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

MAUDE Adverse Event Report: EXCELSIOR MEDICAL, LLC; SYRINGE, 10ML SALINE IN 10ML

  • 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
 

EXCELSIOR MEDICAL, LLC; SYRINGE, 10ML SALINE IN 10ML Back to Search Results
Catalog Number EMZE010001
Device Problem Material Integrity Problem (2978)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 09/22/2020
Event Type  malfunction  
Event Description
It was reported that the syringe "wings" are "breaking while pushing the plunger in".
 
Manufacturer Narrative
It was reported that the syringe "wings" are "breaking while pushing the plunger in".To date, no information has been received to indicate that a user or a patient experienced a death, serious injury, medical intervention, follow-up care, or other adverse health impact associated with the reported problem/issue.Due to the reported problem/issue, and in an abundance of caution, this medwatch is being filed.If additional relevant information becomes available a supplemental medwatch will be filed.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Type of Device
SYRINGE, 10ML SALINE IN 10ML
Manufacturer (Section D)
EXCELSIOR MEDICAL, LLC
1933 heck avenue
neptune NJ 07753 4428
Manufacturer Contact
danielle tognocchi
three lakes drive
northfield, IL 60093
MDR Report Key18764175
MDR Text Key336884177
Report Number2027791-2024-00004
Device Sequence Number1
Product Code NGT
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Other
Type of Report Initial
Report Date 02/22/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/22/2024
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Catalogue NumberEMZE010001
Device Lot Number3138717
Was Device Available for Evaluation? No
Date Manufacturer Received09/22/2020
Was Device Evaluated by Manufacturer? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
Patient Outcome(s) Other;
-
-