THERABAND

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2016-06-17 for THERABAND manufactured by Hygenic Corporation.

Event Text Entries

[47646387] Every reasonalbe effort was made to obtain the device. Device was not returned. We are unable to confirm the deivce in question is our product.
Patient Sequence No: 1, Text Type: N, H10


[47646388] Patient was doing his daily physical therapy using a new theraband as instructed and prescribed by his personal physician. As he was pulling back the theraband broke and with the force sent his arm back to over a 90 degree angle and caused severe injury to his shoulder. He had to have surgery on his shoulder to repair the injury. The mri showed a complete rip to his shoulder.
Patient Sequence No: 1, Text Type: D, B5


[50077784] Every reasonable effort was made to obtain the device. Device was not returned. We are unable to confirm the device in question is our product. Follow up information: insurance claim was closed based on lack of evidence that it was a theraband
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1519375-2016-00002
MDR Report Key5732708
Report SourceCONSUMER
Date Received2016-06-17
Date of Report2016-06-16
Date of Event2013-07-10
Date Mfgr Received2015-03-17
Date Added to Maude2016-06-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationATTORNEY
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. LISA PIERO
Manufacturer Street1245 HOME AVE
Manufacturer CityAKRON OH 44310
Manufacturer CountryUS
Manufacturer Postal44310
Manufacturer Phone3306342238
Manufacturer G1HYGENIC CORPORATION
Manufacturer Street1245 HOME AVE
Manufacturer CityAKRON OH 44310
Manufacturer CountryUS
Manufacturer Postal Code44310
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTHERABAND
Generic NameEXERCISE BAND
Product CodeION
Date Received2016-06-17
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerHYGENIC CORPORATION
Manufacturer Address1245 HOME AVE AKRON OH 44310 US 44310


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2016-06-17

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