B.BRAUN S9902-10Recalls & reported problems
B. Braun Medical Inc. · Evacuated IV Container, Glass, 250 mL · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04046964187797), received between Nov 17, 2021 and Nov 17, 2021 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Improper Flow or Infusion” (2 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Improper Flow or Infusion2
Patient problems
- Air Embolism2
- Hypoxia2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 17, 2021Improper Flow or Infusion; Improper Flow or Infusion
AS REPORTED BY THE USER FACILITY: AIR FILLED THE IV TUBING TOWARD THE PATIENT INSTEAD OF PULLING OUT BLOOD INTO THE BOTTLE. AIR IN TUBING DID NOT REACH THE PATIENT. IT WAS IMMEDIATELY CLAMPED. THE PATIENT WAS NOT HARMED.
Patient problems: Air Embolism; Hypoxia; No Clinical Signs, Symptoms or Conditions
MAUDE report 12826787 ↗InjuryNov 17, 2021Improper Flow or Infusion; Improper Flow or Infusion
AS REPORTED BY THE USER FACILITY: AIR FILLED THE IV TUBING TOWARD THE PATIENT INSTEAD OF PULLING OUT BLOOD INTO THE BOTTLE. THE PATIENT WENT TO THE ED VIA AMBULANCE FOR HYPOXIA. PATIENT RECEIVED OXYGEN TREATMENT AND FULLY RECOVERED.
Patient problems: Air Embolism; Hypoxia
MAUDE report 12826785 ↗
Other CONTAINER, I.V. devices
- INTRAVIA 2B8011Baxter International Inc. · CONTAINER, I.V.127 reports
- INTRAVIA 2B8012Baxter International Inc. · CONTAINER, I.V.119 reports
- APEX™ 2112531B. Braun Medical Inc. · CONTAINER, I.V.69 reports
- APEX™ 2112530B. Braun Medical Inc. · CONTAINER, I.V.66 reports
- INTRAVIA 2B8013Baxter International Inc. · CONTAINER, I.V.64 reports
- SECURE® 66040Metrix Company, The · Container, I.V.1 recall8 reports
- MICROTEK 1Microtek Medical LLC · CONTAINER, I.V.1 recall8 reports
- SECURE® 66045Metrix Company, The · Container, I.V.1 recall7 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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