Recall company profile

WalkMed Infusion, LLC Recalls

Overview of recall records associated with WalkMed Infusion, LLC, including dates, categories and classifications where available.

18recall records
Jul 27, 2016latest record date
Nov 18, 2015earliest record date

Recall history in this database

Classification mix: Class II: 18.

Medical DeviceJul 27, 2016

WalkMed Infusion The pump recall — FDA Z-2220-2016

WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton Infusion Pump (model 300000) and Triton FP Infusion Pump (model 400000) Due to Unapproved Changes to the Software and…

Class IIFDA: TerminatedWalkMed Infusion, LLC
Medical DeviceJul 27, 2016

WalkMed Infusion The pump recall — FDA Z-2219-2016

WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton Infusion Pump (model 300000) and Triton FP Infusion Pump (model 400000) Due to Unapproved Changes to the Software and…

Class IIFDA: TerminatedWalkMed Infusion, LLC

Understanding this recall history

This page summarizes recall records in which the official source identifies WalkMed Infusion, LLC 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.