Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203 Recalled by Stryker Sustainability Solutions Due to Product defect; tip of two (2) Angiographic Catheters...
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 Stryker Sustainability Solutions directly.
Affected Products
AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203
Quantity: 167
Why Was This Recalled?
Product defect; tip of two (2) Angiographic Catheters model # 10732203 broke off, prior to being used on the patient.
Where Was This Sold?
This product was distributed to 11 states: CA, CT, MD, MA, NY, PA, TX, UT, VT, VA, WA
About Stryker Sustainability Solutions
Stryker Sustainability Solutions has 38 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report