Brand Name: U2 Total Knee System Product Name: PSA Box Trial, L, #1-6 and PSA Box Trial, R, #1-6 Model/Catalog Number: 9323-5511 thru 9323-5516 and 9323-5521 thru 9323-5526 Software Version: N/A Product Description: Knee femur prosthesis trial, reusable Component: No, N/A
FDA Recall Z-2883-2026 · Posted 2026-08-05
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Recalling FirmUnited Orthopedic Corp.
Recall StatusOpen, Classified
Product CodeJWH
Date Initiated2026-05-20
Product Quantity2
Reason for Recall
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Firm Action
On 03/11/2026, the firm emailed an "URGENT: MEDICAL DEVICE RECALL" Letter to customers informing them that due the fact that the PSA Box Trial cannot be properly assembled with the Hinge Trial in the affected devices because of incomplete processing of the screw components, which may result in interference during assembly with the corresponding device.
On 05/20/2026, the firm emailed an updated "URGENT: MEDCIAL DEVICE RECALL" Letter
Customers are instructed:
1. Examine your inventory immediately to locate the affected product whose quantities and lot numbers are listed above. Please note the product may have already been returned.
2. Cease all use of these devices immediately and quarantine all affected devices in your territory for immediate return.
3. Customer Service will be contacting you regarding replacements. If you still have the product, you are requested to immediately return the affected product using the prepaid airbills on RMA XXXX .
a. Write the RMA number on the outside of the box clearly and legibly.
b. Ship recalled product via Fed Ex standard overnight to:
UOC USA INC.
Attention: RMA# XXXX
16601 Hale Ave. Irvine, CA 92606
(Attached Shipping Label)
4. Additionally, if your firm has further distributed the recall product, please provide that customer with a copy of this recall notification and assist them with the return of the product.
5. Complete and return the following page according to the instructions.
For Question - contact UOC Sr. Director of Sales Operations at 949.328.3366.
Root Cause
Process design
Distribution Pattern
US Nationwide distribution in the states of Texas and Michigan.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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