Vortex Surgical Inc. recalls specific disposable surgical forceps and cannulas due to potential voids in Tyvek pouch seals that could cause infection. Affected items include models VS0740.23, VS0740.25, and others with specific UDI and lot numbers.
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 Inc. is recalling certain disposable surgical forceps and cannulas because the Tyvek pouch seals may have voids that could allow contamination, leading to infection. This is a serious risk for medical procedures where sterile conditions are critical.
The Tyvek pouches used to maintain sterility may have small holes or gaps that allow bacteria to enter. This contamination could lead to infections during surgical procedures if the instruments are used without proper sterilization.
Healthcare professionals using these specific surgical instruments in medical procedures are most at risk. Patients undergoing surgery with affected products could face infection.
Check for model numbers like VS0740.23, VS0740.25, VS0744.25, and others listed in the recall. Also look for specific UDI (Unique Device Identification) numbers and lot numbers provided in the recall notice.
Identify the model number on the product, such as VS0740.23 or VS0740.25, to determine if it is affected.
Check the Unique Device Identification (UDI) number and lot number on the pouch to see if it matches the affected items listed in the recall.
The recall is due to potential voids in the Tyvek pouch seals that could lead to bioburden contamination and infection during surgical procedures.
Affected products include specific forceps and cannulas with model numbers like VS0740.23, VS0740.25, VS0744.25, and others with corresponding UDI and lot numbers listed in the recall notice.
Check the model number on the product and the UDI and lot numbers on the pouch. If they match the affected items listed in the recall, the product is affected.
We’ve drafted a message you can send Vortex to request your refund or repair — edit it as you like.
Subject: Recall Z-1247-2026 — Vortex Vortex Hello, I own a Vortex that is covered by recall Z-1247-2026 from Vortex. 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.
