BD Ultra-Fine Insulin Syringes, 1ml 30G x 1/2 - Kaiser 329406Recalls & reported problems
Becton, Dickinson and Company Inc · SYRINGE 1.0ML 30GA No Ins · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00382903294060), received between Jul 10, 2019 and Feb 26, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Device Markings/Labelling Problem1
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 26, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT THE EXPIRATION DATE WAS MISSING ON SHELF PACK WITH A BD ULTRA-FINE¿ INSULIN SYRINGES, 1ML 30G X 1/2 . THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED THAT EXPIRATION DATE WAS NOT ON SHELF CARTON. CONSUMER WANTED TO KNOW IF SYRINGES WERE STILL GOOD TO USE. STATED, DID NOT SEE EXPIRATION DATE.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient
MAUDE report 11387846 ↗MalfunctionJul 10, 2019Leak/Splash; Leak/Splash
IT WAS REPORTED THAT IT WAS DIFFICULT TO MOVE THE BD ULTRA-FINE II¿ INSULIN SYRINGE PLUNGER WHILE DELIVERING INSULIN. THIS WAS DISCOVERED DURING USE. NO DATE/TIME OR PATIENT INFORMATION WAS GIVEN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 329406, BATCH NO. UNKNOWN. IT WAS REPORTED THAT IT IS DIFFICULT TO DEPRESS THE PLUNGER WHILE DELIVERING INSULIN. COMMENTS: I HAVE BEEN USING YOUR PRODUCT NO. 329406 FOR LAST FIVE YEARS. LATELY IT HAS BEEN VERY DIFFICULT TO PRESS THE PLUNGER WHILE DELIVERING THE INSULIN. I WAS ABLE TO DO IT WITH ONE HAND. NOW IT TAKES BOTH HANDS AND THAT ALSO WITH SOME DIFFICULTY. SOMETHING IS CHANGED. EITHER THE INSIDE DIA. IS TOO TIGHT OR THE THICKNESS OF THE PLUNGER IS ON HIGH SIDE. IT LOOKS A TOLERANCE PROBLEM. PL. CHECK. THE BAR CODE ON ONE OF THE BAGS IS (B)(4).
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8776134 ↗
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- BD Luer-Lok 309653Becton, Dickinson And Company · Syringe, piston948 reports
- BD Luer-Lok 309628Becton, Dickinson And Company · Syringe, piston862 reports
- N/A 302995Becton, Dickinson And Company · Syringe, piston1 recall537 reports
- BD Plastipak Syringe 300865Becton, Dickinson And Company · Syringe, piston515 reports
- N/A 302830Becton, Dickinson And Company · Syringe, piston462 reports
- N/A 302832Becton, Dickinson And Company · Syringe, piston424 reports
- BD Ultra-Fine 328468Becton, Dickinson and Company Inc · Syringe, piston323 reports
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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