FDA Medical Device Recalls (openFDA)
Hamilton Medical, Inc.: Hamilton-MR1, REF: 161010, Intensive Care Ventilator
- Recall number
- Z-2528-2023
- Recalling firm
- Hamilton Medical, Inc.
- Product
- Hamilton-MR1, REF: 161010, Intensive Care Ventilator
- Status
- Open, Classified
- Initiated
- 2023-07-26
- Posted
- 2023-09-20
- Terminated
- not on file
- Reason
- Degrading capacitors on the control board of ventilators and spare parts may leak electrolyte onto the control board causing a short circuit on the board and/or the capacitor to lose function and lead to interruption of ventilation.
- Root cause
- Nonconforming Material/Component
- Action
- On July 26, 2023, Hamilton Medical issued Urgent Medical Device Correction via E-Mail. Hamilton Medical asked consignees to take the following actions 1. Check for affected devices in your facility. Get in contact with your local distribution partner and get the devices serviced with high priority. 2. Please sign the enclosed/attached sheet to confirm that, as an End- Customer, you have received and duly noted this Medical Device Correction.
- Quantity
- 12 units
- Distribution
- Distribution US nationwide, including Puerto Rico. OUS: Not provided
- Lot, serial or model codes
- UDI: 07630002800761 & 07630002813556 / Affected Serial Numbers: 3422 3423 3424 3425 3426 3427 3428 3429 3469 3503 3510 3800
- 510(k) numbers
- ["K153046"]
- PMA numbers
- not on file
- Product code
- CBK
- Firm FEI
- 2937708
- Firm city
- Reno
- Firm state
- NV
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28