FDA Medical Device Recalls (openFDA)
Philips Medical Systems: Gyroscan ACS-NT system
- Recall number
- Z-1199-03
- Recalling firm
- Philips Medical Systems
- Product
- Gyroscan ACS-NT system
- Status
- Terminated
- Initiated
- 2002-05-02
- Posted
- 2003-09-12
- Terminated
- 2005-04-11
- Reason
- Patient burns related to high SAR levels and the combined use of Synergy Body Coil and synergy Flex-M coil
- Root cause
- Other
- Action
- The firm issued a Field Change Order to their field personnel instructing them to add new labeling to the User Manual. 05/02/2002 A letter was issued to customers.
- Quantity
- 112 total for all 3 devices
- Distribution
- The firm distributed units to hospitals and medical centers nationwide.
- Lot, serial or model codes
- X1753, X1412, X1595, X1662, 102718, X1757, X1693, X1523, X1740, X1742, 86293, 101206, 86292, X0717, X1602, X1563, X1670, X1648, X1582, 10009, 10353, 86280, 13057, 13056, 4139, 87605, 84700, 86968, 10082, 87604, 86082, 101111, 84899, 87183, 87161, 87146, 86020, 87135, 86121, 86080, 101608, X0083, 87148, 87145, 83306, 83303, 86184, 86147, 84478, 87188, X1759, 86559, 85685, 102095, 83804, 100460, 85433, 83802, 82678, 85119, 83946, 84433, 86019, 83301, 84861, 84860, 87527, 84820, 100786, 84477, 100785, 86083, 101072, 100459, 83325, 84887, 86056, 87147, 83396, 86596, 85684, 62832, 85500, 85688, 86406, 86411, 100916, 85422, 100469, 85686, 86407, 87310, 87309, 86595, 85139, 85172, 63046, 101408, 85141, 86335, 86317, 87033, 85157, 101165, 38317, 86334, 47189,86287, 86288, 101429, 87053
- 510(k) numbers
- K932645
- PMA numbers
- not on file
- Product code
- LNH
- Firm FEI
- 1000524572
- Firm city
- Bothell
- Firm state
- WA
- 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