Medline recalls certain medical procedure convenience kits that may allow non-sterile product use if the breather 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 medical procedure convenience kits that could lead to using non-sterile products if the breather pouch seal is opened. This poses a risk of infection or contamination during medical procedures.
The breather pouch seal on these kits can be opened or unsealed, allowing non-sterile products to be used. This could lead to contamination during medical procedures, increasing infection risks.
Medical professionals and facilities using the recalled Medline procedure kits are most at risk. Patients receiving procedures with these kits could face infection risks.
Check for the product labels: PAIN PROCEDURE PACK (REF DYNJ80370A) or DR HEFZY BLOCK TRAY (REF DYNJRA1854A). Look for lot numbers 23LBM330 or 23LBJ089.
Ensure the breather pouch seal is intact before use to prevent non-sterile product exposure.
The breather pouch seal can be opened or unsealed, allowing non-sterile products to be used during medical procedures.
Lot numbers 23LBM330 for PAIN PROCEDURE PACK and 23LBJ089 for DR HEFZY BLOCK TRAY.
Look for the product labels: PAIN PROCEDURE PACK (REF DYNJ80370A) or DR HEFZY BLOCK TRAY (REF DYNJRA1854A) with lot numbers 23LBM330 or 23LBJ089.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0153-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0153-2025 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.
