LEECHES BM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2017-07-14 for LEECHES BM manufactured by Ricarimpex.

Event Text Entries

[80051555] Manufacturing records including acceptance testing results were checked and found to be conforming to specifications upon release. Return of the lot has been requested. Device not yet available. If additional information becomes available, a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[80051556] During routine testing of leeches for antibiotic resistance by the user (healthcare facility) at the moment of receipt and after several days of storage, the user detected: trimethoprim/sulfamethoxazole-resistant aeromonas hydrophila at receipt on (b)(6) 2017 (shipping water). Lot conforming to specifications when retested on (b)(6) 2017 (hospital storage water).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3009106257-2017-00002
MDR Report Key6713647
Report SourceUSER FACILITY
Date Received2017-07-14
Date of Report2017-10-06
Date Mfgr Received2017-09-08
Device Manufacturer Date2017-03-27
Date Added to Maude2017-07-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPHARMACIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactSONIA BARBE
Manufacturer Street245, AVENUE DE SAINT MEDARD
Manufacturer CityEYSINES, AQUITAINE 33320
Manufacturer CountryFR
Manufacturer Postal33320
Manufacturer G1RICARIMPEX
Manufacturer Street245 AVENUE DE SAINT MEDARD
Manufacturer CityEYSINES, AQUITAINE 33320
Manufacturer CountryFR
Manufacturer Postal Code33320
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLEECHES
Generic NameLEECHES HIRUDO MEDICINALIS
Product CodeNRN
Date Received2017-07-14
Model NumberBM
Lot Number17/270/B
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerRICARIMPEX
Manufacturer Address245, AVENUE DE SAINT MEDARD EYSINES, AQUITAINE 33320 FR 33320


Patients

Patient NumberTreatmentOutcomeDate
10 2017-07-14

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