MAUDE Adverse Event Report: BD MEDICAL (BD WEST) MEDICAL SURGICAL SYRINGE 3ML SALINE 3ML FILL; SALINE, VASCULAR ACCESS FLUSH

Catalog Number 306544

Device Problem Device Contamination with Chemical or Other Material (2944)

Patient Problem No Consequences Or Impact To Patient (2199)

Event Date 12/14/2020

Event Type  malfunction  

Manufacturer Narrative

The customer's address is unknown:  (b)(6) usa has been used as a default.  investigation summary: a device history record review was completed by our quality engineer team for provided lot number 203206.The review did not reveal any detected abnormalities during the production process that could have contributed to this defect and all quality tests were found to be within specification.One physical sample was received by our quality team for evaluation.The sample came in a plastic bag and had no packaging flow wrap.A visual inspection was performed and the tip cap and luer tip show a discoloration.An attempt to remove it with an alcohol wipe was done with no success.An ftir could not be performed.The cause for this defect could have resulted during the tip cap molding process where the tip cap got contaminated with lubricant from the molding press and when the tip cap was assembled to the barrel then barrel got similar discoloration on the luer tip.As a result of this incident, the tip cap molding press was inspected finding it clean with no residues of lubricant or any other material.Further action has not been determined necessary at this time.Our quality team will continue to monitor the manufacturing process for this defect and other emerging trends.Investigation conclusion: based on the investigation and with no sample analysis the symptom reported by the customer could not be confirmed.We will continue monitoring the complaint trend for this product and symptom.Probable root cause: tip cap molding process.It could be possible that the tip cap got contaminated with lubricant from the molding press.When the tip cap was assembled to the barrel then barrel got similar discoloration on the luer tip.The tip cap molding press was inspected finding it clean with no residues of lubricant or any other material.(b)(4).

Event Description

It was reported that the syringe 3ml saline 3ml fill experienced foreign matter contamination.The following information was provided by the initial reporter: material no: 306544 batch no: 0203206.Product name and/or catalog number: bd posiflush (3ml ns flush).Lot number or serial number: 0203206.Any injuries and/or harm? none known.What is the issue you experienced? pink substance on syringe hub.

• Brand Name: SYRINGE 3ML SALINE 3ML FILL
• Type of Device: SALINE, VASCULAR ACCESS FLUSH
• Manufacturer (Section D): BD MEDICAL (BD WEST) MEDICAL SURGICAL; 1852 10th avenue; columbus NE 68601
• Manufacturer (Section G): BD MEDICAL (BD WEST) MEDICAL SURGICAL; 1852 10th avenue; columbus NE 68601
• Manufacturer Contact: brett wilko ; 9450 south state street; sandy, UT 84070 ; 8015296192
• MDR Report Key: 11163573
• MDR Text Key: 227577005
• Report Number: 1911916-2021-00025
• Device Sequence Number: 1
• Product Code: NGT
• UDI-Device Identifier: 00382903065448
• UDI-Public: 00382903065448
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K161552
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: other,user facility
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 01/07/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/13/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Other
• Device Expiration Date: 06/30/2023
• Device Catalogue Number: 306544
• Device Lot Number: 0203206
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 12/21/2021
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 12/15/2020
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 07/21/2020
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1