Medline recalls specific OB and delivery procedure kits that could allow non-sterile products if the breather pouch seal is opened. Affected kits have unique 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 certain medical procedure convenience kits that may allow non-sterile products to be used if the breather pouch seal is opened. This could lead to infections or other health risks 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 infections or other health risks during medical procedures if the seal is compromised.
Healthcare providers and medical facilities that use these kits are most at risk. Patients using these kits during procedures could be exposed to non-sterile products.
Check for the product labels: OB PACK-LF (REF DYNJ0912449M), OB PACK (REF DYNJ17309G), or other listed kits. Look for lot numbers like 23LBP185, 24ABB399, or similar in the product description.
Inspect the breather pouch seal for any signs of being opened or unsealed.
If the pouch seal is open or unsealed, discard the kit immediately to prevent non-sterile product use.
The affected kits include OB PACK-LF (REF DYNJ0912449M), OB PACK (REF DYNJ17309G), OB PK (REF DYNJ34268D), and other listed medical procedure convenience kits with specific lot numbers.
Check the product label for the reference codes and lot numbers listed in the recall notice, such as REF DYNJ0912449M with lot number 23LBP185.
Discard the kit immediately to prevent using non-sterile products.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0177-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0177-2025 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.
