MAUDE Adverse Event Report: BECTON DICKINSON MEDICAL SYSTEMS BD SYRINGE 10ML LL TIP BULK CONVENIENCE PAK; PISTON SRYINGE

Catalog Number	309605
Medical Device Problem Codes	Break (1069); Defective Component (2292)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/09/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the bd syringe 10ml ll tip bulk convenience pak plunger rod was broken / damaged.The following information was provided by the initial reporter: material #:309605 batch#: unknown (potential lot provided 4297537, 4354977) it was reported by a customer that the defective plunger, foreign particulate, syringe markings and deformed syringe fluid in cap.Verbatim: rcc received a complaint via email.During visual inspection of lot #20250909-1e80e2 the following were found, all units are available for return.Two lot #s was used and it is unknown which belongs to the complaints.Syringe plunger - 3 foreign particulate - 1 syringe markings - 1 deformed syringe fluid in cap- 3 (b)(6) 2025 (b)(4) sterile syringe tray 10ml 302995 expiry 9/30/209 and 11-30-2029 lot # 4297537, 4354977 syringe plunger = 3 (b)(6) 2025 (b)(4) sterile syringe tray 10ml 302995 expiry 9/30/209 and 11-30-2029 4297537, 4354977 foreign particulate = 1 (b)(6) 2025 (b)(4) sterile syringe tray 10ml 302995 expiry 9/30/209 and 11-30-2029 4297537, 4354977 syringe markings = 1 (b)(6) 2025 (b)(4) sterile syringe tray 10ml 302995 expiry 9/30/209 and 11-30-2029 4297537, 4354977 all units are available for return.Two lot #s was used and it is unknown which belongs to the complaints.
Additional Manufacturer Narrative
H.3.If a device evaluation and/or device history review is completed, a supplemental report will be filed.
Additional Manufacturer Narrative
(b)(4) - supplemental mdr - plunger rod broken / damaged eight samples of 10 ml ll syringes (part number 309605) were evaluated, revealing two main issues: one bag contained a syringe with approximately 50% of the scale markings missing, and another bag with three syringes had visibly distorted stoppers.A third bag appeared defect-free, though an unused sample from the same batch is recommended for further review.One sample from a fourth bag was excluded due to contamination.Fourier transform infrared spectroscopy (ftir) analysis confirmed silicone material but could not determine whether the quantity was normal or excessive due to contamination.The missing print defect is likely related to the marking process, while the distorted stopper defect is associated with the assembly process.Furthermore, a device history record review was completed for the provided lot numbers 4297537 and 4354977.The review showed no rejected inspections or quality issues during production that could have contributed to the reported defects.Complaints received for this device and reported condition will continue to be tracked and trended.Information will be captured in trend reports and monitored monthly.Our business team regularly reviews the collected data to identify emerging trends.
Event or Problem Description
No additional information was provided.

• Brand Name: BD SYRINGE 10ML LL TIP BULK CONVENIENCE PAK
• Common Device Name: PISTON SRYINGE
• Manufacturer (Section D): BECTON DICKINSON MEDICAL SYSTEMS; route 7 and grace way; canaan CT 06018
• Manufacturer (Section G): BECTON DICKINSON MEDICAL SYSTEMS; route 7 and grace way; canaan CT 06018
• Manufacturer Contact: helen cox (mdr) ; 75 north fairway drive; vernon hills, IL 60061 ; 8473935694
• MDR Report Key: 23354277
• Report Number: 1213809-2025-00668
• Device Sequence Number: 8824036
• Product Code: FMF
• UDI-Device Identifier: 30382903096054
• UDI-Public: (01)30382903096054(17)290930(10)4297537
• Combination Product (Y/N): N
• Initial Reporter State: MO
• Initial Reporter Country: US
• PMA/510(K) Number: K110771
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 12/23/2025

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 Catalogue Number: 309605
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 10/13/2025
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/02/2025
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 10/21/2025
• Supplement Report FDA Received Date: 12/22/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown