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

MAUDE Adverse Event Report: MHC MEDICAL PRODCUTS, LLC. MVP VET SYRINGES; INSULIN SYRINGES

  • 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
 

MHC MEDICAL PRODCUTS, LLC. MVP VET SYRINGES; INSULIN SYRINGES Back to Search Results
Catalog Number 819550
Device Problems Component Missing (2306); Material Deformation (2976); Material Twisted/Bent (2981)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 11/05/2018
Event Type  malfunction  
Event Description
Bent syringes and missing needles.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
MVP VET SYRINGES
Type of Device
INSULIN SYRINGES
Manufacturer (Section D)
MHC MEDICAL PRODCUTS, LLC.
8695 seward road
fairfield OH 45011
Manufacturer (Section G)
MHC MEDICAL PRODCUTS, LLC.
8695 seward road
fairfield OH 45011
Manufacturer Contact
jennifer seiple
8695 seward road
fairfield, OH 45011
MDR Report Key8140694
MDR Text Key129581553
Report Number3005798905-2018-02764
Device Sequence Number1
Product Code FMF
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K102178
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Reporter Occupation Non-Healthcare Professional
Remedial Action Replace
Type of Report Initial
Report Date 11/05/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/07/2018
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Catalogue Number819550
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer11/09/2018
Date Manufacturer Received11/09/2018
Was Device Evaluated by Manufacturer? No
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
-
-