Medline recalls sterile surgical kits with weak pouch seals that could breach sterility. Affected kits have specific model numbers and lot codes. 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, it could breach the sterility of the contents, potentially leading to infections during surgery.
The Pure Pouch component has weak seals that may fail under normal use conditions. If the seal breaches, the sterile contents could become contaminated, increasing the risk of infection during surgical procedures.
Surgical staff and hospitals using Medline Retrograde PK-22025203-LF kits with pack number DYNJ47873L are most at risk. These kits are used in sterile surgical procedures where contamination could cause serious infections.
Check for the model number Medline Retrograde PK-22025203-LF and pack number DYNJ47873L. The kit contains a Pure Pouch with a Sterile Curved Kelly Hemostat. Lot numbers 23KBW512 and expiration date 8/31/2027 are also identifiers.
Discard the affected surgical kit to prevent potential contamination and infection risks.
The recalled kits are Medline Retrograde PK-22025203-LF with pack number DYNJ47873L.
If the seal fails, the sterility of the surgical contents could be breached, leading to potential infections during procedures.
Check for the model number Medline Retrograde PK-22025203-LF and pack number DYNJ47873L. The kit contains a Pure Pouch with a Sterile Curved Kelly Hemostat.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2225-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2225-2024 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.
