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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: VENTLAB LLC. AIRFLOW; RESUS BAG

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VENTLAB LLC. AIRFLOW; RESUS BAG Back to Search Results
Model Number AF1140MB
Device Problems Device Issue (2379); Separation Failure (2547)
Patient Problems Not Applicable (3189); Missing Value Reason (3192)
Event Date 08/29/2016
Event Type  malfunction  
Manufacturer Narrative
An extensive and thorough investigation was performed by the engineering team that concluded the root cause for this problem is the fact that the patient port and the mask are made out of similar base materials resulting in an undesirably high coefficient of friction between the two parts.Steps have been taken to implement a material combination with a lower coefficient of friction that significantly reduces the effort required to remove the mask from the patient valve.
 
Event Description
The customer alleges "patient valve on the bag broke." no other details were provided.
 
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Brand Name
AIRFLOW
Type of Device
RESUS BAG
Manufacturer (Section D)
VENTLAB LLC.
2710 northridgedr. suite a
grand rapids MI 49544
Manufacturer (Section G)
VENTLAB LLC.
2710 northridgedr. suite a
grand rapids MI 49544
Manufacturer Contact
carrie fortuna
2710 northridge dr. suite a
grand rapids, MI 49544
6162598350
MDR Report Key5984150
MDR Text Key55839006
Report Number2246980-2016-00050
Device Sequence Number1
Product Code BTM
Combination Product (y/n)N
PMA/PMN Number
K012842
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type user facility
Reporter Occupation Other
Type of Report Initial
Report Date 09/28/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/28/2016
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator No Information
Device Model NumberAF1140MB
Device Lot Number305242
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Device Manufactured05/01/2016
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age67 YR
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