Medline recalls TUBAL LIGATION PACKs with specific lot numbers due to potential non-sterile product if the breather pouch seal is opened. Affected kits may not be safe for medical procedures.
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 TUBAL LIGATION PACKs because the breather pouch seal could be opened, risking non-sterile product. This could lead to infections or complications during medical procedures if the pouch seal is compromised.
The breather pouch seal on these kits may open, allowing non-sterile product to be used. This could happen if the vendor seal is broken during handling or storage, potentially leading to infections or complications during medical procedures.
Healthcare providers using Medline TUBAL LIGATION PACKs with lot number 24ABG688 are affected. Those performing medical procedures with these kits are at risk of using non-sterile products.
Check for lot number 24ABG688 on the Medline TUBAL LIGATION PACK. The product is a medical procedure convenience kit with reference number DYNJ66230B.
Inspect the breather pouch seal for any signs of being opened or unsealed.
The product may not be safe if the breather pouch seal is opened, as it could result in using non-sterile product.
The official recall notice does not specify a remedy, so check the pouch seal for any signs of being opened.
Look for lot number 24ABG688 on the Medline TUBAL LIGATION PACK with reference number DYNJ66230B.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0170-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0170-2025 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.
