MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2020-03-29 for ULTRA FAST-FIX ASSEMBLY - CURVED 72201491 manufactured by Smith & Nephew, Inc..
[186231464]
It was reported that during a meniscal repair surgery the second anchor post deployment came out of the capsule. No patient injuries or significant delay reported. Back-up device was available to complete the surgery. Unknown if the t1 was removed from the capsule. All available information has been disclosed. If additional information should become available, a supplemental report will be submitted accordingly.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1219602-2020-00561 |
MDR Report Key | 9895105 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,O |
Date Received | 2020-03-29 |
Date of Report | 2020-03-29 |
Date of Event | 2020-02-28 |
Date Mfgr Received | 2020-03-03 |
Device Manufacturer Date | 2017-02-27 |
Date Added to Maude | 2020-03-29 |
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 | HOLLY TOPPING |
Manufacturer Street | 7000 WEST WILLIAM CANNON DRIVE |
Manufacturer City | AUSTIN TX 78735 |
Manufacturer Country | US |
Manufacturer Postal | 78735 |
Manufacturer Phone | 5123913905 |
Manufacturer G1 | SMITH & NEPHEW, INC. |
Manufacturer Street | 130 FORBES BOULEVARD |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal Code | 02048 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ULTRA FAST-FIX ASSEMBLY - CURVED |
Generic Name | SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE |
Product Code | GAT |
Date Received | 2020-03-29 |
Model Number | 72201491 |
Catalog Number | 72201491 |
Lot Number | 50649734 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITH & NEPHEW, INC. |
Manufacturer Address | 130 FORBES BOULEVARD MANSFIELD MA 02048 US 02048 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-29 |