MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-06-21 for CARDINAL SBA24LALCH manufactured by Cardinal Health 200 Llc.
[112177455]
Insufflation tubing in lap pack broken upon pack inspection.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5077996 |
| MDR Report Key | 7628873 |
| Date Received | 2018-06-21 |
| Date of Report | 2018-06-20 |
| Date of Event | 2018-06-19 |
| Date Added to Maude | 2018-06-22 |
| 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 | OTHER CAREGIVERS |
| 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 | CARDINAL |
| Generic Name | LAP PACK/ TUBING WITH FILTER INSUFLATION |
| Product Code | NKC |
| Date Received | 2018-06-21 |
| Catalog Number | SBA24LALCH |
| Lot Number | 915302 |
| 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 |
| Manufacturer Address | US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-06-21 |