Recall
FDAHealthDecember 16, 2025

Vortex Surgical Inc. — Vortex Surgical 25GA Backflush, VS0270.25; 25GA Backflush Retractable, VS0275.27

⚠️ 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 Backflush, VS0270.25; 25GA Backflush Retractable, VS0275.27
Lot code
2411017

Additional details

25GA Backflush Pouch UDI 810123480470 Box UDI 810123480753 Lot 2411017; 27GA Backflush Retractable Pouch UDI 810123480517 Box UDI 810123480791 Lot 2411016

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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