ACTIS BROACH SZ 8 2010-01-080 201001080

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-13 for ACTIS BROACH SZ 8 2010-01-080 201001080 manufactured by Depuy Ireland - 9616671.

MAUDE Entry Details

• Report Number: 1818910-2020-07846
• MDR Report Key: 9831230
• Report Source: COMPANY REPRESENTATIVE,HEALTH
• Date Received: 2020-03-13
• Date of Report: 2020-02-26
• Date of Event: 2020-02-26
• Date Mfgr Received: 2020-03-10
• Device Manufacturer Date: 2018-08-28
• Date Added to Maude: 2020-03-13
• 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
• Reporter Occupation: OTHER HEALTH CARE PROFESSIONAL
• Health Professional: 3
• Initial Report to FDA: 3
• Report to FDA: 3
• Event Location: 3
• Manufacturer Contact: KARA DITTY-BOVARD
• Manufacturer Street: 700 ORTHOPAEDIC DR.
• Manufacturer City: WARSAW IN 465810988
• Manufacturer Country: US
• Manufacturer Postal: 465810988
• Manufacturer Phone: 6107428552
• Manufacturer G1: DEPUY ORTHOPAEDICS, INC. 1818910
• Manufacturer Street: 700 ORTHOPAEDIC DR.
• Manufacturer City: WARSAW IN 465810988
• Manufacturer Country: US
• Manufacturer Postal Code: 465810988
• Single Use: 3
• Previous Use Code: 3
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: ACTIS BROACH SZ 8
• Generic Name: BROACHES
• Product Code: KWL
• Date Received: 2020-03-13
• Returned To Mfg: 2020-03-10
• Model Number: 2010-01-080
• Catalog Number: 201001080
• Lot Number: PG276856
• Operator: HEALTH PROFESSIONAL
• Device Availability: R
• Device Age: DA
• Device Eval'ed by Mfgr: R
• Device Sequence No: 1
• Device Event Key: 0
• Manufacturer: DEPUY IRELAND - 9616671
• Manufacturer Address: LOUGHBEG RINGASKIDDY CO. CORK EI

Patients

Patient Number	Treatment	Outcome	Date
1	0		2020-03-13