Device recall

Z-0112-2022: Flower Drill Bit Kit 2.4 mm-intended to be used with solid 2.4mm screws and can…

FDA device recall · Class II · Flower Orthopedics Corporation

Key facts

Recall number (Z-number) Z-0112-2022
Recall event 88669
Product Flower Drill Bit Kit 2.4 mm-intended to be used with solid 2.4mm screws and can be used with any plate as part of the Flower Small and Medium Implant Set and uses the small locking mechanism. Catalog Number: DBK 024
Product code HTW
Recalling firm Flower Orthopedics Corporation
Recall class Class II
Status Terminated
Termination date Feb 16, 2023
FEI number 3009996260

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

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