BULK SURG PATTIE 1X1 24-5407

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-15 for BULK SURG PATTIE 1X1 24-5407 manufactured by Codman & Shurtleff, Inc..

Event Text Entries

[136894267] (b)(4). Complaint sample was not returned to codman; therefore, an evaluation of the device could not be performed. A review of manufacturing records found no discrepancies when the device was released. The cause(s) of the difficulty reported by the customer could not be determined. If the complaint sample becomes available, this complaint will be reopened, and the respective evaluation performed. Trends will be monitored for this or similar complaints. At present, we consider this complaint to be closed.
Patient Sequence No: 1, Text Type: N, H10


[136894268] As reported, a package of neuro sponges were dirty and unusable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1226348-2019-10110
MDR Report Key8345555
Date Received2019-02-15
Date of Report2019-01-25
Date of Event2019-01-22
Date Mfgr Received2019-02-28
Device Manufacturer Date2018-09-07
Date Added to Maude2019-02-15
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 ContactKAREN ANIGBO
Manufacturer Street11 CABOT BOULEVARD
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone7819715608
Manufacturer G1CODMAN & SHURTLEFF, INC.
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal Code02767
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBULK SURG PATTIE 1X1
Generic NamePATTIE, COTTONOID
Product CodeHBA
Date Received2019-02-15
Returned To Mfg2019-02-26
Catalog Number24-5407
Lot NumberJ0454H
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCODMAN & SHURTLEFF, INC.
Manufacturer Address325 PARAMOUNT DRIVE RAYNHAM MA 02767 US 02767


Patients

Patient NumberTreatmentOutcomeDate
10 2019-02-15

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