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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CURAD SIZE D COMPRESSION STOCKINGS; STOCKING, MEDICAL SUPPORT
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CURAD SIZE D COMPRESSION STOCKINGS; STOCKING, MEDICAL SUPPORT Back to Search Results
Device Problems Improper or Incorrect Procedure or Method (2017); Data Problem (3196)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  No Answer Provided  
Event Description
The facility received an order for curad 20-30mmhg size d compression stockings.However, the order should have been for a size a compression stocking.Investigation results: after a review of the above issues, the following was determined.Type of medication error: incorrect product; was the medication administered to the resident? na.Area where error occurred: data entry and initial review medication (s) / product(s) involved: curad size d compression stocking vs curad size a compression stockings, order error potential: low root cause: the measurements on the prescription was clearly written.In accordance with policy and procedure, the data entry technician should have entered the correct size according to the measurements on the order.In accordance with policy and procedure, the pharmacist should have verified the correct size according to the measurements and deviated from established policy and procedure by approving the order as correct.The data entry technician and pharmacist were not in present time with the prescription.(b)(6); access number: (b)(4).
 
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Brand Name
CURAD SIZE D COMPRESSION STOCKINGS
Type of Device
STOCKING, MEDICAL SUPPORT
MDR Report Key8228498
MDR Text Key132792394
Report NumberMW5082944
Device Sequence Number1
Product Code FQL
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 05/23/2018
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
Device Operator No Information
Initial Date Manufacturer Received Not provided
Initial Date FDA Received01/07/2019
Type of Device Usage N
Patient Sequence Number1
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