MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-04-17 for PLACKERS MTH GD GNM MTH GD GNM 10CT manufactured by Ranir Llc.
[142516009]
Consumer called and asked if people have ever swallowed the grind no more guard because she can't find it in her room this morning. Consumer was not able to confirm whether or not she swallowed the guard.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1825660-2019-00539 |
MDR Report Key | 8524725 |
Date Received | 2019-04-17 |
Date of Report | 2019-04-17 |
Date of Event | 2019-04-02 |
Date Facility Aware | 2019-04-02 |
Date Mfgr Received | 2019-04-02 |
Date Added to Maude | 2019-04-17 |
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 | 0 |
Brand Name | PLACKERS MTH GD GNM |
Generic Name | MOUTHGUARD, OVER-THE-COUNTER |
Product Code | OBR |
Date Received | 2019-04-17 |
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 495125353 US 495125353 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-04-17 |