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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HEPARIN LOCK FLUSH 1ML SYRINGE; SALINE, VASCULAR ACCESS FLUSH

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HEPARIN LOCK FLUSH 1ML SYRINGE; SALINE, VASCULAR ACCESS FLUSH Back to Search Results
Patient Problem Insufficient Information (4580)
Event Type  Other  
Event Description
Pharmacy received an email from our nursing manager that the wrong heparin flushes were stocked in our automated dispensing cabinet.Normally, the unit keeps heparin flush 10 units/ml 5 ml syringes (50 units/5ml) stocked.The unit ran out and asked the pharmacy to stock more during the day.The technician accidentally stocked heparin flush 10 units/ml 1 ml syringes.The products look nearly identical so it's easy to see how they were mixed up.Unsure how the barcode was bypassed when stocking the adc.Ref report: mw5150459.(b)(4).
 
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Brand Name
HEPARIN LOCK FLUSH 1ML SYRINGE
Type of Device
SALINE, VASCULAR ACCESS FLUSH
MDR Report Key18534976
MDR Text Key333259669
Report NumberMW5150460
Device Sequence Number1
Product Code NGT
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Unknown
Type of Report Initial
Report Date 01/17/2024
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? No
Initial Date Manufacturer Received Not provided
Initial Date FDA Received01/17/2024
Patient Sequence Number1
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