HYPODERMIC NEEDLE-PRO WITH NEEDLE PROTECTION DEVICE G1741

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2015-04-21 for HYPODERMIC NEEDLE-PRO WITH NEEDLE PROTECTION DEVICE G1741 manufactured by Smiths Medical, Inc.

Event Text Entries

[18934311] A report was received that stated during an injection, the needle became detached from the syringe. The nurse removed the needle from the pt manually. No needle-stick took place. There was no pt or clinician injury reported.
Patient Sequence No: 1, Text Type: D, B5


[19067998] Customer has not yet returned the device to the mfr for device eval. When and if the device becomes available and is returned and evaluated, the mfr will file a follow up report detailing the results of the eval.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2183502-2015-00263
MDR Report Key4728042
Report Source08
Date Received2015-04-21
Date of Report2015-04-20
Date of Event2015-04-02
Date Facility Aware2015-04-02
Report Date2015-04-20
Date Reported to FDA2015-04-20
Date Mfgr Received2015-04-06
Date Added to Maude2015-06-08
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 ContactMICHELE SELIGA
Manufacturer Street1265 GREY FOX RD.
Manufacturer CityST. PAUL MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone6516287604
Manufacturer G1SMITHS MEDICAL, INC
Manufacturer Street10 BOWMAN DR
Manufacturer CityKEENE NH 03431
Manufacturer CountryUS
Manufacturer Postal Code03431
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHYPODERMIC NEEDLE-PRO WITH NEEDLE PROTECTION DEVICE
Generic NameNEEDLE, HYPODERMIC
Product CodeFMJ
Date Received2015-04-21
Model NumberNA
Catalog NumberG1741
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL, INC
Manufacturer AddressKEENE NH US


Patients

Patient NumberTreatmentOutcomeDate
10 2015-04-21

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