Recall StatusOpen, Classified
Date Initiated2026-03-31
Product Quantity260,962
Reason for Recall
Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water flow from distal tip under unsupported third-party connector use conditions, which may lead to water aspiration, which may progress to aspiration pneumonia, acute respiratory distress syndrome, or respiratory failure.
Firm Action
On 3/31/2026, correction notices were emailed to Medical Directors, Risk Managers, Medical Device Safety Officers, or Healthcare Professionals informing them to take the following actions:
1) Discontinue use of unsupported third-party Scope Port Connectors.
2) Provide this notice to all personnel within your organization who use, service, purchase, stock, or otherwise manage.
3) If you further distributed any affected devices, promptly forward this notice to those
accounts and request that they take the same actions.
4) Continue following the instructions for use, including verifying connector compatibility, ensuring that all connectors are fully seated, confirming that all joints and interfaces are secure, and verifying correct placement and alignment of the tubing within the pump head.
5) Utilize the compatibility table in the notice until updated Notes on Use is received.
6) Complete and return the response form via email to
[email protected].
Firm contacts: Correction:
[email protected], 480-564-1899. Routine Customer Service and Complaints:
[email protected], 1-800-778-3723
Root Cause
Component change control
Distribution Pattern
US Nationwide distribution including in the states of IL, NY, CA, WA, UT, KY, PA, TX, AL, OH, FL, IN, NJ, NH, MI, CT, AR, MN, WI, AZ, CO, WV, MT, HI, TN, GA, VA, OK, RI, MO, NM, ID, SC, WY, KS, NC, MS, OR, MD, MA, DE, NE, AK, IA, DC, ME, LA, SD, ND, VT, PR, NV.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.