REILL TENDON STRIPPER #3 D6MM 400MM FO930R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-01-26 for REILL TENDON STRIPPER #3 D6MM 400MM FO930R manufactured by Aesculap Ag.

Event Text Entries

[37612315] (b)(4). Manufacturing site evaluation: on-going.
Patient Sequence No: 1, Text Type: N, H10


[37612316] Country of complaint: (b)(6). The surgeon used a open stripper, but it proved difficult to use and the results were inconclusive.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2916714-2016-00049
MDR Report Key5391779
Date Received2016-01-26
Date of Report2016-01-26
Date of Event2015-12-21
Date Facility Aware2016-01-20
Date Mfgr Received2015-12-21
Date Added to Maude2016-01-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
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 NameREILL TENDON STRIPPER #3 D6MM 400MM
Generic NameSPECIAL PRODUCTS FOR HAND / FOOT SU
Product CodeHRT
Date Received2016-01-26
Model NumberFO930R
Catalog NumberFO930R
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-01-26

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