TSRH(R) Spinal System SCREW, REF 837-645, Size: 6.5mm x 45mm, Mat'l: TITANIUM ALLOY, Rx only, QTY: 1 EA, Medtronic Sofamor Danek USA. Product Usage: TSRH(R) Spinal System is intended to help provide immobilization of spinal segments as an adjunct to fusion of the thoracic, lumber, and/or sacral spine.
FDA Recall Z-3044-2011 · Posted 2011-08-19
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Recalling FirmMedtronic Sofamor Danek USA Inc
Recall StatusTerminated
Product CodeKWP
Date Initiated2011-07-12
Date Terminated2012-07-20
Product Quantity17 units
Reason for Recall
Screws are 5 mm longer than the size etched on the screw.
Firm Action
On 07/12/2011, the recalling firm, Medtronic notified the Sales Managers and Sales Force by conference call and email regarding the imminent notification and follow-up activities. A "VOLUNTARY RECALL" notification letter was sent to Risk Managers and Sales Representatives on 07/13/2011 with a delivery date of 07/14/2011. The letter states to immediately remove the recalled product from use and return to Medtronic. The letter includes a questionnaires form to be completed and returned as per the instructions. If appropriate, personal follow up with Sales Representatives will be made to assure that Risk Managers understand the recall communication and to facilitate return of product and the associated questionnaire documentation.
For questions, contact your Medtronic Sales Representative or the Global Quality Department at 800-876-3133, extension 3173.
Root Cause
Error in labeling
Distribution Pattern
Nationwide Distribution (USA) including the states of: OH, NY, and WI
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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