BAG SET, 1200ML, ENFITCONNECTOR INF1200-A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2018-06-15 for BAG SET, 1200ML, ENFITCONNECTOR INF1200-A manufactured by Moog Medical Devices Group.

Event Text Entries

[112039207] The device was not returned to mmdg for evaluation. Because it was not returned, mmdg has been unable to investigate or confirm the complaint.
Patient Sequence No: 1, Text Type: N, H10


[112039208] The initial reporter states that the "formula gets stuck where the connection is". Mmdg was advised at the time of the complaint that no other information or clarification regarding the complaint was available. (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1722139-2018-00167
MDR Report Key7607532
Report SourceUSER FACILITY
Date Received2018-06-15
Date of Report2018-05-21
Date of Event2018-05-21
Date Mfgr Received2018-05-21
Date Added to Maude2018-06-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKRISTIN HARDESTY
Manufacturer Street4314 ZEVEX PARK LANE
Manufacturer CitySALT LAKE CITY UT 84123
Manufacturer CountryUS
Manufacturer Postal84123
Manufacturer Phone8012641001
Manufacturer G1MOOG MEDICAL DEVICES GROUP, SRL
Manufacturer StreetCOYOL FREE ZONE AND BUSINESS PARK
Manufacturer CityALAJUELA, SAN JOSE 20113
Manufacturer CountryCS
Manufacturer Postal Code20113
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBAG SET, 1200ML, ENFITCONNECTOR
Generic NameENTERAL FEEDING SET
Product CodePIO
Date Received2018-06-15
Model NumberINF1200-A
Catalog NumberINF1200-A
Lot NumberCF1725709
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMOOG MEDICAL DEVICES GROUP
Manufacturer Address4314 ZEVEX PARK LANE SALT LAKE CITY UT 84123 US 84123


Patients

Patient NumberTreatmentOutcomeDate
10 2018-06-15

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.