CONFORM MEMBRANE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-07-21 for CONFORM MEMBRANE manufactured by Collagen Matrix, Inc..

Event Text Entries

[80901392] Manufacturer could not confirm the complaint following several unsuccessful attempts to obtain additional product information (ie. Udi, product reference number, lot number). The manufacturer is currently unable to conduct a complete assessment based on the limited information provided. Should clinically relevant information become available, a reassessment will be performed based on the information provided.
Patient Sequence No: 1, Text Type: N, H10


[80901393] It was reported by the distributor that a clinician at an undisclosed military base implanted a conform membrane which was past its expiration/use by date. No additional information pertaining to product identification/traceability or patient outcome was received by the manufacturer.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2249852-2017-00006
MDR Report Key6734624
Date Received2017-07-21
Date of Report2017-03-22
Date Mfgr Received2017-02-13
Date Added to Maude2017-07-21
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMS. GLORIA ZUCLICH
Manufacturer Street15 THORNTON ROAD
Manufacturer CityOAKLAND NJ 07436
Manufacturer CountryUS
Manufacturer Postal07436
Manufacturer Phone2014051477
Manufacturer G1COLLAGEN MATRIX, INC.
Manufacturer Street15 THORNTON ROAD
Manufacturer CityOAKLAND NJ 07436
Manufacturer CountryUS
Manufacturer Postal Code07436
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCONFORM MEMBRANE
Generic NameCOLLAGEN DENTAL MEMBRANE - CONFORMABLE II
Product CodeNPL
Date Received2017-07-21
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOLLAGEN MATRIX, INC.
Manufacturer Address15 THORNTON ROAD OAKLAND NJ 07436 US 07436


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-07-21

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