Device recall

Z-2399-2026: Hintermann Series Talar Implant, Left, Size 2 REF 302112

FDA device recall · Class II · DT MedTech, LLC

Key facts

Recall number (Z-number) Z-2399-2026
Recall event 98987
Product Hintermann Series Talar Implant, Left, Size 2 REF 302112
Product code NTG
Recalling firm DT MedTech, LLC
Recall class Class II
Status Open, Classified
PMA numbers P160036
FEI number 3012104767

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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

Browse all FDA device recalls (products)