SUPER QA+ #2 PAN CP-2 *EA 212135

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2020-02-13 for SUPER QA+ #2 PAN CP-2 *EA 212135 manufactured by Depuy Mitek Llc Us.

Event Text Entries

[179274574] (b)(4). If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. (b)(4). The expiration date is unknown. This is report 3 of 4.
Patient Sequence No: 1, Text Type: N, H10


[179274575] It was reported by the affiliate by customer's email that during an unknown procedure the suture material of the super qa+ #2 pan cp-2 *ea torn despite the experienced pulling and knowledge of the implant. No patient consequence and no surgical delay was reported. Additional information: adequate supply of the knee extensor was not possible.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1221934-2020-00555
MDR Report Key9706048
Report SourceFOREIGN,HEALTH PROFESSIONAL,O
Date Received2020-02-13
Date of Report2020-02-04
Date of Event2020-01-09
Date Mfgr Received2020-02-24
Date Added to Maude2020-02-13
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 ContactKARA DITTY-BOVARD
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal02767
Manufacturer Phone6103142063
Manufacturer G1MEDOS INT MITEK
Manufacturer StreetCHEMIN BLANC 38
Manufacturer CityLE LOCLE 02400
Manufacturer CountrySZ
Manufacturer Postal Code02400
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSUPER QA+ #2 PAN CP-2 *EA
Generic NameSOFT-TISSUE ANCHOR, BIOABSORBABLE
Product CodeJDR
Date Received2020-02-13
Model Number212135
Catalog Number212135
Lot Number5L80121
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY MITEK LLC US
Manufacturer Address325 PARAMOUNT DRIVE RAYNHAM MA 02767 US 02767


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-13

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