Zimmer VerSys Hip System Femoral Head, 12/14 taper, 28 mm dia., neck length +0 mm, sterile, Zimmer, Warsaw, IN; REF 8018-28-02. Intended for mating femoral stems equipped with tapered necks.
FDA Recall Z-0198-2010 · Posted 2009-11-13
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Recalling FirmZimmer Inc.
Recall StatusTerminated
Product CodeLPH
Date Initiated2009-08-03
Date Terminated2009-12-15
Product Quantity104
Reason for Recall
Manufacturing material may be present on the surface of the implant.
Firm Action
An Urgent: Device Recall letter, dated 8/3/2009, was issued to consignees. The letter identified the affected product, stated the reason for the recall, the clinical implications (risks to health), and actions to be taken. Customers are to locate any unused devices and quarantine them immediately, carry out a physical count of affected product and record the data on the Return Certification Form included with the letter, and fax a copy of the completed form back to Zimmer, Inc. at 574-372-4265. Customers are to return the recalled product along with the completed Inventory Return Certification Form. A "Dear Surgeon" letter will be issued to any hospitals where the devices have been implanted.
Root Cause
Manufacturing material removal
Distribution Pattern
Worldwide Distribution -- USA, Brazil, Canada, and Switzerland.
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.
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