Medline recalls Neuro IR surgical kits with weak seals that could breach sterility. Affected kits have specific pack numbers and expiration dates. Stop using immediately to prevent infection risks.
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
Medline is recalling sterile surgical convenience kits that contain a Pure Pouch with weak seals. If the seal fails, the kit's sterility could be compromised, risking infection during surgery.
The Pure Pouch component has weak seals that may fail, causing sterility breaches. This could lead to infections if the kit is used during surgery without proper sterility.
Surgical staff and hospitals using Medline Neuro IR Packs with pack numbers DYNJ56073C and specific lot numbers. Those handling the kits during procedures are most at risk.
Check for pack number DYNJ56073C on the kit. Look for lot numbers 23IDA509 (expiring May 31, 2026) or 23DDC159 (expiring November 30, 2025).
Discard the kit if you have the affected pack number and lot numbers listed.
The affected kit is Medline Neuro IR Pack with pack number DYNJ56073C.
Lot numbers 23IDA509 (expiring May 31, 2026) and 23DDC159 (expiring November 30, 2025).
Check for pack number DYNJ56073C and lot numbers 23IDA509 or 23DDC159 on the kit label.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2226-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2226-2024 from Medline. 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.
