Data Foundry

Medical device recalls 2013

S-LIFT Extension Shims Extension shims are manufactured from grade 5… — Class II medical device recall Z-0274-2014

Terminated recall by SpineFrontier, Inc., reported 2013-11-20, distributed nationwide. Fit variation among all lots of S-LIFT extension shims with corresponding retractor blades. The firm's investi

Recall numberZ-0274-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSpineFrontier, Inc., Beverly, MA, United States
Recall initiated2013-08-28
Classified2013-11-14
Reported by FDA2013-11-20
Terminated2018-09-13
DistributedNationwide (US)
Quantity67
Lot numbers11-50109, 11-50110, 11-50110-1, 43089, 43089R, 43092R, 46415, 46415-1, 46416, 46416-1, 50109-1, CT12H013

Product

S-LIFT Extension Shims Extension shims are manufactured from grade 5 titanium and are curved, rectangular slabs which have four protrusions used for ratcheting. They come in straight and pointed varieties, either with or without a tab containing an additional bend. Extension shims are designed to slide down retractor blades, and are optional retractor components utilized during lumbar interbody fusion procedures. They are intended to manipulate tissue and prevent tissue from interfering inside the surgical field.

Reason for recall

Fit variation among all lots of S-LIFT extension shims with corresponding retractor blades. The firm's investigation revealed that extension shims may not fit down all retractor blades.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0274-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.