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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CARDINAL HEALTH UNKNOWN ENTERAL ACCESS; TUBES, GASTROINTESTINAL (AND ACCESSORIES)

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CARDINAL HEALTH UNKNOWN ENTERAL ACCESS; TUBES, GASTROINTESTINAL (AND ACCESSORIES) Back to Search Results
Model Number UNKNOWN ENTERAL ACCESS
Device Problem Obstruction of Flow (2423)
Patient Problem Insufficient Information (4580)
Event Type  malfunction  
Manufacturer Narrative
This complaint was received via an anonymous clinical study.Sample analysis could not be performed since samples were not provided for evaluation.This complaint will be used for trending and post market analysis.
 
Event Description
Per a post market clinical survey, the customer observed a clogged tube with the use of a neonatal/pediatric feeding tube.The customer stated there was a possible device relationship.This information was received via an anonymous post market clinical study; therefore, the customer information is unknown and no further information will be provided.
 
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Brand Name
UNKNOWN ENTERAL ACCESS
Type of Device
TUBES, GASTROINTESTINAL (AND ACCESSORIES)
Manufacturer (Section D)
CARDINAL HEALTH
777 west street
mansfield MA 02048
Manufacturer (Section G)
CARDINAL HEALTH
calle 9 sur no. 125 cuidad ind
tijuana 22500
MX   22500
Manufacturer Contact
jill saraiva
777 west street
mansfield, MA 02048
5086183640
MDR Report Key16490478
MDR Text Key311291695
Report Number9612030-2023-03611
Device Sequence Number1
Product Code KNT
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Other
Reporter Occupation Other
Type of Report Initial
Report Date 03/06/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/06/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model NumberUNKNOWN ENTERAL ACCESS
Device Catalogue NumberUNKNOWN ENTERAL ACCESS
Was Device Available for Evaluation? No
Date Manufacturer Received02/15/2023
Is the Device Single Use? No
Type of Device Usage A
Patient Sequence Number1
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