MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-04 for PULSE OXIMETER MAX N manufactured by Stryker Sustainability Solutions, Inc..
[177594308]
We keep having multiple stryker neonatal/adult pulse oximeter sensors that are defective. The metal sensors are not showing in the holes. When this happens you can not get a reading or if you do its really low.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9665127 |
| MDR Report Key | 9665127 |
| Date Received | 2020-02-04 |
| Date of Report | 2019-12-05 |
| Date of Event | 2019-12-03 |
| Report Date | 2019-12-13 |
| Date Reported to FDA | 2019-12-13 |
| Date Reported to Mfgr | 2020-02-04 |
| Date Added to Maude | 2020-02-04 |
| 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 | OTHER HEALTH CARE PROFESSIONAL |
| 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 | PULSE OXIMETER |
| Generic Name | OXIMETER, REPROCESSED |
| Product Code | NLF |
| Date Received | 2020-02-04 |
| Model Number | MAX N |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER SUSTAINABILITY SOLUTIONS, INC. |
| Manufacturer Address | 5300 REGION COURT LAKELAND FL 33815 US 33815 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-02-04 |