FDA.reportPublic FDA data

MAUDE MDR 9878182

MDR report key
9878182
Report number
9616091-2020-00015
Event key
0
Event type
3
Date received
2020-03-25
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
100
Health professional
3
Initial report to FDA
3
Event location
3

Manufacturer Contact#

Contact
MR. JASON FIEST
Address
ONE INVACARE WAY ELYRIA OH 44035 US
Phone
800-800-8003
Report source
M
Manufacturer link flag
Y

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
1POWER LIFT W/LOW BASE-PLUS 9153633519LIFT, PATIENT, NON-AC-POWEREDINVAMEX MANUFACTURINGFSANA:RPL450-1RPL450-1N R

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12020-03-2501. R

Event Narratives#

No narrative records found.