FDA released a warning letter regarding device failures involving Beta Bionics, Inc.
4 reports, 3 independent
Updated Oct 23
Gone quiet
- Reports
- 4
- Developments
- 2
- Repetition
- 50%
New informationRepeats or wire copies
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What happened
FDA released a warning letter regarding device failures involving Beta Bionics, Inc.
Who's involved
What this event is mainly aboutHow it developed
Newest first. Tap a step to see who reported it.FDA issued Form 483 and warning letters concerning Beta Bionics' iLet Bionic Pancreas.1 source
FDA issued a warning letter to Beta Bionics, Inc. over device failures.1 source
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The entities involved
- FDA
-
BETA BIONICS, INC.
Nothing else this week.
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