Recall
FDAHealthDecember 16, 2025

Vortex Surgical Inc. — 25GA Subretinal Injection Cannula VS0220.25

⚠️ 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
25GA Subretinal Injection Cannula VS0220.25
Lot code
2410043

Additional details

Pouch UDI 810123480418 Box UDI 810123480692 Lot 2410043

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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