MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2017-01-25 for SINGLE USE INJECTOR NM-400U-0323 manufactured by Olympus Medical Systems Corp..
[65770747]
The subject device has not been returned to olympus medical systems corp. (omsc) for evaluation. The exact cause could not be conclusively determined. A supplemental report will be submitted, if additional and significant information becomes available at a later time.
Patient Sequence No: 1, Text Type: N, H10
[65770748]
During a colonoscopy, the needle tube of the subject device could not be retracted into the sheath. Therefore the doctor severed the sheath of the subject device. The intended procedure was completed with another device. No patient injury was reported.
Patient Sequence No: 1, Text Type: D, B5
[71006844]
This is a supplemental report for mfr report # 8010047-2017-00079 to provide additional information. The subject device was not returned to olympus medical systems corp. (omsc) for evaluation. As the result of checking the manufacturing record of the subject device, there was nothing abnormal found. The exact cause could not be conclusively determined, because the subject device was not returned. However, based on the similar cases in the past, the needle tube might be unable to retract into the sheath, because the sheath was kinked. The sheath might be kinked, because excessive load was applied to the sheath when the subject device was inserted into the endoscope, it was taken out from the sterile package, or it was checked before use. The instruction manual of the subject device warns; when inserting the instrument into the endoscope, retract the needle into the sheath, hold the instrument close to the biopsy valve, and keep it as straight as possible relative to the biopsy valve. Otherwise, the instrument could be damaged. Before use, inspect the insertion portion and the tube for damage.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 8010047-2017-00079 |
| MDR Report Key | 6278289 |
| Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
| Date Received | 2017-01-25 |
| Date of Event | 2017-01-04 |
| Date Mfgr Received | 2017-02-13 |
| Date Added to Maude | 2017-01-25 |
| 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 |
| Reporter Occupation | PHARMACIST |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR HIROKI MORIYAMA |
| Manufacturer Street | 2951 ISHIKAWA-CHO |
| Manufacturer City | HACHIOJI-SHI, TOKYO-TO |
| Manufacturer Country | US |
| Manufacturer Phone | 8142642517 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SINGLE USE INJECTOR |
| Generic Name | INJECTOR AND SHEATHSET |
| Product Code | FBK |
| Date Received | 2017-01-25 |
| Model Number | NM-400U-0323 |
| Lot Number | 66K |
| ID Number | 04953170382260 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | OLYMPUS MEDICAL SYSTEMS CORP. |
| Manufacturer Address | 2951 ISHIKAWA-CHO HACHIOJI-SHI, TOKYO-TO US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-01-25 |