MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-06 for VOLU-FEED 00180 manufactured by Abbott Nutrition.
[173713398]
Volu-feed bottles and caps have dates that are confusing to user. Not clearly identified as either an expiration date or a manufacture date.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9551226 |
| MDR Report Key | 9551226 |
| Date Received | 2020-01-06 |
| Date of Report | 2019-12-26 |
| Date of Event | 2019-12-19 |
| Report Date | 2019-12-26 |
| Date Reported to FDA | 2019-12-26 |
| Date Reported to Mfgr | 2020-01-06 |
| Date Added to Maude | 2020-01-06 |
| Event Key | 0 |
| Report Source Code | User Facility 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 | RISK MANAGER |
| 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 | 3 |
| Brand Name | VOLU-FEED |
| Generic Name | NIPPLE, LAMBS FEEDING |
| Product Code | FNN |
| Date Received | 2020-01-06 |
| Model Number | 00180 |
| Device Availability | * |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ABBOTT NUTRITION |
| Manufacturer Address | 2141 SOUTHWEST BLVD GROVE CITY OH 43123 US 43123 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-01-06 |