Nellcor Puritan Bennett Inc. ( recalls

Nellcor Puritan Bennett Inc. ( has 11 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 17 Dec 2014. The most frequent reason is device malfunction.

Total recalls11since 2012
Last 12 months0reported
Class I327% of total
Ongoing0latest 17 Dec 2014

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 3 27%Class II 8 73%Class III 0 0%

Why nellcor puritan bennett inc. ( is recalled

Product types

By year

All nellcor puritan bennett inc. ( recalls, newest first

11 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS ICovidien Puritan Bennett 980 Ventilator recalledNellcor Puritan Bennett Inc. (OtherNationwide
DeviceCLASS ICovidien Puritan Bennett 980 Ventilator recalledNellcor Puritan Bennett Inc. (Lead & Heavy Metals17 states
DeviceCLASS IIVital Sync RMS 0 when loaded with v2.4 recalledNellcor Puritan Bennett Inc. (Packaging Defects8 states
DeviceCLASS IIVital Sync" VPMP & IM recalled by Nellcor Puritan Bennett Inc. (Nellcor Puritan Bennett Inc. (Packaging Defects8 states
DeviceCLASS IIPuritan Bennett 840 Ventilator recalledNellcor Puritan Bennett Inc. (Device MalfunctionNationwide
DeviceCLASS IIModel Number(s): PB840 Ventilator recalledNellcor Puritan Bennett Inc. (Device MalfunctionNationwide
DeviceCLASS IIproduct is a component of the Newport Medical Instruments recalledNellcor Puritan Bennett Inc. (Device Malfunction16 states
DeviceCLASS IIPuritan Bennett 840 Series Ventilator PB840 Operators recalledNellcor Puritan Bennett Inc. (Device MalfunctionNationwide
DeviceCLASS IIPuritan Bennett 700 Series Ventilators (PB740 recalledNellcor Puritan Bennett Inc. (Device MalfunctionNationwide
DeviceCLASS IIDgphp RFA High-Power Single Use Grounding Pads recalledNellcor Puritan Bennett Inc. (Potency & AssayNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.