Device recall

Z-2115-2017: NexGen Offset Stem Extension, sizes 14mm and 17mm For use in total arthroplasty.

FDA device recall · Class II · Zimmer Biomet, Inc.

Key facts

Recall number (Z-number) Z-2115-2017
Recall event 77140
Product NexGen Offset Stem Extension, sizes 14mm and 17mm For use in total arthroplasty.
Product code JWH
Recalling firm Zimmer Biomet, Inc.
Recall class Class II
Status Terminated
Termination date Jul 3, 2018
510(k) numbers K933785
FEI number 1000220733

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 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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