The Fuhrman Pleural/Pneumopericardial Drainage Set The Fuhrman Pleural/Pneumopericardial Drainage Set consists of pigtail catheter, access needle, dilator, and wire guide. The set also includes a multipurpose tubing adapter, and three-way stopcock.
FDA Recall Z-0478-2016 · Posted 2016-01-04
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Recalling FirmStryker Sustainability Solutions
Recall StatusTerminated
Product CodeKDQ
Date Initiated2015-11-17
Date Terminated2016-09-28
Product Quantity34 devices
Reason for Recall
Stryker Sustainability Solutions is recalling the Fuhrman Pleural & Pneumopericardial Drainage Set due to receiving complaints that it broke off in the pleural cavity while inserting the device into the patient.
Firm Action
The firm, Stryker Sustainability Solutions, sent a "URGENT MEDICAL DEVICE RECALL" letter dated 11/17/2015 to its customers. The letter identified the product, problem, and actions to be taken by the customers. Customers were instructed to discontinue the use of the product, and complete the Recall Effectiveness Check Form even if no product has been found in inventory. Customers should return the completed Recall Effectiveness Check Form to their local Stryker Sustainability Sales Representative, email to [email protected], or mail to: Stryker Sustainability Solutions, 1810 West Drake Drive,Tempe, AZ 85283.
If the firm indicates that affected devices remain in inventory, a prepaid shipping label will be issued for the return of the product. Customers will receive credit for all affected devices returned.
Adverse reactions or quality problems experienced with the use of this product
may be reported to:
- Stryker Sustainability Solutions Complaint Hotline: +1(888) 888-3433x5555
- http://www.stryker.com/productexperience/
- The FDAs MedWatch Adverse Event Reporting program either online, by
regular mail, or by fax.
If you have any questions, contact Senior Regulatory Affairs Specialist at (888) 888-3433x5506 or email: [email protected].
Root Cause
Device Design
Distribution Pattern
US Distribution in the states of: AK, CA, WI, IN, FL, OR, NY, and NC.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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