GE Healthcare Clinical Systems GE LOGIQ 3 Expert ultrasound scanner with software versions 4.0.5, 4.1.1 and 4.1.2. GE Healthcare P.O. Box 414, Milwaukee, Wisconsin 53201 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
GE LOGIQ 3 Expert ultrasound scanner with software versions 4.0.5, 4.1.1 and 4.1.2. GE Healthcare P.O. Box 414, Milwaukee, Wisconsin 53201
Brand
GE Healthcare Clinical Systems
Lot Codes / Batch Numbers
Systems with software version 4.0.5, 4.1.1 and 4.1.2. Serial numbers: 26022WS4, 26023WS2, 26346WS7, 2641WS8, 31001WS1, 34381WS4, 36460WS4, 36461WS2, 43734WS3, 43735WS0, 43736WS8, 43737WS6, 43994WS3, 43995WS0, 43998WS4, 44000WS8, 44001WS6, 44002WS4, 44003WS2, 44004WS0, 44005WS7, 44011WS5, 44012WS3, 44013WS1, 44015WS6, 44016WS4, 44018WS0, 44019WS8, 44020WS6, 44100WS6, 44153WS5, 44157WS6, 44159WS2, 44270WS7, 44273WS1, 44274WS9, 44275WS6, 44276WS4, 44277WS2, 44532WS0, 44533WS8, 44817WS5, 44819WS1, 44820WS9, 44821WS7, 44822WS5, 44825WS8, 44826WS6, 44908WS2, 44909WS0, 44912WS4, 44914WS0, 44915WS7, 44989WS2, 44990WS0, 44991WS8, 44992WS6, 44994WS2, 45088WS2, 45089WS0, 5122WS7
Products Sold
Systems with software version 4.0.5, 4.1.1 and 4.1.2. Serial numbers: 26022WS4, 26023WS2, 26346WS7, 2641WS8, 31001WS1, 34381WS4, 36460WS4, 36461WS2, 43734WS3, 43735WS0, 43736WS8, 43737WS6, 43994WS3, 43995WS0, 43998WS4, 44000WS8, 44001WS6, 44002WS4, 44003WS2, 44004WS0, 44005WS7, 44011WS5, 44012WS3, 44013WS1, 44015WS6, 44016WS4, 44018WS0, 44019WS8, 44020WS6, 44100WS6, 44153WS5, 44157WS6, 44159WS2, 44270WS7, 44273WS1, 44274WS9, 44275WS6, 44276WS4, 44277WS2, 44532WS0, 44533WS8, 44817WS5, 44819WS1, 44820WS9, 44821WS7, 44822WS5, 44825WS8, 44826WS6, 44908WS2, 44909WS0, 44912WS4, 44914WS0, 44915WS7, 44989WS2, 44990WS0, 44991WS8, 44992WS6, 44994WS2, 45088WS2, 45089WS0, 5122WS7
GE Healthcare Clinical Systems is recalling GE LOGIQ 3 Expert ultrasound scanner with software versions 4.0.5, 4.1.1 and 4.1.2. GE Healthcare due to Inaccurate guidelines: The BE9C is an optional, small radius Bi-planar convex probe intended for use with the LOGIQ 3 Expert system in Urology applica. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Inaccurate guidelines: The BE9C is an optional, small radius Bi-planar convex probe intended for use with the LOGIQ 3 Expert system in Urology application. An attempt by the user to activate the biopsy guidelines while this probe is in use will cause incorrect guidelines to be displayed on the image. The incorrect guidelines are recognized by their orientation that is left/right reversed from t
Recommended Action
Per FDA guidance
GE sent consignees a "GE Urgent Medical Device Correction" letter dated 8/14/07. The letter informed the customers about the problem, offer a short-term workaround and informed them that a representative will schedule a visit to upgrade the software.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, NY
Page updated: Jan 10, 2026