Recall StatusTerminated
Date Initiated2014-06-03
Date Terminated2017-05-17
Product Quantity10,467 units
Reason for Recall
The product can be difficult to remove from the Distal Stem both out of the package and after proximal reaming.
Firm Action
DePuy Synthes sent an Urgent Information - Device Correction Notice letter dated June 24, 2014, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to:
1. Immediate Remedy: Discard the RECLAIM Taper Sleeve Protector instrument before stem implantation.
2. Changes to the literature and IFU: Documents are revised as follows:
" RECLAIM Revision Hip Systems Surgical Technique # DSUS/JRC/0614/0200 pages 11, 12, 13, 16,
30, 34, 35 (figure numbering from pages 11 to 27 were also revised): Removed information regarding
taper sleeve protector.
" RECLAIM Revision Hip Systems Surgical Technique FAQ # DSUS/JRC/0614/0202 pages 1 and 2:
Removed information regarding taper sleeve protector.
" RECLAIM Revision Hip Systems IFU #090200799 REV E Page 5: Verbiage will be revised and
implemented as soon as possible, depending on regulatory approvals.
3. Change: The company consulted with design surgeons and developed a strategy to eliminate the taper sleeve protector from the system. As a result of removing the taper sleeve protector, the company is
evaluating whether there is a need for a protective component to be used during the distribution
Customers with questions were instructed to call 574-371-4917.
For questions regarding this recall call 574-371-4577.
Distribution Pattern
Worldwide Distribution - USA including AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI & WV and Internationally to AUSTRALIA, AUSTRIA, CANADA, CHILE, CHINA, CZECH REPUBLIC, DENMARK, FRANCE, GERMANY, IBERIA, IRELAND, ISRAEL, ITALY, NEW ZEALAND, NORWAY, POLAND, SINGAPORE, SLOVENIA, SOUTH AFRICA, SPAIN, SWITZERLAND & UK.
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.