CURITY 44101-

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-06-01 for CURITY 44101- manufactured by Covidien.

Event Text Entries

[110224392] 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. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[110224393] The customer reported the adhesive was stickier than normal. It wasn't coming out easily. When the patient removed it finally, it discolored her skin and left a dark patch on the skin which came in contact with the adhesive.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1282497-2018-00441
MDR Report Key7561064
Date Received2018-06-01
Date of Report2018-06-01
Date of Event2018-05-14
Date Mfgr Received2018-05-24
Date Added to Maude2018-06-01
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactEDWARD ALMEIDA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524151
Manufacturer G1COVIDIEN
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal Code02048
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCURITY
Generic NameTAPE AND BANDAGE, ADHESIVE
Product CodeFQM
Date Received2018-06-01
Model Number44101-
Catalog Number44101-
Lot NumberB1710182
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address15 HAMPSHIRE STREET MANSFIELD MA 02048 US 02048


Patients

Patient NumberTreatmentOutcomeDate
10 2018-06-01

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