Device recall

Z-0771-06: Zimmer M/L Taper Rasp Handle, Right, 45 degrees, non-sterile; Part number…

FDA device recall · Class II · Zimmer Inc.

Key facts

Recall number (Z-number) Z-0771-06
Recall event 34634
Product Zimmer M/L Taper Rasp Handle, Right, 45 degrees, non-sterile; Part number 83-7712-035-02. Recall Z-0671-06 extended to include this product.
Product code LXH
Recalling firm Zimmer Inc.
Recall class Class II
Status Terminated
Termination date Dec 5, 2007
FEI number 1000220733

At a glance

  • None 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

Browse all FDA device recalls (products)