UNKNOWN_FRO_PRODUCT UNK_FRO

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-06-13 for UNKNOWN_FRO_PRODUCT UNK_FRO manufactured by Stryker Orthobiologics-malvern.

Event Text Entries

[47289925] Device is not available for evaluation. If additional information is received it will be reported on a supplemental report. Device was discarded prior to learning of the complaint.
Patient Sequence No: 1, Text Type: N, H10


[47289926] It was discovered that a patient reported he experienced pain and 3 follow up procedures, which he believes is due to the customer's medpor implant that he received seven years ago.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008010177-2016-00126
MDR Report Key5721227
Date Received2016-06-13
Date of Report2016-05-25
Date of Event2009-05-25
Date Mfgr Received2016-05-25
Date Added to Maude2016-06-13
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 ContactMR. KELLI DYKSTRA
Manufacturer StreetBOETZINGERSTR. 41
Manufacturer CityFREIBURG D-79111
Manufacturer PostalD-79111
Manufacturer Phone76145120
Manufacturer G1STRYKER ORTHOBIOLOGICS-MALVERN
Manufacturer Street45 GREAT VALLEY PARKWAY
Manufacturer CityMALVERN PA 19355
Manufacturer CountryUS
Manufacturer Postal Code19355
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameUNKNOWN_FRO_PRODUCT
Generic NameIMPLANT
Product CodeFWP
Date Received2016-06-13
Catalog NumberUNK_FRO
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ORTHOBIOLOGICS-MALVERN
Manufacturer Address45 GREAT VALLEY PARKWAY MALVERN PA 19355 US 19355


Patients

Patient NumberTreatmentOutcomeDate
10 2016-06-13

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