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Terminated

Stryker Reliance AL Implant Blocker (Various sizes) The SLIDE Implant Blocker is a reusable instrument, sterilized prior to use. It allows the surgeon to distract the disc space in the lumbar region of the spine using an anterior or anterolateral approach while also allowing them to insert the implant into final position.

FDA Recall Z-2176-2012 · Posted 2012-08-09

Recalling FirmStryker Spine
Recall StatusTerminated
Product CodeMDM
Date Initiated2011-03-21
Date Terminated2013-03-21
Product Quantity109 Lots

Reason for Recall

Stryker Spine has received six reports regarding the breakage of one or more prongs at the extremity of the instrument.

Firm Action

Stryker sent an Urgent Product Recall letters/return response forms dated April 5, 2012, via FedEX to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to examine their inventory and hospital location to identify the product. Reconcile any SLIDE Implant Blockers with catalog and lot numbers referenced above. Retrieve and return the affected product using the enclosed pre-paid mailing label to Stryker Spine 59 Route 17 South, Allendale, New Jersey, 07401. For questions customers were instructed to call 201-760-8298.

Root Cause

Component design/selection

Distribution Pattern

Nationwide Distribution including NC, AR, TN, MA, IL, GA, NY, LA, MN, MO, OH, KS, NM, TX, KS,and IN.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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