Recall
FDAHealthDecember 16, 2025

Vortex Surgical Inc. — Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
December 16, 2025

Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CT, FL, HI, IA, IL, IN, KY, MA, MI, MN, MS, NC, NE, NJ, NM, NY, OH, OR, PA, RI, SC, SD, TN, TX, WA, WI, VA; and OUS (foreign) to countries of: Australia, Chile, China, France, Germany, India, Ireland, Italy, Japan, Korea, Mexico, Netherlands, Philippines, Poland, Puerto Rico, Spain, Switzerland, Taiwan, United Kingdom, Vietnam.

What's affected?

Product
Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25
Lot code
2410044

Additional details

Pouch UDI 810123480456 Box UDI 810123480739 Lot 2410044

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 14,789 (8651 US; 6138 OUS).

View original FDA notice →

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