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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COVIDIEN CONTAINER 18 GAL CHEMO W SLIDE; CONTAINER, SHARPS

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COVIDIEN CONTAINER 18 GAL CHEMO W SLIDE; CONTAINER, SHARPS Back to Search Results
Model Number 8939
Device Problems Defective Component (2292); Detachment of Device or Device Component (2907)
Patient Problem No Patient Involvement (2645)
Event Date 09/20/2019
Event Type  malfunction  
Manufacturer Narrative
The incident sample has been requested but to date has not been received for evaluation.If the sample is received, or if additional information pertinent to the incident is obtained a follow-up report will be submitted.As part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product.
 
Event Description
The customer reported that when they received the containers the lids would not slide and would not stay attached.
 
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Brand Name
CONTAINER 18 GAL CHEMO W SLIDE
Type of Device
CONTAINER, SHARPS
Manufacturer (Section D)
COVIDIEN
815 tek drive
crystal lake IL 60039 9002
Manufacturer (Section G)
COVIDIEN
815 tek drive
crystal lake IL 60039 9002
Manufacturer Contact
jill saraiva
15 hampshire street
mansfield, MA 02048
5086183640
MDR Report Key9109653
MDR Text Key159866283
Report Number1424643-2019-00545
Device Sequence Number1
Product Code MMK
UDI-Device Identifier40884521022769
UDI-Public40884521022769
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,distri
Reporter Occupation Other
Type of Report Initial
Report Date 09/24/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator No Information
Device Model Number8939
Device Catalogue Number8939
Device Lot Number19H00563
Was Device Available for Evaluation? Yes
Initial Date Manufacturer Received 09/20/2019
Initial Date FDA Received09/24/2019
Type of Device Usage N
Patient Sequence Number1
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