ANDERSON AN10-S (AN10.11)

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2010-01-13 for ANDERSON AN10-S (AN10.11) manufactured by Andersen Products, Inc..

Event Text Entries

[22103759] Pt was incubated with an an10. 11 and the stylet broke from the tube when it was trying to be removed. The tube was then safely removed from the pt.
Patient Sequence No: 1, Text Type: D, B5


[22118589] Results could not be duplicated with sample tested.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1053825-2010-00001
MDR Report Key1586334
Report Source06
Date Received2010-01-13
Date of Report2010-01-13
Date of Event2009-12-15
Date Facility Aware2009-12-15
Report Date2010-01-13
Date Reported to FDA2010-01-13
Date Reported to Mfgr2009-12-16
Date Mfgr Received2009-12-15
Device Manufacturer Date2009-04-02
Date Added to Maude2010-10-19
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 Street3202 CAROLINE DR., HEALTH SCIENCE PARK
Manufacturer CityHAW RIVER NC 27258
Manufacturer CountryUS
Manufacturer Postal27258
Manufacturer Phone3363763000
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameANDERSON AN10-S (AN10.11)
Generic NameAN10-S
Product CodeBSS
Date Received2010-01-13
Model NumberAN10-S
Catalog NumberAN10.11
Lot Number290073
ID NumberNA
Device Expiration Date2014-04-02
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age8 MO
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerANDERSEN PRODUCTS, INC.
Manufacturer AddressHAW RIVER NC US


Patients

Patient NumberTreatmentOutcomeDate
10 2010-01-13

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