Recall StatusTerminated
Date Initiated2018-11-09
Date Terminated2022-05-03
Product Quantity483
Reason for Recall
4-way stopcocks and stopcock manifold assembled in certain perfusion tubing systems, indicated for use in surgical procedures requiring extracorporeal support for periods of up to six hours, may leak or be occluded.
Firm Action
On 11/09/2018 Medical Device Correction Notices were mailed to customers via UPS First Overnight. Customers were advised:
1) Inspect your stock and identify Perfusion Tubing System(s) belonging to the impacted lots in inventory, as noted in Attachment 1.
2) The recalling firm will be shipping one case of sterile stopcocks (part number: SCO4S) and manifolds (part number: 020581600) to your facility as an immediate replacement for those remaining that may be defective in your impacted Perfusion Tubing System stock.
3) As each affected pack is opened for use, please replace the original stopcocks in the pack with the spare provided by the firm. The original stopcocks should be destroyed/ discarded.
4) Contact your firm Representative if additional replacement stopcocks are required.
In addition, customers were asked to complete and return the attached Customer Response Form. Also, to assure within their organization that the correction notice is communicated to all personnel who need to be aware of it.
For questions about this Medical Device Correction, please contact (800) 986-4702 or e-mail
[email protected]
Root Cause
Process control
Distribution Pattern
Worldwide Distribution - Domestic (US) Consignees: AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, VA, WA, WI, WV, MS;
Foreign (OUS) Consignees: Canada
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.