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 2020-02-13 for SUPER QA+ #2 PAN CP-2 *EA 212135 manufactured by Depuy Mitek Llc Us.
[179274574]
(b)(4). If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. (b)(4). The expiration date is unknown. This is report 3 of 4.
Patient Sequence No: 1, Text Type: N, H10
[179274575]
It was reported by the affiliate by customer's email that during an unknown procedure the suture material of the super qa+ #2 pan cp-2 *ea torn despite the experienced pulling and knowledge of the implant. No patient consequence and no surgical delay was reported. Additional information: adequate supply of the knee extensor was not possible.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1221934-2020-00555 |
MDR Report Key | 9706048 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,O |
Date Received | 2020-02-13 |
Date of Report | 2020-02-04 |
Date of Event | 2020-01-09 |
Date Mfgr Received | 2020-02-24 |
Date Added to Maude | 2020-02-13 |
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 | KARA DITTY-BOVARD |
Manufacturer Street | 325 PARAMOUNT DRIVE |
Manufacturer City | RAYNHAM MA 02767 |
Manufacturer Country | US |
Manufacturer Postal | 02767 |
Manufacturer Phone | 6103142063 |
Manufacturer G1 | MEDOS INT MITEK |
Manufacturer Street | CHEMIN BLANC 38 |
Manufacturer City | LE LOCLE 02400 |
Manufacturer Country | SZ |
Manufacturer Postal Code | 02400 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SUPER QA+ #2 PAN CP-2 *EA |
Generic Name | SOFT-TISSUE ANCHOR, BIOABSORBABLE |
Product Code | JDR |
Date Received | 2020-02-13 |
Model Number | 212135 |
Catalog Number | 212135 |
Lot Number | 5L80121 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY MITEK LLC US |
Manufacturer Address | 325 PARAMOUNT DRIVE RAYNHAM MA 02767 US 02767 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-13 |