MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-20 for VULLI 2 PACK VANILLA FLAVORED RING TEETHER manufactured by Unk.
[117960147]
The vulli 2 pack vanilla flavored ring teethers material breaks down and breaks off in small pieces. Colors may vary. Document number:(b)(4).
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5079249 |
MDR Report Key | 7801586 |
Date Received | 2018-08-20 |
Date of Report | 2018-08-01 |
Date of Event | 2018-07-24 |
Date Added to Maude | 2018-08-21 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | PATIENT |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | VULLI 2 PACK VANILLA FLAVORED RING TEETHER |
Generic Name | VULLI 2 PACK VANILLA FLAVORED RING TEETHER |
Product Code | MEF |
Date Received | 2018-08-20 |
Device Availability | Y |
Device Eval'ed by Mfgr | I |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | UNK |
Manufacturer Address | UNK UNK |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-08-20 |