Synthes Material Mix (Adjustable Cervical Distractor-Right, Matrix Distractor Rack, T-PAL Spacer Remover, Implant Inserter) Synthes Material Mix: Adjustable Cervical Distractor-Right is used to distract spine segment. Matrix Distractor Rack is used to distract the interbody disc space. T-PAL Spacer Remover is used to remove T-PAL spacer. Implant Inserter is used to insert the ProDisc implant.
FDA Recall Z-0393-2014 · Posted 2013-11-26
Recalling FirmSynthes USA HQ, Inc.
Recall StatusTerminated
Product CodeLXH
Date Initiated2013-10-15
Date Terminated2015-08-31
Product Quantityapproximately 44
Reason for Recall
One material batch used for production of the affected parts of the Synthes Material Mix were mixed in with an incorrect material with a lower than specified hardness and corrosion resistance.
Firm Action
SYNTHES sent an Urgent Notice: Medical Device Recall letter dated October 15, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to call Synthes at 1-800-479-6329 to obtain a Return Authorization Number. Complete the Verification Section at the end of the letter by checking the appropriate box indicating affected product was located. Customers were also asked to indicate the number of devices found and note the Return Authorization Number. Return the Verification Form with the product to:
Credit/Returns
Synthes
1101 Synthes Avenue
Monument, CO 80132
Customers should also return the Verification Form if no affected product was found in their inventory.
Return all documents to Synthes by fax: 888-679-4875 or Scan/email: [email protected]
Customers with questions were instructed to call 610-719-5450 or contact their Synthes Sales Consultant.
For questions regarding this recall call 610-719-5000.
Root Cause
Nonconforming Material/Component
Distribution Pattern
Worldwided Distribution: USA (nationwide) including IL, MO, TX, WA and Internationally to Canada and Switzerland.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.