Device recall

Z-1925-2021: reSET Mobile App, iOS and Android, provides cognitive behavioral therapy, as…

FDA device recall · Class II · Pear Therapeutics, Inc.

Key facts

Recall number (Z-number) Z-1925-2021
Recall event 88061
Product reSET Mobile App, iOS and Android, provides cognitive behavioral therapy, as part of substance abuse treatment.
Product code PWE
Recalling firm Pear Therapeutics, Inc.
Recall class Class II
Status Terminated
Termination date Jun 14, 2023
510(k) numbers K173681
FEI number 3014109807

At a glance

  • 1–9 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

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