CLASS II Device recall · Reported 5 Jun 2013 · FDA Enforcement Report
Uknee Patella,small 2401-1010 Uknee Patella,medium recalled
Orthopedic Alliance is recalling Uknee Patella,small 2401-1010 Uknee Patella,medium 2401-1020 Uknee Patella,large, distributed nationwide in the US. The recall was initiated on 20 Feb 2013 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1380-2013
- FDA event ID
- 64588
- Recalling firm
- Orthopedic Alliance, Murrieta, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 20 Feb 2013
- FDA classified
- 24 May 2013
- Reported
- 5 Jun 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Device type
- Hip & Knee Implants
Timeline
| 20 Feb 2013 | Recall initiated by company | |
| 24 May 2013 | Classified by FDA | +93 days |
| 5 Jun 2013 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
UKNEE Patella,small 2401-1010 UKNEE Patella,medium 2401-1020 UKNEE Patella,large 2401-1030 UKNEE Patella,X-large 2401-1040 UKNEE Onset Patella, 3 pegs, x-small 2403-1010 UKNEE Onset Patella, 3 pegs, small 2403-1020 UKNEE Onset Patella, 3 pegs, medium 2403-1030 UKNEE Onset Patella, 3 pegs, large 2403-1040 UKNEE Onset Patella, 3 pegs,X-large 2403-1050 Variety of hip and knee implants and instruments, multiple uses.
Where it was distributed
Nationwide Distribution including the states of CA, MD, TX, NV, and WI.
Questions about this recall
Why was it 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.
Which lots are affected?
Catalog No. 2401-1010 2401-1020 2401-1030 2401-1040 2403-1010 2403-1020 2403-1030 2403-1040 2403-1050
Where was it sold?
Nationwide Distribution including the states of CA, MD, TX, NV, and WI.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
8 other products · FDA event 64588| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Tibial baseplate,cemented,#1 2203-3010 Tibial recalled | Orthopedic Alliance | Sterility | Nationwide | |
| CLASS II | U2 Acetabular cup, Ti beads porous coated recalled | Orthopedic Alliance | Sterility | Nationwide | |
| CLASS II | Zweimueller Type Stem Scs-Standard Sz 01 Zweimueller Type recalled | Orthopedic Alliance | Sterility | Nationwide | |
| CLASS II | Ball Head, 28 Short Ceramic Ball Head recalled by Orthopedic Alliance | Orthopedic Alliance | Sterility | Nationwide | |
| CLASS II | Co-Cr cancellous bone screw Co-Cr cancellous bone screw recalled | Orthopedic Alliance | Sterility | Nationwide | |
| CLASS II | Bipolar Cap, ID26mm, OD42mm Bipolar Cap, ID28mm recalled | Orthopedic Alliance | Sterility | Nationwide | |
| CLASS II | Femoral head, standard, ¿, + Femoral head,medium recalled | Orthopedic Alliance | Sterility | Nationwide | |
| CLASS II | Femoral component, CR, cemented, #1 recalled by Orthopedic Alliance | Orthopedic Alliance | Sterility | Nationwide |
More recalls from Orthopedic Alliance
All 10| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Femoral component, CR, cemented, #1 recalled by Orthopedic Alliance | Orthopedic Alliance | Sterility | Nationwide |
| Device | CLASS II | Femoral head, standard, ¿, + Femoral head,medium recalled | Orthopedic Alliance | Sterility | Nationwide |
| Device | CLASS II | Bipolar Cap, ID26mm, OD42mm Bipolar Cap, ID28mm recalled | Orthopedic Alliance | Sterility | Nationwide |
| Device | CLASS II | Co-Cr cancellous bone screw Co-Cr cancellous bone screw recalled | Orthopedic Alliance | Sterility | Nationwide |
| Device | CLASS II | Ball Head, 28 Short Ceramic Ball Head recalled by Orthopedic Alliance | Orthopedic Alliance | Sterility | Nationwide |
Other Hip & Knee Implants recalls
All 3,097| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Medline convenience kits labeled as: Femoral Pack, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Arvis Surgical Navigation System Gen recalled by Kico Knee Innovation | Kico Knee Innovation | Nitrosamine Impurity | 19 states |
| Device | CLASS II | Veritas Standard Reverse Total Shoulder Veritas Standard recalled | restor3d | Device Malfunction | Nationwide |
| Device | CLASS II | Endo-Model, Replacement Set, Tibial Plateau, right/left, L, Uhmwpe recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Lead & Heavy Metals | IN |
| Device | CLASS II | U2 Total Knee System Femoral offset bushing recalled | United Orthopedic | Device Malfunction | Nationwide |