American Contract Systems recalls various C-section packs that were exposed to multiple sterilization cycles without validation, potentially leading to contamination risks. Affected items include specific tray numbers and lot codes.
Product was exposed to multiple sterilization cycles without validation for multiple exposures.
American Contract Systems is recalling several C-section packs that were sterilized multiple times without proper validation. This could lead to contamination risks during medical procedures, making it important for healthcare providers to stop using these packs immediately.
The packs were exposed to multiple sterilization cycles without validation, meaning the sterilization process wasn't properly checked for each use. This could result in the packs being contaminated with harmful bacteria or other pathogens, posing a risk of infection during surgery.
Healthcare providers using the recalled C-section packs are most at risk. These packs are typically used in surgical settings for cesarean deliveries.
Check the tray number, sterilization lot, lot number, and bag serial number on the pack. Affected items include specific combinations like LSRHPCSECTB with lot 2106301 and serial 64124711.
Immediately stop using any C-section packs with the specific tray numbers and serial codes listed in the recall notice.
The packs were exposed to multiple sterilization cycles without validation, which could lead to contamination risks during medical procedures.
Check the tray number, sterilization lot, lot number, and bag serial number on the pack. Affected items include specific combinations like LSRHPCSECTB with lot 2106301 and serial 64124711.
Immediately stop using the pack 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-1703-2022 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1703-2022 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.
