Signature Patient-Specific Surgical Guides; patient specific instruments used as a guide during surgical procedure for total and partial knee arthroplasty. Part of the Signature Personalized Patient Care System.
FDA Recall Z-0162-2016 · Posted 2015-10-23
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Recalling FirmMaterialise N.V.
Recall StatusTerminated
Product CodeOSF
Date Initiated2015-09-23
Date Terminated2016-02-12
Product Quantity4
Reason for Recall
Potential inaccuracies in the alignment of the guides. Surgery was inaccurately planned because the patient image data was incorrectly processed.
Firm Action
On September 16, 2015 Materialise NV identified four cases where not all available image sets were used to design the case. On September 18, 2015, prior to the surgery dates Materialise informed (phone call) the Signature
Services Manager of Zimmer Biomet that inaccuracies in the alignment of the knee might be observed with the use of the guides due to this issue. Biomet was asked to segregate the packages for these four cases and to return them to the Materialise US office. On September 23, 2015 this was
followed up by e-mail notification letter with response forms.
Biomet was requested to contact Materialise customer service to return these four cases and arrange a replacement set of patient specific surgical guides Monday through Friday, 8:00 AM to 4:30 PM, Eastern Time. E-mail : ortho-quality@materialise. be
Customer Service
Materialise USA LLC
44650 Helm Court
Plymouth, Michigan 48170
734-259-7033
Root Cause
Use error
Distribution Pattern
Distributed in MI, ID, TX, and in France.
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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