American Contract Systems recalls DR DIULUS injection packs with model numbers CCDU12C, CCDU12D, and CCDU12D-01 due to possible failure in sterilization assurance, which may cause treatment delays or complications.
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 DR DIULUS injection packs with specific model numbers because they may not have been properly sterilized. This could lead to delays or complications in medical treatments if the packs are used.
The injection packs may not have been properly sterilized during manufacturing, which could lead to contamination. This might cause treatment delays or complications if the packs are used without proper sterilization.
Patients using these injection packs for medical treatments are likely affected. Healthcare providers who use the packs for injections may also be at risk.
Check for model numbers CCDU12C, CCDU12D, or CCDU12D-01 on the injection packs. The packs were sold with specific tray lots and dates as listed in the recall notice.
Identify the model number on the injection pack to confirm if it is one of CCDU12C, CCDU12D, or CCDU12D-01.
American Contract Systems cannot confirm that the injection packs were properly sterilized, which may lead to treatment delays or complications.
Model numbers CCDU12C, CCDU12D, and CCDU12D-01 are affected.
The recall notice does not specify a remedy, so you should check the product model and contact American Contract Systems for further instructions.
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-1332-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1332-2025 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.
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.
