MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-24 for NOVAPLUS INSTANT HOT PACK V11443-012B manufactured by Cardinal Health 200, Llc.
[181136285]
Hot pack exploded when staff member attempted to activate. Contents of hot pack made contact with clothing of two staff members. No staff or pt harm.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5093233 |
MDR Report Key | 9750346 |
Date Received | 2020-02-24 |
Date of Report | 2020-02-10 |
Date of Event | 2020-02-09 |
Date Added to Maude | 2020-02-25 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 0 |
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 | NOVAPLUS INSTANT HOT PACK |
Generic Name | PACK, HOT OR COLD, DISPOSABLE |
Product Code | IMD |
Date Received | 2020-02-24 |
Catalog Number | V11443-012B |
Lot Number | V0A101 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | I |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CARDINAL HEALTH 200, LLC |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-24 |