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..
[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
Report Number | 2249852-2017-00006 |
MDR Report Key | 6734624 |
Date Received | 2017-07-21 |
Date of Report | 2017-03-22 |
Date Mfgr Received | 2017-02-13 |
Date Added to Maude | 2017-07-21 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. GLORIA ZUCLICH |
Manufacturer Street | 15 THORNTON ROAD |
Manufacturer City | OAKLAND NJ 07436 |
Manufacturer Country | US |
Manufacturer Postal | 07436 |
Manufacturer Phone | 2014051477 |
Manufacturer G1 | COLLAGEN MATRIX, INC. |
Manufacturer Street | 15 THORNTON ROAD |
Manufacturer City | OAKLAND NJ 07436 |
Manufacturer Country | US |
Manufacturer Postal Code | 07436 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | CONFORM MEMBRANE |
Generic Name | COLLAGEN DENTAL MEMBRANE - CONFORMABLE II |
Product Code | NPL |
Date Received | 2017-07-21 |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COLLAGEN MATRIX, INC. |
Manufacturer Address | 15 THORNTON ROAD OAKLAND NJ 07436 US 07436 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2017-07-21 |