MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-19 for MALYUGIN RING SYSTEM 7.0MM MAL-0002-1 manufactured by Microsurgical Technology, Inc..
[184072713]
Opened malyugin ring to sterile field; scrub tech handed instrument to surgeon; surgeon advanced instrument and noticed it was bent made contact with patient; removed instrument and another malyugin ring opened to sterile field to use on patient. Manufacturer response for malyugin ring, malyugin ring (per site reporter). Pending.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9853141 |
MDR Report Key | 9853141 |
Date Received | 2020-03-19 |
Date of Report | 2020-02-04 |
Date of Event | 2020-01-15 |
Report Date | 2020-02-04 |
Date Reported to FDA | 2020-02-04 |
Date Reported to Mfgr | 2020-03-19 |
Date Added to Maude | 2020-03-19 |
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 | RISK MANAGER |
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 | MALYUGIN RING SYSTEM 7.0MM |
Generic Name | CLIP, IRIS RETRACTOR |
Product Code | HOC |
Date Received | 2020-03-19 |
Returned To Mfg | 2020-01-28 |
Model Number | MAL-0002-1 |
Catalog Number | MAL-0002-1 |
Lot Number | 115311 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | 1 DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MICROSURGICAL TECHNOLOGY, INC. |
Manufacturer Address | 8415 154TH AVE., N.E. REDMOND WA 98052 US 98052 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-19 |