MAUDE Adverse Event Report: ZYNO MEDICAL LLC ZYNO MEDICAL ADMINISTRATION SET FOR Z-800 INFUSION PUMP; IV ADMINISTRATION SET

Model Number	B2-70072-F
Medical Device Problem Code	Device Operates Differently Than Expected (2913)
Health Effect - Clinical Code	Not Applicable (3189)
Date of Event	01/24/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
One zyno customer service employee followed up with the user over the phone.The user reported that when he primed any of the carefusion primary set, it leaked at the luer lock.The zyno employee explained that sometimes during priming, fluid can be stored in the luer lock if the luer lock cover is on.The zyno employee advised the user that the luer lock cover could be taken off before priming the set in the future.Alternatively, the user can leave the cover on, and when he primes the carefusion set, he should pay attention to the luer lock and stop priming when he sees that the set is fully primed.The user also reported that when he closed the roller clamp on the secondary set, it doesn't stop the fluid and caused a leak.The zyno employee asked the user to send any fields set that are available back to zyno to initiate the evaluation, but was informed that no sets were saved.The user was advised to contact zyno's territory manager if future issue arise and save the samples for evaluation.
Event or Problem Description
The user reported that they were "having an issue with the tubing sets leaking even though they are clamped" and "they are leaking before getting to the pumps".He also reported that "this is happening with all three sets that we use" and he has "closed all clamps on the primary lines and it still leaks".No patients were involved and various medications were used.

• Brand Name: ZYNO MEDICAL ADMINISTRATION SET FOR Z-800 INFUSION PUMP
• Common Device Name: IV ADMINISTRATION SET
• Manufacturer (Section D): ZYNO MEDICAL LLC; 177 pine street; natick MA 01760
• MDR Report Key: 6331301
• Report Number: 3006575795-2017-00041
• Device Sequence Number: 11189975
• Product Code: FPA
• UDI-Device Identifier: 00814371020204
• UDI-Public: 00814371020204
• Combination Product (Y/N): N
• Initial Reporter State: AL
• Initial Reporter Country: US
• PMA/510(K) Number: K132841
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Nurse
• Type of Report: Initial
• Report Date (Section B): 02/10/2017

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
• Operator of Device: Health Professional
• Device Model Number: B2-70072-F
• Device Lot Number: 16088363
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/24/2017
• Initial Report FDA Received Date: 02/15/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1