Recalled eye packs and cataract packs may have been exposed to unvalidated sterilization cycles, risking infection. Consumers should check serial numbers and contact the company for details.
Product was exposed to multiple sterilization cycles without validation for multiple exposures.
American Contract Systems recalls certain eye packs and cataract packs due to potential unvalidated sterilization cycles. This could lead to infection risks if the products are used without proper sterilization.
The products may have been exposed to multiple sterilization cycles without proper validation. This could mean the products are not sterile and might cause infections if used.
People who own or use the recalled eye packs or cataract packs are affected. Those with medical procedures involving these products are at higher risk.
Check the tray number, sterilization lot, lot number, and bag serial number on the product. The recalled items include specific combinations like BLSE37K, MECA21P, CMEY17AD, and CXEY80X.
Look for the tray number, sterilization lot, lot number, and bag serial number on the product packaging.
Check the tray number, sterilization lot, lot number, and bag serial number on the product. Contact American Contract Systems for further instructions.
The products may not be sterile due to unvalidated sterilization cycles, which could lead to infection risks.
Compare your product's tray number, sterilization lot, lot number, and bag serial number with the listed combinations: BLSE37K, MECA21P, CMEY17AD, CXEY80X.
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-1705-2022 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1705-2022 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.
