Reported Jun 5, 2013 · Terminated

Tibial baseplate,cemented,#1 2203-3010 Tibial baseplate,cemented,#2 2203-3020 Tibial baseplate,cemented,#3 2203-3030…

Orthopedic Alliance LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Orthopedic Alliance LLC · 26157 Jefferson Ave · Murrieta, CA · 92562-9561

Is this the product you have?

66 of 66 products

Products covered by this recall
Model / numberProduct as published
2203-3010Tibial baseplate,cemented,#1
2203-3020Tibial baseplate,cemented,#2
2203-3030Tibial baseplate,cemented,#3
2203-3040Tibial baseplate,cemented,#4
2203-3050Tibial baseplate, cemented, #5
2203-3060Tibial baseplate, cemented, #6
2303-1211Tibial insert,CR,plained,#1,9mm
2303-1212Tibial insert,CR,plained,#1,11mm
2303-1213Tibial insert,CR,plained,#1,13mm
2303-1214Tibial insert,CR,plained,#1,15mm
2303-1215Tibial insert,CR,plained,#1,18mm
2303-1221Tibial insert,CR,plained,#2,9mm
2303-1222Tibial insert,CR,plained,#2,11mm
2303-1223Tibial insert,CR,plained,#2,13mm
2303-1224Tibial insert,CR,plained,#2,15mm
2303-1225Tibial insert,CR,plained,#2,18mm
2303-1231Tibial insert,CR,plained,#3,9mm
2303-1232Tibial insert,CR,plained,#3,11mm
2303-1233Tibial insert,CR,plained,#3,13mm
2303-1234Tibial insert,CR,plained,#3,15mm
Lot codes and dates
  • Catalog No.

    66 of 66 codes

    • 2203-3010
    • 2203-3020
    • 2203-3030
    • 2203-3040
    • 2203-3050
    • 2203-3060
    • 2303-1211
    • 2303-1212
    • 2303-1213
    • 2303-1214
    • 2303-1215
    • 2303-1221
    • 2303-1222
    • 2303-1223
    • 2303-1224
    • 2303-1225
    • 2303-1231
    • 2303-1232
    • 2303-1233
    • 2303-1234
    • 2303-1235
    • 2303-1241
    • 2303-1242
    • 2303-1243
    • 2303-1244
    • 2303-1245
    • 2303-1251
    • 2303-1252
    • 2303-1253
    • 2303-1254
    • 2303-1255
    • 2303-1261
    • 2303-1262
    • 2303-1263
    • 2303-1264
    • 2303-1265
    • 2303-3011
    • 2303-3012
    • 2303-3013
    • 2303-3014
    • 2303-3015
    • 2303-3021
    • 2303-3022
    • 2303-3023
    • 2303-3024
    • 2303-3025
    • 2303-3031
    • 2303-3032
    • 2303-3033
    • 2303-3034
    • 2303-3035
    • 2303-3041
    • 2303-3042
    • 2303-3043
    • 2303-3044
    • 2303-3045
    • 2303-3051
    • 2303-3052
    • 2303-3053
    • 2303-3054
Amount recalled
459 units

This recall covers 9 products

The agency filed one notice per product. You are reading one of them; the other 8 are below.

Where it was sold

Why it was recalled

The recall of the Loaner Bin and Sterilization Trays for implants and instruments was initiated by Orthopedic Alliance because the directions for use and surgical techniques were not being provided to every physician and for every surgery.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 26, 2014 · Data as of Sep 19, 5:30 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.