FDA Medical Device Recalls (openFDA)
Pelton & Crane Company: Pelton & Crane Dental Chairs, Spirit 1500 with magnetic headrest, Pelton & Crane, Charlotte, NC 28273. Intended for the properly positioning of patients to perform dental procedures.
- Recall number
- Z-1180-2010
- Recalling firm
- Pelton & Crane Company
- Product
- Pelton & Crane Dental Chairs, Spirit 1500 with magnetic headrest, Pelton & Crane, Charlotte, NC 28273. Intended for the properly positioning of patients to perform dental procedures.
- Status
- Terminated
- Initiated
- 2010-02-24
- Posted
- 2010-04-01
- Terminated
- 2010-10-28
- Reason
- Magnetic headrests may affect patients with implantable pacemakers and defibrillators.
- Root cause
- Device Design
- Action
- Pelton & Crane Issued an "Urgent Field Safety Alert" notification dated February 24, 2010. Consignees were instructed of the affected product and informed of proper actions to take. For further information, contact Pelton & Crane at 1-704-588-2126.
- Quantity
- Total: 498 chairs and 619 replacement upholstery spare parts
- Distribution
- Worldwide Distribution -- United States, Australia, the Netherlands, Canada and Germany.
- Lot, serial or model codes
- All Devices with Model Number SP15
- 510(k) numbers
- ["K760404"]
- PMA numbers
- not on file
- Product code
- KLC
- Firm FEI
- 1017522
- Firm city
- Charlotte
- Firm state
- NC
- 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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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