HUDSON POCKETPEAK,PEAK FLOW METER,UNIVERSAL RA 1801

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-10-26 for HUDSON POCKETPEAK,PEAK FLOW METER,UNIVERSAL RA 1801 manufactured by Teleflex Medical.

Event Text Entries

[29887488] Qn#(b)(4). The device sample was not returned for evaluation at the time of this report.
Patient Sequence No: 1, Text Type: N, H10


[29887489] The customer alleges that the blue indicator is loose giving an inaccurate reading. No patient injury reported.
Patient Sequence No: 1, Text Type: D, B5


[31822357] (b)(4). The sample was not returned for evaluation; therefore, the complaint could not be confirmed. If the sample is returned, a follow-up report will be submitted with investigation results.
Patient Sequence No: 1, Text Type: N, H10


[31822358] The customer alleges that the blue indicator is loose giving an inaccurate reading. No patient injury reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1044475-2015-00382
MDR Report Key5178635
Date Received2015-10-26
Date of Report2015-10-16
Date of Event2015-10-16
Date Mfgr Received2015-11-17
Date Added to Maude2015-10-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKATHARINE TARPLEY
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194334854
Manufacturer G1TELEFLEX MEDICAL
Manufacturer Street2917 WECK DRIVE
Manufacturer CityRESEARCH TRIANGLE PARK NC 27709
Manufacturer CountryUS
Manufacturer Postal Code27709
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHUDSON POCKETPEAK,PEAK FLOW METER,UNIVERSAL RA
Generic NamePEAK-FLOW METER
Product CodeBZH
Date Received2015-10-26
Catalog Number1801
OperatorLAY USER/PATIENT
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressRESEARCH TRIANGLE PARK NC


Patients

Patient NumberTreatmentOutcomeDate
10 2015-10-26

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.