InjuryCBF
CLASSIC HYPERBARIC
Received May 16, 2022 · Event occurred Apr 12, 2022
Report MW5109752 · MDR key 14416900
Device
Generic name
Chamber, Hyperbaric
Manufacturer
UnkProduct problems
- Unexpected Therapeutic Results
Patient
Unknown
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
Narrative
Description of Event or Problem
USED A FAULTY CHAMBER AT A CLINIC. (B)(6). FDA SAFETY REPORT ID# (B)(4).