BD Syringe Tip Cap 305819Recalls & reported problems
Becton, Dickinson And Company · CAP TIP SYR LL/LS STER LF PP BLUE SINGLE · Class 1
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382903058198), received between Oct 27, 2022 and Mar 20, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Device Contamination with Chemical or Other Material1
- Expiration Date Error1
- Volume Accuracy Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 20, 2026Volume Accuracy Problem; Device Contamination with Chemical or Other Material
THE CUSTOMER OBSERVED LIQUID PRESENT INSIDE THE TIP CAP. ADDITIONAL INFORMATION THERE WAS NO PATIENT HARM AS THIS WAS CAUGHT BY A PHARMACIST AND SUBSEQUENTLY THE TIP CAP WAS CHANGED TO AN ALTERNATIVE TIP CAP BEFORE DISPENSING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24649429 ↗MalfunctionOct 27, 2023Expiration Date Error; Expiration Date Error
MATERIAL#: 305819; BATCH: 3227156. IT WAS REPORTED BY CUSTOMER THAT THE CUSTOMER REPORTS THEY WERE MADE AWARE ON 10/20/23, OF EXPIRATION DATE ON THE LABEL. THE LABEL DOES NOT MATCH CERTIFICATE SHOWS A 2 MONTH DIFFERENCE, QUANTITY OF 5 CASES HAVE BEEN IMPACTED, 2000 PER CASES. DISTRIBUTOR: THERMO FISHER. THE CUSTOMER ALSO REQUESTS A REPLACEMENT. VERBATIM: NO ADDITIONAL INFORMATION RECEIVED. RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. THE CUSTOMER REPORTS THEY WERE MADE AWARE ON 10/20/23, OF EXPIRATION DATE ON THE LABEL. THE LABEL DOES NOT MATCH CERTIFICATE SHOWS A 2 MONTH DIFFERENCE, QUANTITY OF 5 CASES HAVE BEEN IMPACTED, 2000 PER CASES. DISTRIBUTOR: THERMO FISHER. THE CUSTOMER ALSO REQUESTS A REPLACEMENT. REF# (B)(4). LOT# 3227156.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18022378 ↗InjuryOct 27, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE CONSUMER ALLEGEDLY DEVELOPED HEPATITIS C AND AIDS AFTER USING THE BD¿ SYRINGE TIP CAP BULK STERILE CONVENIENCE PACK. NO FURTHER INFORMATION WAS PROVIDED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "I AM... A VICTIM OF HEP C THAT YOUR INFECTED NEEDLES AND AIDS THAT I GOT FROM USING YOUR INFECTED: NO COBALT IRRADIATED NOT STERILE PRODUCT."
Patient problems: Insufficient Information
MAUDE report 15678834 ↗
Other CONTAINER, LIQUID MEDICATION, GRADUATED devices
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- BD Oral Syringe 305209Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED6 reports
- BD Oral Syringe 305207Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED5 reports
- BD Oral Syringe 305220Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED4 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.