Respire Medical: Medical Device Recall in 2018 - (Recall #: Z-1947-2018)

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:

Respire Pink Series EF+ Oral Sleep Apnea Device.

Product Classification:

Class II

Date Initiated: September 1, 2017

Date Posted: June 6, 2018

Recall Number: Z-1947-2018

Event ID: 80030

Reason for Recall:

Potential for device breakage during use

Status: Terminated

Product Quantity: 1 unit

Code Information:

Serial Number: 50837

Distribution Pattern:

US nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated