KLEENSPEC 590 SERIES DISP. VAGINAL SPECULA 59001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2012-06-27 for KLEENSPEC 590 SERIES DISP. VAGINAL SPECULA 59001 manufactured by Welch Allyn.

Event Text Entries

[17134842] Complainant stated that a medium sized disposable vaginal speculum broke when inserted into the pt. Complainant described the break on the bottom bill and a piece came off, leaving a sharp edge. The physician was able to remove the speculum and piece without incident or injury. The customer did not provide a pt identifier.
Patient Sequence No: 1, Text Type: D, B5


[17401614] This device has not been returned to welch allyn for evaluation. A follow-up report will be submitted when the evaluation is complete.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1316463-2012-00006
MDR Report Key2640418
Report Source05,06
Date Received2012-06-27
Date of Report2012-06-13
Date of Event2012-06-13
Date Mfgr Received2012-06-13
Date Added to Maude2012-10-17
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 FDA0
Event Location0
Manufacturer ContactPEARLY BHAMBRI, DIRECTOR
Manufacturer Street4341 STATE STREET ROAD P.O. BOX 220
Manufacturer CitySKANEATELES FALLS NY 131530220
Manufacturer CountryUS
Manufacturer Postal131530220
Manufacturer Phone3156852568
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKLEENSPEC 590 SERIES DISP. VAGINAL SPECULA
Product CodeHIB
Date Received2012-06-27
Model Number59001
Catalog Number59001
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerWELCH ALLYN
Manufacturer Address4341 STATE STREET ROAD SKANEATELES FALLS NY 13153 US 13153


Patients

Patient NumberTreatmentOutcomeDate
10 2012-06-27

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