American Contract Systems recalls BASIN SET MEBS42K surgical kits due to labeling error where contents don't match package label. Affected units have specific batch numbers and expiration dates.
Basin Set labeling error: components within the kit are for the Single Basin Set. Therefore, the contents of the package do not match the contents listed on the label.
American Contract Systems is recalling a surgical basin set (MEBS42K) because the items inside don't match what's listed on the label. This mismatch could lead to confusion during medical procedures if the wrong components are used.
The labeling error means the surgical kit contains components intended for a single basin set, not the multi-basin version. This mismatch could cause incorrect usage during procedures if the wrong parts are selected.
Surgical teams and hospitals that purchased the MEBS42K basin set with batch number 833221 (expiring June 2023) are likely affected. Medical professionals using the kit without verifying contents may face confusion.
Check for the model MEBS42K, batch number 833221, and expiration date June 2023 on the product label or packaging. The kit is sold as a general surgical basin set.
Check the product label for model MEBS42K, batch number 833221, and expiration date June 2023.
The recall is due to a labeling error where the contents of the kit do not match what's listed on the label.
Check the product label for model MEBS42K, batch number 833221, and expiration date June 2023. No action is needed if the product matches the label.
The recall is for labeling error, not a safety hazard. There is no risk of injury from using the product correctly.
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-0274-2023 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-0274-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
