SENSATION MICRSCIS S/S BAY STR 120/245MM FM124R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-05-27 for SENSATION MICRSCIS S/S BAY STR 120/245MM FM124R manufactured by Aesculap Ag.

Event Text Entries

[46779906] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[46779907] Country of complaint: (b)(6). Staff member in hospital injured by protruding instrument from outer box. Instrument had breached inner box packaging and pierced outer shipping box.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2916714-2016-00438
MDR Report Key5685186
Date Received2016-05-27
Date of Report2018-12-06
Date Facility Aware2016-01-16
Date Mfgr Received2016-01-16
Device Manufacturer Date2016-02-10
Date Added to Maude2016-05-27
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 ContactMS. NICOLE BROYLES
Manufacturer Street615 LAMBERT POINTE DRIVE
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3145515988
Manufacturer G1AESCULAP AG
Manufacturer StreetPO BOX 40
Manufacturer CityTUTTLINGEN, 78501
Manufacturer CountryGM
Manufacturer Postal Code78501
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSENSATION MICRSCIS S/S BAY STR 120/245MM
Generic NameSCISSOR
Product CodeHRR
Date Received2016-05-27
Returned To Mfg2016-05-31
Model NumberFM124R
Catalog NumberFM124R
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-05-27

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