MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 99 report with the FDA on 2011-02-28 for TELEPORT 9044-00 manufactured by Interventional Spine, Inc..
        [16037980]
The surgeon released the final stage on the disposal teleport; unable to budge the "pull 2" button. Surgeon used a mallet and tapped it. The button finally worked and the case was completed.
 Patient Sequence No: 1, Text Type: D, B5
        [16093595]
Root cause: loose metallic debris: loose metallic debris was present because, the component was not properly deburred. Initially, it was determined, the event was not reportable. On a subsequent re-review, it was determined that this event should have been reported.
 Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2032499-2011-00025 | 
| MDR Report Key | 2045711 | 
| Report Source | 99 | 
| Date Received | 2011-02-28 | 
| Date of Report | 2009-06-03 | 
| Date Mfgr Received | 2009-06-03 | 
| Device Manufacturer Date | 2009-03-01 | 
| Date Added to Maude | 2012-02-10 | 
| 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 | 0 | 
| Event Location | 0 | 
| Manufacturer Street | 13700 ALTON PKWY, SUITE 160 | 
| Manufacturer City | IRVINE CA 92618 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 92618 | 
| Manufacturer Phone | 9494720006 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | TELEPORT | 
| Product Code | MRW | 
| Date Received | 2011-02-28 | 
| Model Number | 9044-00 | 
| Catalog Number | 9044-00 | 
| Lot Number | 020609-B | 
| Device Expiration Date | 2011-01-31 | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | Y | 
| Device Eval'ed by Mfgr | N | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | INTERVENTIONAL SPINE, INC. | 
| Manufacturer Address | IRVINE CA US | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2011-02-28 |