Medline recalls medical procedure kits that may contain non-sterile products if the breather pouch seal is opened. Affected kits include specific models and lot numbers. Consumers should check their kits and contact Medline for details.
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 could lead to using non-sterile products if the breather pouch seal is opened. This poses a risk of infection during medical procedures if the seal is compromised.
The breather pouch seal on these kits may open unintentionally, allowing non-sterile products to be used. This could lead to infections during medical procedures if the seal is broken.
Healthcare professionals and medical facilities using the recalled Medline kits are most at risk. Patients undergoing procedures with these kits could face infection if non-sterile products are used.
Check for the product labels: ABDOMINAL HYSTERECTOMY TEGH-LF (lot 23LBP056), HYSTEROSCOPY PACK (lot 24ABG706), PERI GYN PACK (lot 23LBL679), or HYSTEROSCOPY TRAY ACS (lot 24ABB984).
Inspect the breather pouch seal for any signs of being opened or unsealed.
Reach out to Medline for specific instructions on how to handle the recalled kits.
Yes, the kits are safe to use if the breather pouch seal remains unopened and unsealed.
Discard the kit immediately and contact Medline for further instructions.
These kits are used for abdominal hysterectomy, hysteroscopy, and perigyn procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0176-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0176-2025 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.
