INJEKT™ 4606728V-02Recalls & reported problems
B. Braun Medical Inc. · Injekt™ 10 mL LL Syringe · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046964002953), received between Aug 25, 2025 and Aug 25, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination /Decontamination 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.
Reports received per month
Most reported problems
Device problems
- Contamination /Decontamination Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 25, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem
AS REPORTED BY THE USER FACILITY: HI MY NAME IS (B)(6) I'M CALLING FROM THE (B)(6) PHARMACY IN (B)(6). I WAS JUST CALLING TO REPORT A PRODUCT COMPLAINT REGARDING 1 THE SYRINGES THAT THE B. BRAUN PRODUCES IT IS THE INJECT SYRINGE WITH THE LUER LOCK, THE LOT NUMBER IS 23B20C8, WE RECENTLY DISCOVERED THAT IN THE BARREL OF THE SYRINGE THERE'S SOME PLASTIC RESIDUE AND FLAKES THAT CAME OFF, WE WERE JUST CONCERNED IF IT WASN'T CAUGHT THEN IT COULD HAVE BEEN INJECTED INTO A PATIENT AND SO WE JUST TO ATTENTION IN CASE THIS WAS A PROBLEM WITH OTHER THIS LOT, SO IF YOU COULD JUST BE WITH THE CALL BACK (B)(6), THAT WOULD BE GREAT, YOU CAN ALSO REACH US BY EMAIL IT IS (B)(6) THANK YOU BYE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22884612 ↗
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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
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- 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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