Vortex Surgical recalls 25GA Backflush pouches with specific model numbers and lots due to potential seal voids causing infection risk. Affected items may need replacement to prevent contamination.
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.
Vortex Surgical is recalling specific 25GA Backflush pouches that may have seal voids, risking infection. This is serious because medical devices must stay sterile to prevent infections during procedures.
The pouches may have voids in their seal, which could allow bacteria to enter. This breaks the sterile barrier needed for safe medical procedures, potentially causing infections.
Surgical staff and hospitals using the recalled pouches for procedures. Those handling the specific model numbers and lots are most at risk.
Check for model numbers VS0270.25 or VS0275.27 on the pouch. Look for lot numbers 2411017 or 2411016 on the box. The pouches are used in surgical procedures.
Identify the model number on the pouch (VS0270.25 or VS0275.27) to confirm if it's affected.
Check the box for lot numbers 2411017 or 2411016 to determine if the pouch is part of the recall.
The pouches may have voids in their seal, which could allow bacteria to enter and cause infection during medical procedures.
Check the model number on the pouch (VS0270.25 or VS0275.27) and the lot number on the box (2411017 or 2411016).
The recall does not require immediate stop use; affected pouches should be checked and replaced if they match the model and lot numbers.
We’ve drafted a message you can send Vortex Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1255-2026 — Vortex Surgical Vortex Surgical Hello, I own a Vortex Surgical that is covered by recall Z-1255-2026 from Vortex Surgical. 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.
