Exact FDA event identifier

Event 62415

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket: March 21, 2011
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Stryker Spine

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

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.

Z-2176-2012

Recall number: Z-2176-2012
Initiated: March 21, 2011
Classification: Class II
Status: Terminated
Recalling firm: Stryker Spine
Quantity: 109 Lots

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Catalog Number: 48361223, 48361224, 48361225, 48361226, 48361227, 48361228 Lot Code: 084505, 084506, 084507, 084508, 084509, 084510

Distribution pattern

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