BD Pet Syringes, 0.5mL x 12MM, U-100 323003Recalls & reported problems
Becton, Dickinson and Company Inc · SYRINGE 0.5ML 29GA 12MM U100 VET 10BAG 500CS · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382903230020), received between Jun 20, 2018 and Oct 14, 2019 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Defective Device” (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
- Defective Device1
- Delivered as Unsterile Product1
- Device Contamination with Chemical or Other Material1
- Suction Problem1
Patient problems
- No Known Impact Or Consequence To Patient3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 14, 2019Delivered as Unsterile Product; Defective Device; Delivered as Unsterile Product; Defective Device
IT WAS REPORTED THAT BD PET SYRINGE HAD A BROKEN THUMB PRESS AND A CRUSHED CAP. THIS WAS DISCOVERED DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 323003 BATCH NO: 6294537. IT WAS REPORTED BY THE CONSUMER THAT ONE SYRINGE WAS FOUND WITH A BROKEN THUMB PRESS AND A CRUSHED CAP. ISSUE(S): FOUND 1 SYRINGE WITH PLUNGER ROD THUMB PRESS BROKEN AND SAME SYRINGE PLUNGER CAP CRUSHED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9187432 ↗MalfunctionSep 25, 2019Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT FOREIGN MATTER WAS DISCOVERED WITH A BD SYRINGE 0.5ML 29G 12.7MM. THIS OCCURRED ON 2 SEPARATE OCCASIONS DURING USE, HOWEVER, THE DATE/TIME INFORMATION IS UNKNOWN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED THAT BLACK FOREIGN MATTER WAS FOUND WITHIN THE SYRINGE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9119313 ↗MalfunctionJun 20, 2018Suction Problem
IT WAS BROUGHT TO MY ATTENTION, ON A NUMBER OF OCCASIONS, WHEN AN INSULIN SYRINGE WAS INSERTED INTO THE INSULIN, IT FAILED TO DRAW THE INSULIN FROM THE VIAL, JUST AIR.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7619144 ↗
Other Syringe, piston devices
- BD Luer-Lok 309657Becton, Dickinson And Company · Syringe, piston1,266 reports
- 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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