Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to Several shipments of Vitagel product (a surgical hemostat)...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Orthovita, Inc., dBA Stryker Orthobiologics. directly.
Affected Products
Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.
Quantity: 274
Why Was This Recalled?
Several shipments of Vitagel product (a surgical hemostat) required to be stored at 2 -8 degrees Celsius (C) were not delivered to customers within the validated delivery time.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Orthovita, Inc., dBA Stryker Orthobiologics.
Orthovita, Inc., dBA Stryker Orthobiologics. has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report