Medline recalls neuro and shunt procedure kits with breather pouches that may allow non-sterile product use if the pouch seal is opened. Affected kits have specific lot numbers and references.
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Medline is recalling neuro and shunt procedure kits that could allow non-sterile products to be used if the breather pouch seal is opened. This poses a risk of infection or contamination during medical procedures.
The breather pouches in these kits have a seal that may open or become unsealed, allowing non-sterile products to be used. This could lead to infections or contamination during medical procedures if the pouch is not properly sealed.
Healthcare professionals using Medline neuro and shunt procedure kits with specific lot numbers are most at risk. Patients receiving procedures using these kits could also be affected.
Check for the product labels: NEURO PACK (REF DYNJ37909A) or SHUNT PACK (REF DYNJ40040C). Look for lot numbers 24ABG035 or 23KBB863 on the packaging.
Ensure the breather pouch seal is intact before use to prevent non-sterile product exposure.
Medline neuro packs (REF DYNJ37909A, lot 24ABG035) and shunt packs (REF DYNJ40040C, lot 23KBB863).
Check for the product labels and lot numbers: NEURO PACK (REF DYNJ37909A) with lot 24ABG035 or SHUNT PACK (REF DYNJ40040C) with lot 23KBB863.
Ensure the breather pouch seal is intact before use to prevent non-sterile product exposure.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0173-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0173-2025 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.
