Covidien LP (formerly Nellcor Puritan Bennett Inc.): Medical Device Recall in 2015 - (Recall #: Z-2267-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

OxiMax N-65 Handheld Pulse Oximeter. N65, N65-1, N65P, and N65P-1. For continuous or spot check monitoring of functional arterial oxygen saturation (SpO2) and pulse rate.

Product Classification:

Class II

Date Initiated: June 29, 2015

Date Posted: August 5, 2015

Recall Number: Z-2267-2015

Event ID: 71583

Reason for Recall:

Potential missing segments on the display that can result in misinterpretation of data.

Status: Terminated

Product Quantity: 211,426 units

Code Information:

All Lots of Product Code N650, N65, N65-1, N65P, N65P-1

Distribution Pattern:

Worldwide Distribution - US Nationwide including Canada.

Voluntary or Mandated:

Voluntary: Firm initiated