BD BBL™ Bio-Bag™ Environmental Chamber Type C 261212Recalls & reported problems
Becton, Dickinson And Company · Bag Bio-Bag Type Cfj 25 Ea · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30382902612125), received between Jul 11, 2018 and Jul 11, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- Laceration(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 11, 2018Break
IT WAS REPORTED THAT WHILE USING A BD BBL¿ BIO-BAG¿ ENVIRONMENTAL CHAMBER TYPE CFJ A LAB ASSISTANT WAS CUT THROUGH THEIR GLOVE ATTEMPTING TO CRUSH THE GLASS AMPOULE. THE LAB ASSISTANT RECEIVED MEDICAL INTERVENTION AT AN EMERGENCY ROOM FOLLOWING THE INCIDENT.
Patient problems: Laceration(s)
MAUDE report 7679811 ↗
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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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