OptiChamber Diamond 00 (REF 1097502)Recalls & reported problems
Respironics Respiratory Drug Delivery (Uk) Ltd · OptiChamber Diamond Anti-Static Valved Holding Chamber · Class 2
- 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 00383730000145), received between Jan 5, 2021 and Jan 5, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device Problem” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 5, 2021Use of Device Problem
A REPORTER CALLED TO REPORT AN ADVERSE EVENT AS A RESULT OF USING A WRONG DEVICE WHICH WAS GIVEN TO THEM BY A (B)(6) PHARMACIST. HER GRANDSON WAS PRESCRIBED FOR A NEBULIZER FOR HIS BRONCHITIS. HOWEVER, THE PHARMACIST GAVE THEM A SPACER FOR INHALER. SHE SAID THE PHARMACIST DID THIS INTENTIONALLY BECAUSE WHEN HE WAS ASKED THAT WAS NOT HER GRANDSON'S PRESCRIPTION, HE CLAIMED IT SHOULD WORK THE SAME WAY. THE REPORTER SAID AS A RESULT HER GRANDSON'S CONDITION WORSEN SINCE HE DID NOT GET HIS MEDICATION AS HE SHOULD. THE REPORTER SAID SINCE SHE IS A REGISTERED NURSE, SHE FIGURED OUT THAT IT WAS A WRONG DEVICE AND CORRECTED THE PROBLEM.
Patient problems: Insufficient Information
MAUDE report 11125318 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.