MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2018-09-27 for PLACKERS MTH GD GNM 10CT manufactured by Ranir Llc.
[121990210]
Consumer called in asking if there was latex in the product. "i am allergic to if latex and had a reaction to it so i am just wondering if that's what it is!! "
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1825660-2018-00421 |
MDR Report Key | 7915478 |
Report Source | CONSUMER |
Date Received | 2018-09-27 |
Date of Report | 2018-09-27 |
Date of Event | 2018-09-14 |
Date Facility Aware | 2018-09-14 |
Date Mfgr Received | 2018-09-14 |
Date Added to Maude | 2018-09-27 |
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 | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | REBEKAH STENSKE |
Manufacturer Street | 4701 EAST PARIS AVE. SE |
Manufacturer City | GRAND RAPIDS MI 495125353 |
Manufacturer Country | US |
Manufacturer Postal | 495125353 |
Manufacturer Phone | 6166988880 |
Manufacturer G1 | RANIR LLC |
Manufacturer Street | 4701 EAST PARIS AVE. SE |
Manufacturer City | GRAND RAPIDS MI 495125353 |
Manufacturer Country | US |
Manufacturer Postal Code | 495125353 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PLACKERS MTH GD GNM 10CT |
Generic Name | MOUTHGUARD, OVER-THE-COUNTER |
Product Code | OBR |
Date Received | 2018-09-27 |
Model Number | MTH GD GNM 10CT |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | RANIR LLC |
Manufacturer Address | 4701 EAST PARIS AVE. SE GRAND RAPIDS MI |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-09-27 |