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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. BD INSYTE AUTOGUARD BC; PERIPHERAL IV CATHETERS

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BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. BD INSYTE AUTOGUARD BC; PERIPHERAL IV CATHETERS Back to Search Results
Catalog Number 382634
Device Problem Retraction Problem (1536)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 03/04/2024
Event Type  malfunction  
Manufacturer Narrative
Address information was not provided, therefore, xx was used as a place holder.If a device evaluation and/or device history review is completed, a supplemental report will be filed.
 
Event Description
It was reported that an unspecified amount of bd insyte autoguard bcs encountered resistance while retracting the needle.The following information was provided by the initial reporter: end user is having resistance when pulling back the needle which is causing blood to leak out the back end and looks like the valve is being broken to remove the needle.Additional information received 03/08/2024: date of events unknown no sample available did the event directly, or indirectly involve a patient or user? yes several occurrences.
 
Manufacturer Narrative
Additional information: additional event details from customer added to b5.Investigation results: the reported defect could not be refuted nor confirmed in the absence of a sample.The root cause cannot be determined for an unconfirmed defect.The dhr for lot 3342665 has been reviewed.Subassembly lot 3342665 material 7000bcw34 was built on afa line 9 from 10dec023 through 14dec2023.Final lot was packaged on pkg line 10 from 17dec2023 through 18dec2023 for a total quantity of (b)(4).No related quality issues or process deviations were found.This complaint type will continue to be trended within the post market surveillance process and any determined escalation will be managed there.
 
Event Description
Additional information: no problems with the needle retraction spring.Once the colored part is off the hub, the needle comes in contact with colored hub creating resistance when threading.There has been no visible damage seen.Blood exposures to any surfaces have not been reported, other than the bed, floor and patient.No reports of serious injuries or harm.No medical or surgical interventions were needed for any events.Reported from multiple rns, many different patients, and lot numbers were not noted.It seems it is mainly the non-blood control needles.The main problem seen is resistance when threading due to needle touching the plastic colored part of the cannula once it is unseated.
 
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Brand Name
BD INSYTE AUTOGUARD BC
Type of Device
PERIPHERAL IV CATHETERS
Manufacturer (Section D)
BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.
9450 south state street
sandy UT 84070
Manufacturer (Section G)
BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.
9450 south state street
sandy UT 84070
Manufacturer Contact
helen cox (mdr)
75 north fairway drive
vernon hills, IL 60061
8473935694
MDR Report Key18934829
MDR Text Key338661669
Report Number1710034-2024-00200
Device Sequence Number1
Product Code FOZ
UDI-Device Identifier00382903826346
UDI-Public(01)00382903826346
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K201075
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type User Facility
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 03/27/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Catalogue Number382634
Device Lot Number3342665
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received 03/04/2024
Initial Date FDA Received03/19/2024
Supplement Dates Manufacturer Received03/27/2024
Supplement Dates FDA Received04/18/2024
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured12/19/2023
Is the Device Single Use? Yes
Type of Device Usage Initial
Patient Sequence Number1
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