Activbody, Inc. Recalls

Overview of recall records associated with Activbody, Inc., including dates, categories and classifications where available.

2recall records

Dec 22, 2021latest record date

Dec 22, 2021earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceDec 22, 2021

Activbody Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual recall — FDA Z-0385-2022

Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing to register and list its…

Class IIFDA: OngoingActivbody, Inc.

Medical DeviceDec 22, 2021

Activbody activforce 2 package labeling: Model: Activ5-M R 201-200563 recall — FDA Z-0386-2022

Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing to register and list its…

Class IIFDA: OngoingActivbody, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Activbody, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.