—#75748

Product

Zimmer Minimally Invasive Solutions Technology Offset Rasp Handle, Right, 30 degrees, Zimmer, Warsaw, IN; REF 00-7806-035-02. The offset rasp handle is a surgical instrument used with various sizes of femoral rasps to prepare the femoral canal for a hip implant.

FDA product code: LXH — Orthopedic Manual Surgical Instrument
Device class: Class 1
Medical specialty: Orthopedic
Affected lot / code info: Lot Numbers: 60244767, 60254985, 60270484, 60283990, 60291761, 60295682,60298345, 60327534, 60332316, 60337990, 60347614, 60363922, 60395585, 60406637, 60416986, 60453034, 60468964, 60482887, 60517611, 60688076 and 60810866.

Why it was recalled

The c-clip located near the connection end may fracture or fall off during use in surgical procedures.

Root cause (FDA determination)

Labeling design

Action the firm took

U.S. consignees were notified by "Urgent: Device Recall" letter issued via e-mail on December 19, 2008. The letter described the problem and instructed customers to immediately quarantine and return the recalled product along with the completed Inventory Return Certification form to the Zimmer, Inc. Distribution Center. Consignees were also instructed to fax a copy of the completed Inventory Return Certification Form at 1-574-371-8603. International consignees were also notified, but Zimmer, Inc. will gather the instruments from those customers. Direct questions about the recall to Zimmer, Inc. at 1-800-613-6131.

Recalling firm

Firm: Zimmer Inc.
Address: 345 E Main St, Warsaw, Indiana 46580-2746

Distribution

Distribution pattern: Worldwide Distribution --- including USA, Belgium, Czech Republic, Finland, Germany, Greece, Italy, Poland, Romania, Spain and United Kingdom.

Timeline

Recall initiated: 2008-12-19
Posted by FDA: 2009-02-27
Terminated: 2009-12-22
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #75748. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.