Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vasc. Open CVOR SJH Recalled by American Contract Systems, Inc. Due to During an internal investigation, ACS identified that the...
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 American Contract Systems, Inc. directly.
Affected Products
Vasc. Open CVOR SJH, REF SJVO56B
Quantity: 84 cases
Why Was This Recalled?
During an internal investigation, ACS identified that the components, I.V. Cath (part number 4252535-02) and Adhesive Dermabond (part number DHVM12) were inadvertently subjected to the ACS sterilization process and exposed to EO and higher temperatures than approved by the component manufacturer. As a result, the components may (1) have a loss/lack of functionality, (2) loss of drug efficacy, if applicable, and (3) have higher than specified EO residuals.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About American Contract Systems, Inc.
American Contract Systems, Inc. has 90 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report