FDA Medical Device Recalls (openFDA)
Ge Healthcare, Llc: GE Healthcare, Innova 2100IQ (The Digital Fluoroscopic Imaging System consists of an a monoplane positioner, a vascular or cardiac table, an X-ray system and a digital detector)
- Recall number
- Z-1661-2010
- Recalling firm
- Ge Healthcare, Llc
- Product
- GE Healthcare, Innova 2100IQ (The Digital Fluoroscopic Imaging System consists of an a monoplane positioner, a vascular or cardiac table, an X-ray system and a digital detector)
- Status
- Terminated
- Initiated
- 2010-03-24
- Posted
- 2010-05-26
- Terminated
- 2013-05-21
- Reason
- A potential software failure related to the Worklist functionality has been identified on a subset of Innova 2100IQ, 3100IQ and 4100IQ systems. When using the Worklist function to import patient data to Innova, there are two scenarios that will cause the next exam to fail and the inability to recall acquired sequences.
- Root cause
- Software design
- Action
- Consignees were sent on 3/24/10, a GE Healthcare " Urgent Medical Device Correction" letter dated March 23, 2010. The letter included the Safety Issue, Affected Product Details, Product Correction and Contact Information.
- Quantity
- 92
- Distribution
- Worldwide distribution: USA, Puerto Rico, VENEZUELA, UNITED KINGDOM, TURKEY, THAILAND, TAIWAN, PROVINCE OF CHINA, SWEDEN, SPAIN, RUSSIAN FEDERATION, ROMANIA, POLAND, PHILIPPINES, NORWAY, NETHERLANDS, MOROCCO, REPUBLIC OF KOREA, KAZAKSTAN, JAPAN, ITALY, ISLAMIC REPUBLIC OF IRAN, INDONESIA, INDIA, GERMANY, FRANCE, FINLAND, EGYPT, CHINA, CHILE, CANADA, BRAZIL, BELGIUM, BELARUS, AUSTRALIA, and ARGENTINA.
- Lot, serial or model codes
- 0000009C2M0012 0000008C2M0005 0000009C2M0019 0000009C2M0017 0000009C2M0008 0000009C2M0015 0000009C2M0027 0000008C2M0002 0000009C2M0020 0000009C2M0048 0000009C2M0038 0000009C2M0050 0000009C2M0022 0000009C2M0051 0000009C2M0052 0000009C2M0011 0000009C2M0045 0000009C2M0086 0000009C2M0034 0000009C2M0073 0000009C2M0080 0000009C2M0066 0000009C2M0087 0000009C2M0070 0000009C2M0055 0000009C2M0061 0000009C2M0047 0000009C2M0091 0000009C2M0075 0000009C2M0031 0000009C2M0102 0000009C2M0094 0000009C2M0095 0000009C2M0103 0000009C2M0121 0000009C2M0069 0000009C2M0141 0000009C2M0135 0000009C2M0123 0000009C2M0159 0000009C2M0098 0000009C2M0146 0000009C2M0018 0000009C2M0153 0000009C2M0168 0000009C2M0145 0000009C2M0107 0000009C2M0142 0000009C2M0203 0000009C2M0114 0000009C2M0129 0000009C2M0170 0000009C2M0169 0000009C2M0182 0000009C2M0044 0000009C2M0125 0000009C2M0190 0000009C2M0201 0000009C2M0152 0000009C2M0140 0000009C2M0184 0000010C2M0001 0000009C2M0039 0000009C2M0035 0000009C2M0036 0000009C2M0043 0000009C2M0132 0000009C2M0151 0000009C2M0164 0000009C2M0172 0000009C2M0196 0000009C2M0207 0000009C2M0183 0000009C2M0206 0000009C2M0113 0000009C2M0105 0000009C2M0191 0000009C2M0174 0000009C2M0137 0000009C2M0133 0000009C2M0134 0000009C2M0138 0000009C2M0161 0000009C2M0181 0000009C2M0198 0000010C2M0016 0000009C2M0089 0000009C2M0204 0000009C2M0079 0000009C2M0186 0000009C2M0165 0000009C2M0076
- 510(k) numbers
- ["K050489","K052157","K052412","K061163"]
- PMA numbers
- not on file
- Product code
- MQB
- Firm FEI
- 2126677
- Firm city
- Waukesha
- Firm state
- WI
- 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