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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: C.R. BARD, INC. (COVINGTON) -1018233 BARD 60CC PISTON IRRIGATION SYRINGE

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C.R. BARD, INC. (COVINGTON) -1018233 BARD 60CC PISTON IRRIGATION SYRINGE Back to Search Results
Model Number 750375
Device Problem Manufacturing, Packaging or Shipping Problem (2975)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  malfunction  
Manufacturer Narrative
The investigation is still in progress.Once the investigation is complete, a supplemental report will be filed.The device was not returned.
 
Event Description
It was reported that the syringes were empty and did not contain the saline water as normal.
 
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Brand Name
BARD 60CC PISTON IRRIGATION SYRINGE
Type of Device
SYRINGE
Manufacturer (Section D)
C.R. BARD, INC. (COVINGTON) -1018233
8195 industrial blvd
covington GA 30014
Manufacturer (Section G)
C.R. BARD, INC. (COVINGTON) -1018233
8195 industrial blvd
covington GA 30014
Manufacturer Contact
yonic anderson
8195 industrial blvd
covington, GA 30014
7707846100
MDR Report Key9608115
MDR Text Key180395514
Report Number1018233-2020-00442
Device Sequence Number1
Product Code KYZ
UDI-Device Identifier00801741051142
UDI-Public(01)00801741051142
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
EXEMPT
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Other,Consumer,Distributor
Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date 01/20/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received01/20/2020
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model Number750375
Device Catalogue Number750375
Was Device Available for Evaluation? No
Date Manufacturer Received12/30/2019
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
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