O-Two Medical Technologies, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2885-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000

Product Classification:

Class II

Date Initiated: May 14, 2018

Date Posted: August 29, 2018

Recall Number: Z-2885-2018

Event ID: 80414

Reason for Recall:

Higher levels of nitrous oxide delivered than specification

Status: Terminated

Product Quantity: 3 units

Code Information:

Serial Number: EQ1332-17, EQ3001-18, EQ3003-18

Distribution Pattern:

AK, CA, FL

Voluntary or Mandated:

Voluntary: Firm initiated