MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-04-26 for CUB PEDIATRIC CRIB- HYD BASE FL19H manufactured by Stryker Medical-kalamazoo.
        [143315385]
This mdr is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program. The devices were evaluated in the field and the issue was confirmed; there were broken/damaged components. The devices were repaired and returned. There was no remedial action taken. This device is not labeled for single use.
 Patient Sequence No: 1, Text Type: N, H10
        [143315386]
This report summarizes 
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0001831750-2019-00538 | 
| MDR Report Key | 8557517 | 
| Report Source | COMPANY REPRESENTATIVE | 
| Date Received | 2019-04-26 | 
| Date of Report | 2019-04-26 | 
| Date of Event | 2019-01-01 | 
| Date Mfgr Received | 2019-04-01 | 
| Date Added to Maude | 2019-04-26 | 
| Event Key | 0 | 
| Report Source Code | Manufacturer report | 
| Manufacturer Link | Y | 
| Number of Patients in Event | 0 | 
| Adverse Event Flag | 3 | 
| Product Problem Flag | 3 | 
| Reprocessed and Reused Flag | 3 | 
| Health Professional | 3 | 
| Initial Report to FDA | 3 | 
| Report to FDA | 3 | 
| Event Location | 3 | 
| Manufacturer Contact | MR. MARY KLAVER | 
| Manufacturer Street | 3800 EAST CENTRE AVENUE | 
| Manufacturer City | PORTAGE MI 49002 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 49002 | 
| Manufacturer Phone | 2693292100 | 
| Manufacturer G1 | STRYKER MEDICAL-KALAMAZOO | 
| Manufacturer Street | 3800 EAST CENTRE AVENUE | 
| Manufacturer City | PORTAGE MI 49002 | 
| Manufacturer Country | US | 
| Manufacturer Postal Code | 49002 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | CUB PEDIATRIC CRIB- HYD BASE | 
| Generic Name | BED, PEDIATRIC OPEN HOSPITAL | 
| Product Code | FMS | 
| Date Received | 2019-04-26 | 
| Catalog Number | FL19H | 
| Device Availability | Y | 
| Device Eval'ed by Mfgr | Y | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | STRYKER MEDICAL-KALAMAZOO | 
| Manufacturer Address | 3800 EAST CENTRE AVENUE PORTAGE MI 49002 US 49002 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 2019-04-26 |