BD Ultra-Fine Insulin Syringes, 1/2mL 30G x 1/2 - Kaiser 329407Recalls & reported problems
Becton, Dickinson and Company Inc · SYRINGE 0.5ML 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 00382903294077), received between Jan 3, 2020 and Dec 7, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- 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.
MalfunctionDec 7, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT 2 BD 0.5ML SYRINGES EXPERIENCED HUB SEPARATION FROM THE DEVICE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER REPORTED FINDING 2 SYRINGES NEEDLE SHIELDS AND HUBS LAYING IN THE BAG.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12954401 ↗MalfunctionJan 3, 2020Leak/Splash; Leak/Splash
IT WAS REPORTED THAT TWO SYRINGE 0.5ML 30GA X 1/2IN EXPERIENCED HUB SEPARATION FROM THE DEVICE DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 329407; BATCH NO. 7016828, UNKNOWN. VERBATIM: ISSUE: CONSUMER REPORTED WHEN HE REMOVES THE NEEDLE SHIELD NEEDLE STAYS INSIDE THE NEEDLE SHIELD. INCIDENT DATE- (B)(6) 2019; OCCURENCE-1; ITEM# 329407; LOT# 7016828. ISSUE: CONSUMER REPORTED WHEN HE PULLED THE SHIELD, OFF, NEEDLE REMAINED INSIDE THE NEEDLE SHIELD. INCIDENT DATE-UNKNOWN; OCCURENCE-1; ITEM# 329407; LOT# UNKNOWN. CONSUMER USES THE NEW NEEDLE EACH TIME OF HIS INJECTION. OFFERED TO SEND THE REPLACEMENT TO THE DISTRIBUTOR.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9547136 ↗
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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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