Medical DeviceOct 1, 2014
Vapotherm Precision Flow,Disposable Patient Circuit PFNODPC-High recall — FDA Z-2702-2014
Disposable Patient Circuit that allows water to leak into the center gas lumen
Class IIFDA: TerminatedVapotherm, Inc.
Recall history in this database
Classification mix: Class II: 8.
Medical DeviceOct 1, 2014
Vapotherm Precision Flow,Disposable Patient Circuit PF-E-DPC-High recall — FDA Z-2700-2014
Disposable Patient Circuit that allows water to leak into the center gas lumen
Class IIFDA: TerminatedVapotherm, Inc.
Medical DeviceOct 1, 2014
Vapotherm Precision Flow, Disposable Patient Circuit PF-DPC-High recall — FDA Z-2699-2014
Disposable Patient Circuit that allows water to leak into the center gas lumen
Class IIFDA: TerminatedVapotherm, Inc.
Medical DeviceOct 1, 2014
Vapotherm Precision Flow,Disposable Patient Circuit PFHDPC-Low recall — FDA Z-2705-2014
Disposable Patient Circuit that allows water to leak into the center gas lumen
Class IIFDA: TerminatedVapotherm, Inc.
Medical DeviceOct 1, 2014
Vapotherm Precision Flow,Disposable Patient Circuit PF-NODPC-Low recall — FDA Z-2706-2014
Water may leak into the center gas lumen of the Patient Circuit
Class IIFDA: TerminatedVapotherm, Inc.
Medical DeviceOct 1, 2014
Vapotherm Precision Flow,Disposable Patient Circuit PF-DPC-Low recall — FDA Z-2703-2014
Disposable Patient Circuit that allows water to leak into the center gas lumen
Class IIFDA: TerminatedVapotherm, Inc.
Medical DeviceOct 1, 2014
Vapotherm Precision Flow,Disposable Patient Circuit PF-E-DPC-Low recall — FDA Z-2704-2014
Disposable Patient Circuit that allows water to leak into the center gas lumen
Class IIFDA: TerminatedVapotherm, Inc.
Medical DeviceOct 1, 2014
Vapotherm Precision Flow,Disposable Patient Circuit PFH-DPC-High recall — FDA Z-2701-2014
Disposable Patient Circuit that allows water to leak into the center gas lumen
Class IIFDA: TerminatedVapotherm, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Vapotherm, 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.