MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2000-02-25 for HOLLISTER CORD CLAMP CLIPPER * 9441 manufactured by Hollister, Inc..
[178294]
Nurse attempting to remove a cord clamp from pt with a cord clamp remover. The blade (razor) dislodged from the clamp remover and stuck in the cord clamp. Nurse cut right thumb when protected baby's abdomen from the razor blade.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1018263 |
| MDR Report Key | 266263 |
| Date Received | 2000-02-25 |
| Date of Report | 2000-02-24 |
| Date of Event | 1999-12-21 |
| Date Added to Maude | 2000-03-02 |
| 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 | 0 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | HOLLISTER CORD CLAMP CLIPPER |
| Generic Name | CORD CLAMP CLIPPER |
| Product Code | HFW |
| Date Received | 2000-02-25 |
| Model Number | * |
| Catalog Number | 9441 |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 257764 |
| Manufacturer | HOLLISTER, INC. |
| Manufacturer Address | 2000 HOLLISTER DR. LIBERTYVILLE IL 60048 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2000-02-25 |