Device recall

Z-1123-2019: Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset…

FDA device recall · Class II · Encore Medical, Lp

Key facts

Recall number (Z-number) Z-1123-2019
Recall event 82379
Product Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF: 495-00-065, 495-00-075, 495-00-085, 495-01-065, 495-01-075, 495-01-085
Product code KWZ
Recalling firm Encore Medical, Lp
Recall class Class II
Status Terminated
Termination date Sep 16, 2020
510(k) numbers K163497
FEI number 1000116912

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

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