MAUDE Adverse Event Report: BECTON DICKINSON BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET; TUBES, VIALS, SYSTEMS, SERUM SEPARATORS, BLOOD COLLECTION

Catalog Number	367283
Medical Device Problem Codes	Product Quality Problem (1506); Physical Resistance/Sticking (4012)
Health Effect - Clinical Code	Needle Stick/Puncture (2462)
Date of Event	06/02/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
E1: initial reporter facility name: (b)(6).The manufacturing location for this product is nipro.This site is an oem manufacturing site.Therefore, bd corporate headquarters in franklin lakes, nj has been listed in sections d.3.And g.1.And the franklin lakes fda registration number has been used for the manufacture report number.B3: date of event is unknown.The date received by manufacturer has been used for this field.D4.Medical device expiration date: unknown.H4.Device manufacture date: unknown.D4.Medical device lot#: unknown.A device evaluation and/or device history review is anticipated but is not complete.Upon completion, a supplemental report will be filed.
Event or Problem Description
It was reported that while using four bd vacutainer® safety-lok¿ blood collection set, the customer obtained needle stick injury due to unfamiliarity with the device.There was no health impact or consequence reported.
Additional Manufacturer Narrative
The following fields have been updated with corrected and/or additional information.Date received by manufacturer: 02-july-20245 b1: adverse event b2: other-dirty needlestick injury b5: describe event: it was reported that while using four bd vacutainer® safety-lok¿ blood collection set, the customer obtained needle stick injury due to unfamiliarity with the device.There was no health impact or consequence reported.Reported verbatim: due to unfamiliarity with slbcs operation, needle pricking occurred.
Event or Problem Description
It was reported that while using four bd vacutainer® safety-lok¿ blood collection set, the customer obtained needle stick injury due to unfamiliarity with the device.There was no health impact or consequence reported.Reported verbatim: due to unfamiliarity with slbcs operation, needle pricking occurred.
Additional Manufacturer Narrative
Investigation summary: bd had not received samples or photos for evaluation.Additionally, bd was unable to determine the specific lot number associated with this complaint; therefore, a review of the device history record could not be conducted.However, the shipping inspection record of 466 lots from the product concerned (#367283) manufactured in from april 2024 to march 2025 was investigated and no abnormalities were found.This complaint is unable to be confirmed.If additional information is made available, this complaint will be reopened to assess the level of investigation needed.Complaints received for this device and reported condition will continue to be tracked and trended.Our business team regularly reviews the collected data for identification of emerging trends.
Event or Problem Description
It was reported that while using four bd vacutainer® safety-lok¿ blood collection set, the customer obtained needle stick injury due to unfamiliarity with the device.There was no health impact or consequence reported.Reported verbatim: due to unfamiliarity with slbcs operation, needle pricking occurred.

• Brand Name: BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET
• Common Device Name: TUBES, VIALS, SYSTEMS, SERUM SEPARATORS, BLOOD COLLECTION
• Manufacturer (Section D): BECTON DICKINSON; 1 becton drive; franklin lakes NJ 07417
• Manufacturer (Section G): BECTON DICKINSON; 1 becton drive; franklin lakes NJ 07417
• Manufacturer Contact: matt j. connor ; 7 loveton circle; sparks, MD 21152 ; 4103164000
• MDR Report Key: 22370062
• Report Number: 2243072-2025-00813
• Device Sequence Number: 4437545
• Product Code: JKA
• UDI-Device Identifier: 30382903672838
• UDI-Public: (01)30382903672838
• Combination Product (Y/N): N
• Initial Reporter Country: TW
• PMA/510(K) Number: K980414
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 07/14/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Catalogue Number: 367283
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/02/2025
• Supplement Date Received by Manufacturer: 07/02/2025; 07/14/2025
• Initial Report FDA Received Date: 07/01/2025
• Supplement Report FDA Received Date: 07/02/2025; 08/12/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown