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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CONTACT¿DETACH; CONTACT DETACH G29 60/8
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CONTACT¿DETACH; CONTACT DETACH G29 60/8 Back to Search Results
Lot Number 5136235
Medical Device Problem Code Detachment of Device or Device Component (2907)
Health Effect - Clinical Code Hyperglycemia (1905)
Type of Reportable Event Malfunction
Event or Problem Description
Unomedical reference number (b)(4).Event occurred in the united states.The patient reported that the he had issues unclipping and clipping the infusion set from the site.His blood glucose level was 500 mg/dl at the time of the event and he did not notice any damage when the package was first opened.No further information available.
 
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Brand Name
CONTACT¿DETACH
Common Device Name
CONTACT DETACH G29 60/8
MDR Report Key8460249
Report Number3003442380-2019-00751
Device Sequence Number11467789
Product Code FPA
UDI-Device Identifier05705244003378
UDI-Public05705244003378
Combination Product (Y/N)N
PMA/510(K) Number
K041545
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source distributor
Initial Reporter Occupation Other
Type of Report Initial
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
Operator of Device No Information
Device Lot Number5136235
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 07/19/2017
Initial Report FDA Received Date03/28/2019
Patient Sequence Number1
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