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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ZEVEX, INC. ZEVEX FEEDING PUMP; PUMP, INFUSION, ENTERAL

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ZEVEX, INC. ZEVEX FEEDING PUMP; PUMP, INFUSION, ENTERAL Back to Search Results
Patient Problem Insufficient Information (4580)
Event Date 02/15/2024
Event Type  malfunction  
Event Description
(b)(6), (b)(6) medical equipment and supplies to individual pts and facilities.I want to make a complaint about the cleanliness of the equipment being sent out to pts.(b)(6) was cleaning the zevex feeding pumps and joey feeding pumps, (b)(6) removed the cleaning products from the work station and (b)(6) to use "soap and warm water" to clean the equipment.However, as i'm sure you know, soap and water is not a disinfectant and does not kill disease carrying bacteria.Secondly, there is currently a part of medical equipment sitting outside of ( ) warehouse.Out in the open.I asked (b)(6) "why is this cart with equipment sitting outside of the building?" and was told "it has bugs in it".Well, equipment that has bugs in it is supposed to be put into a bug-zapper tent and ran for at least 8-12 hours.Leaving a ventilator with bugs in it outside in the cold does not kill the bugs.Bed bugs can live up to 6 months.This is not sanitary and not okay to be giving out dirty/but infested equipment to pts.(b)(6) spoken (b)(6) supervisors, managers, and even (b)(6) cco (b)(6).But these things keep happening.(b)(6).It's unfair to (b)(6) pts.Please help.(b)(6), (b)(6).
 
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Brand Name
ZEVEX FEEDING PUMP
Type of Device
PUMP, INFUSION, ENTERAL
Manufacturer (Section D)
ZEVEX, INC.
MDR Report Key19115792
MDR Text Key340424632
Report NumberMW5153869
Device Sequence Number1
Product Code LZH
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 03/04/2024
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
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received04/15/2024
Patient Sequence Number1
Patient Outcome(s) Other;
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