CLASSIC HYPERBARIC
Received Aug 23, 2022 · Event occurred Aug 12, 2022
Report MW5111688 · MDR key 15283211
Device
Generic name
Chamber, Hyperbaric
Manufacturer
UnkProduct problems
- Adverse Event Without Identified Device or Use Problem
Patient
Unknown
- Convulsion/Seizure
- Convulsion/Seizure
Narrative
Description of Event or Problem
SEIZURE IN CLASSIC HYPERBARIC CHAMBER. FDA SAFETY REPORT ID# (B)(4).