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Recall Observatory FDA recall evidence

Device product

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK 5, BAG RESERVOIR, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1116PD5

Z-2151-2018

May 24, 2018

Class II

Product summary

Firm
Sun Med, LLC
Event
Event 80201
Status
Terminated
Classification
Class II
Quantity
55 cases
Official record key
device-enforcement:Z-2151-2018

Official wording

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 information: Lot Numbers: 313326, 313436 & 313049

Distribution pattern: IL & OH distributors

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.