MAUDE Adverse Event Report: CARDINAL HEALTH MONOJCT NDL 27X1-1/2; NEEDLE, HYPODERMIC, SINGLE LUMEN

Model Number	1188827112
Medical Device Problem Code	Incomplete or Inadequate Connection (4037)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Event or Problem Description
The customer reported that the 27-gauge needles are supposed to lock onto the syringes and they don¿t lock.They keep spinning when they put them onto the syringe.Per additional information received on 18mar2022, there wasn¿t any harm done.They used a different needle they had purchased previously and there were no problems.
Additional Manufacturer Narrative
An investigation is currently underway.Upon completion, the results will be forwarded.
Additional Manufacturer Narrative
The device history record was reviewed and indicated that the product was released accomplishing all quality standards.Prior to a lot¿s release, the lot must be deemed acceptable by passing inspections that are based on a valid sampling plan.Inspectors routinely examine a statistical sample both physically and visually.Specifically, the parts are inspected for damaged components and leakage in fluid pathway.The reported lot met all defined acceptance requirements and was released.396 unused sample were received for evaluation.The samples were visually inspected and functionally tested however the reported condition could not be confirmed therefore there is insufficient information to determine the root cause.Furthermore there were no anomalies found during a review of the dhrs, maintenance records or process monitoring data and there was no evidence of any systemic failure of the manufacturing process.Based on the investigation and root cause analysis, the initiation of a corrective and preventative action is not required at this time.This complaint will be used for tracking and trending purposes.

• Brand Name: MONOJCT NDL 27X1-1/2
• Common Device Name: NEEDLE, HYPODERMIC, SINGLE LUMEN
• Manufacturer (Section D): CARDINAL HEALTH; 2010 east international speedw; deland FL 32724
• Manufacturer (Section G): CARDINAL HEALTH; 2010 east international speedw; deland FL 32724
• Manufacturer Contact: jill saraiva ; 777 west street; mansfield, MA 02048 ; 5086183640
• MDR Report Key: 13998842
• Report Number: 1017768-2022-01008
• Device Sequence Number: 4895425
• Product Code: FMI
• UDI-Device Identifier: 10884521007444
• UDI-Public: 10884521007444
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 07/25/2022

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 Model Number: 1188827112
• Device Catalogue Number: 1188827112
• Device Lot Number: 135434
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 03/15/2022
• Supplement Date Received by Manufacturer: 03/15/2022
• Initial Report FDA Received Date: 04/04/2022
• Supplement Report FDA Received Date: 07/25/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 12/10/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: A
• Patient Sequence Number: 1
• Patient Sex: Unknown