FDA Enforcement Class II Terminated

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER AND 7 FT. OXYGEN TUBING, REF CPRM1126F

Recall: Z-2154-2018 · Reported June 20, 2018

Enforcement

Recall Number
Z-2154-2018
Event ID
80201
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Sun Med, LLC
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
June 20, 2018
Initiation Date
May 24, 2018
Classification Date
June 9, 2018
Termination Date
May 12, 2020
Address
2710 Northridge Dr NW Ste A, N/A, Grand Rapids, MI, 49544-9112, United States

Description

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER AND 7 FT. OXYGEN TUBING, REF CPRM1126F

Reason

There is a potential for the patient port retaining ring to not fully seat allowing the patient port to detach during use. This may impact air delivery to the patient.

Code Info

Lot Numbers: 313471, 313627 & 313696

Distribution

IL & OH distributors

Quantity

110 cases