Device recall

Z-0413-2019: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN…

FDA device recall · Class II · GE Healthcare, LLC

Key facts

Recall number (Z-number) Z-0413-2019
Recall event 81182
Product Touchscreen display kit. Sold under the following product names: TOUCHSCREEN DISPLAY KIT 11.X ENGLISH FOR USA, TOUCHSCREEN DISPLAY KIT 11.X ENGLISH, TOUCHSCREEN DISPLAY KIT 11.X GERMAN, TOUCHSCREEN DISPLAY KIT 11.X DUTCH, TOUCHSCREEN DISPLAY KIT 11.X FRENCH, TOUCHSCREEN DISPLAY KIT 11.X DANISH…
Product code BSZ
Recalling firm GE Healthcare, LLC
Recall class Class II
Status Terminated
Termination date Apr 12, 2021
510(k) numbers K110213, K170872
FEI number 2126677

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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