Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ENFIT INJECTABLE SYRINGE; ENTERAL SYRINGES WITH ENTERAL SPECIFIC CONNECTORS
  • 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
 

ENFIT INJECTABLE SYRINGE; ENTERAL SYRINGES WITH ENTERAL SPECIFIC CONNECTORS Back to Search Results
Patient Problem Insufficient Information (4580)
Event Type  Other  
Event Description
Parents unable to administer medications or measure medication appropriately.(b)(4).Submission id: (b)(4).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
ENFIT INJECTABLE SYRINGE
Type of Device
ENTERAL SYRINGES WITH ENTERAL SPECIFIC CONNECTORS
MDR Report Key18065083
MDR Text Key327596582
Report NumberMW5147709
Device Sequence Number1
Product Code PNR
Combination Product (y/n)Y
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Unknown
Type of Report Initial
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received11/01/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Patient Sequence Number1
-
-