues affecting treatment safety. Affected units sold with specific lot numbers.
ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
American Contract Systems is recalling CV BASIC PUMP PACKs with model number WECV23D because they may not have been properly sterilized. This could cause delays or problems with medical treatments if the pump isn't working correctly.
The pump may not be properly sterilized, which could lead to treatment delays or the pump not functioning as intended. This is a medical device that requires consistent operation for patient care.
Patients using this medical pump for treatment are most at risk. The recall affects specific model numbers and production lots sold between 2021 and 2022.
Check for model number WECV23D on the pump. Affected units have specific lot numbers: 939241, 71-050895, 71-051582, 71-052213. These were sold starting in 2021.
Look for model number WECV23D on the pump's label.
Reach out to American Contract Systems for guidance on next steps if you have the affected model.
The recall states possible loss or lack of functionality may lead to treatment delays or issues, but it does not indicate immediate danger to health.
Check for model number WECV23D and lot numbers 939241, 71-050895, 71-051582, or 71-052213.
Contact American Contract Systems directly for specific instructions on next steps.
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-1353-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1353-2025 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.