MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-08-23 for CARPUJECT HOLDER manufactured by Hospira.
[83541754]
Nurse pulled morphine 2mg injection and it was sealed (not tampered with) but discovered it only contained 1mg. Provider was also in the room when the nurse pulled opioid. Charged nurse was contacted and event was recorded to hospital reporting system. Morphine 2mg/ml, dose or amount: 1 mg, frequency: prn, route: intravenous, for 2 days.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5071755 |
| MDR Report Key | 6812864 |
| Date Received | 2017-08-23 |
| Date of Report | 2017-08-21 |
| Date of Event | 2017-08-21 |
| Date Added to Maude | 2017-08-23 |
| 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 | UNKNOWN |
| 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 | CARPUJECT HOLDER |
| Generic Name | ADAPTER, HOLDER, SYRINGE |
| Product Code | IQG |
| Date Received | 2017-08-23 |
| Lot Number | 71515LL |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | HOSPIRA |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-08-23 |