SPECI-PAN DYND36600 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-02-05 for SPECI-PAN DYND36600 * manufactured by Medline Industries.

Event Text Entries

[16593900] The graduation markings on the speci-pan collection container are incorrect; the markings between the 100 and 200ml lines.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3611893
MDR Report Key3611893
Date Received2014-02-05
Date of Report2014-02-04
Date of Event2014-02-04
Report Date2014-02-04
Date Reported to FDA2014-02-05
Date Reported to Mfgr2014-02-07
Date Added to Maude2014-02-07
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameSPECI-PAN
Generic NameCONTAINER, SPECIMEN, NON-STERILE
Product CodeNNI
Date Received2014-02-05
Model NumberDYND36600
Catalog Number*
Lot Number2193 08314
ID Number*
Device AvailabilityY
Device Sequence No1
Device Event Key0
ManufacturerMEDLINE INDUSTRIES
Manufacturer AddressONE MEDLINE PL MUNDELEIN IL 60060 US 60060


Patients

Patient NumberTreatmentOutcomeDate
10 2014-02-05

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