Reported Jun 5, 2013 · Terminated
Femoral component, CR, cemented, #1, left 2103-1310 Femoral component, CR, cemented, #2, left 2103-1320 Femoral…
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?
24 of 24 products
| Model / number | Product as published |
|---|---|
2103-1310 | Femoral component, CR, cemented, #1, left |
2103-1320 | Femoral component, CR, cemented, #2, left |
2103-1330 | Femoral component, CR, cemented, #3, left |
2103-1340 | Femoral component, CR, cemented, #4, left |
2103-1350 | Femoral component, CR, cemented, #5, left |
2103-1360 | Femoral component, CR, cemented, #6, left |
2103-1410 | Femoral component, CR, cemented, #1, right |
2103-1420 | Femoral component, CR, cemented, #2, right |
2103-1430 | Femoral component, CR, cemented, #3, right |
2103-1440 | Femoral component, CR, cemented, #4, right |
2103-1450 | Femoral component, CR, cemented, #5, right |
2103-1460 | Femoral component, CR, cemented, #6, right |
2103-3110 | Femoral component, PS, #1, left |
2103-3120 | Femoral component, PS, #2, left |
2103-3130 | Femoral component, PS, #3, left |
2103-3140 | Femoral component, PS, #4, left |
2103-3150 | Femoral component, PS, #5, left |
2103-3160 | Femoral component, PS, #6, left |
2103-3210 | Femoral component,PS, #1, right |
2103-3220 | Femoral component,PS, #2, right |
- Lot codes and dates
- Catalog No.
2103-13102103-13202103-13302103-13402103-13502103-13602103-14102103-14202103-14302103-14402103-14502103-14602103-31102103-31202103-31302103-31402103-31502103-31602103-32102103-32202103-32302103-32402103-32502103-3260
- Catalog No.
- Amount recalled
- 136 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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