• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: FERRING PHARMACEUTICALS EUFLEXXA INJ 10MG/ML ACID, HYALURONIC INTRAARTICULAR

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

FERRING PHARMACEUTICALS EUFLEXXA INJ 10MG/ML ACID, HYALURONIC INTRAARTICULAR Back to Search Results
Device Problem Manufacturing, Packaging or Shipping Problem (2975)
Patient Problem Missed Dose (2561)
Event Date 12/13/2018
Event Type  Injury  
Event Description
The euflexxa order is lost in the mail. It did not make it to the doctor's office. As a result, the patient missed their scheduled injection. A replacement is being sent. The pt has spoken with the doctor. They will reschedule. Dates of use: (b)(6) 2018 - present.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameEUFLEXXA INJ 10MG/ML
Type of DeviceACID, HYALURONIC INTRAARTICULAR
Manufacturer (Section D)
FERRING PHARMACEUTICALS
MDR Report Key8194353
MDR Text Key131545875
Report NumberMW5082526
Device Sequence Number1
Product Code MOZ
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Pharmacist
Type of Report Initial
Report Date 12/13/2018
1 Device was Involved in the Event
0 Patients were Involved in the Event:
Date FDA Received12/21/2018
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA?
Event Location No Information
Was Device Evaluated by Manufacturer?
Is the Device Single Use?
Is This a Reprocessed and Reused Single-Use Device?
Type of Device Usage

-
-