BD Oral Syringe 305220Recalls & reported problems
Becton, Dickinson And Company · SYRINGE ORAL 3ML CLEAR · Class 1
All models of BD Oral Syringe (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 30382903052203), received between Jan 5, 2024 and Jan 22, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (3 reports).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Device Markings/Labelling Problem3
- Defective Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 22, 2026Device Markings/Labelling Problem
IT WAS REPORTED THAT BD SYRINGE ORAL 3ML CLEAR LABEL CONTENT WAS INCORRECT. RCC RECEIVED A COMPLAINT VIA EMAIL. CALLER STATES ONE OF HIS CUSTOMERS CALLED STATING THAT THEY ORDERED 3ML CLEAR ORAL SYRINGE 305220. THE LABEL ON THE PACKAGING STATES 1ML CLEAR ORAL SYRINGE BUT THERE IS A 3ML CLEAR ORAL SYRINGE INSIDE OF THE PACKAGING. CUSTOMER WANTED TO KNOW IF THERE ARE ANY RECALLS ON THIS PRODUCT AND IS IT SAFE TO USE. LOT#: 5010407.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24149050 ↗MalfunctionApr 11, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT THE BD ORAL SYRINGE LABEL CONTENT WAS INCORRECT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED BY CUSTOMER THAT THEY RECEIVED PRODUCT WITH WRONG LABEL HAVING DIFFERENT MATERIAL NUMBER. VERBATIM: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. PRODUCT COMPLAINT - CUSTOMER CALLED TO REPORT THAT THEY RECEIVED MISLABEL PRODUCT, THE OUTER CASES IS LISTED AS (B)(6) LOT 3195317, WHILE (B)(4) BAGS OF A 100EA IS LABEL (B)(6), THE PHYSICAL PRODUCT APPEARS TO BE THE OUTER CARTON LABEL. DOE (B)(6) 2024, SAMPLE AVAILABLE, NOT USED. NO PT HARM, CUSTOMER REQUESTS REPLACEMENT (B)(4) OF PRODUCT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19091076 ↗MalfunctionJan 29, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18594860 ↗MalfunctionJan 5, 2024Defective Component; Defective Component
IT WAS REPORTED THAT BD SYRINGE ORAL 3ML CLEAR STOPPER WAS DEFECTIVE / DAMAGED IT WAS REPORTED BY CUSTOMER THAT THEY HAVE HAD TO DISPOSE OF SEVERAL OF OUR SYRINGES ALREADY FROM ONE BAG BECAUSE THE RUBBER PART INSIDE IS CROOKED AND MAKES HIS DOSAGE INACCURATE. VERBATIM: RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. HELLO, MY SON IS A TRANSPLANT RECIPIENT AND RELIES ON ACCURATE MEDICATION DOSAGES. I HAVE HAD TO DISPOSE OF SEVERAL OF YOUR SYRINGES ALREADY FROM ONE BAG BECAUSE THE RUBBER PART INSIDE IS CROOKED AND MAKES HIS DOSAGE INACCURATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18455008 ↗
Other CONTAINER, LIQUID MEDICATION, GRADUATED devices
- BD Luer Tip Caps 308341Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED1 recall3 reports
- BD Oral Syringe 305210Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED11 reports
- 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 305218Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED3 reports
- BD Luer-Lok Female Cap 408531Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED3 reports
- BD Syringe Tip Cap 305819Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED3 reports
- BD Oral Syringe 305219Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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