American Contract Systems recalls sterile surgical gowns made in an unregistered FDA facility. These packs (AGD1401, WPP147H, SVOH38N) may not meet safety standards. Consumers should check lot numbers and expiration dates.
The surgical gowns were manufactured in a facility that is not registered by the FDA.
American Contract Systems is recalling sterile surgical gowns used in procedures because they were made in a facility not registered with the FDA. This could mean the gowns don't meet safety standards, potentially putting patients at risk during surgery.
The gowns were manufactured in a facility not registered by the FDA. This means they may not meet safety standards for surgical use, which could lead to complications during procedures.
Surgical teams and hospitals that use these specific sterile surgical packs. Patients undergoing surgery are at risk if the recalled packs are used.
Check for ACS Tray Numbers: AGD1401 (72 kits, exp 06/31/2020), WPP147H (6 kits, exp 03/31/2020), SVOH38N (20 kits, exp 11/12/2020), and SVOH38N (4 kits, exp 10/04/2020).
Look for lot numbers like 647191, 685191, 684191, or 723191 on the surgical packs.
The gowns were manufactured in a facility not registered by the FDA, which may mean they don't meet safety standards for surgical use.
Check for ACS Tray Numbers: AGD1401 (72 kits, exp 06/31/2020), WPP147H (6 kits, exp 03/31/2020), SVOH38N (20 kits, exp 11/12/2020), and SVOH38N (4 kits, exp 10/04/2020).
The recall does not require immediate stop use; check lot numbers to determine if your gowns are affected.
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-2172-2020 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-2172-2020 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.
