MAUDE Adverse Event Report: CARDINAL HEALTH 12ML LUER LOCK TIP PHARM TRAY; SYRINGE, PISTON

Model Number 8881512258

Device Problem Device Contaminated During Manufacture or Shipping (2969)

Patient Problem Insufficient Information (4580)

Event Type  malfunction  

Manufacturer Narrative

The incident sample has been requested but to date has not been received for evaluation.  if the sample is received, or if additional information pertinent to the incident is obtained a follow-up report will be submitted.  as part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product.

Event Description

Customer reports: when filling the syringes, there are black particles found in some of the syringes and white particles in other syringes from the lot.The customer sent the product to a 3rd party lab for analysis and the white fibers were identified as cellulose with silicone and oxygen-rich surface particles and the black fiber defects were identified as textile cotton fibers with spectral indications of silicone.

Manufacturer Narrative

One sample of a monoject syringe with 12ml liquid without the original package or lot number identification was received for evaluation.The component is produced by external supplier and the assembly process consists of a pick and place operation at the cardinal health facility.The root cause for the condition was requested from the manufacturer and will be documented through the supplier notification and response form.There is no additional inspection on the line to detect the reported condition.We are awaiting an action plan to be implement by the supplier for the corrective actions.The cardinal health facility will continue monitoring the process for any adverse trends that require immediate attention.

• Brand Name: 12ML LUER LOCK TIP PHARM TRAY
• Type of Device: SYRINGE, PISTON
• Manufacturer (Section D): CARDINAL HEALTH; calle 9 sur no. 125 cuidad ind; tijuana 22500 ; MX 22500
• MDR Report Key: 12170198
• MDR Text Key: 263460992
• Report Number: 9612030-2021-02983
• Device Sequence Number: 1
• Product Code: FMF
• UDI-Device Identifier: 10884521010970
• UDI-Public: 10884521010970
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,distri
• Type of Report: Initial,Followup
• Report Date: 09/08/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/14/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Device Model Number: 8881512258
• Device Catalogue Number: 8881512258
• Device Lot Number: 1925340064
• Date Manufacturer Received: 07/06/2021
• Patient Sequence Number: 1