HALYARD recalls Laparotomy Pack model 88231 due to elevated anti-block/slip additive residues in sterile packaging. This could compromise surgical safety. Affected units include specific lot numbers and expiration dates.
Elevated residues of anti-block/slip additive used in manufacturing found within sterile packaging.
HALYARD is recalling Laparotomy Pack model 88231 because it contains elevated residues of anti-block/slip additives in the sterile packaging. This could risk surgical safety if the packaging is compromised during use.
The sterile packaging may contain elevated residues of anti-block/slip additives from manufacturing. If these residues contaminate the surgical site during use, they could compromise the sterile field and increase infection risk.
Surgical teams and hospitals using HALYARD Laparotomy Pack model 88231 are likely affected. Patients undergoing surgery are at risk if the packaging is compromised.
Check for model number 88231 on the packaging. Affected units have lot number AC2335502D and expire by December 28, 2021.
Look for model number 88231, lot number AC2335502D, and expiration date December 28, 2021.
The recall indicates elevated residues in the packaging, which could compromise surgical safety. Affected units should be checked and handled with caution.
Check the model number and lot number on the packaging. If it matches 882335502D and expires by December 28, 2021, contact HALYARD for guidance.
Look for model number 88231, lot number AC2335502D, and expiration date December 28, 2021 on the packaging.
We’ve drafted a message you can send HALYARD to request your refund or repair — edit it as you like.
Subject: Recall Z-0983-2025 — HALYARD HALYARD Hello, I own a HALYARD that is covered by recall Z-0983-2025 from HALYARD. 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.