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All product recalls associated with GE Medical Systems, LLC.
Total Recalls
1000
Past Year
421
Class I (Serious)
53
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Breathing circuit inner tube may separate from the rigid connectors under certain conditions. A separation of the inner tube from the connector may prevent adequate gas flow (O2, N2O and anesthetic agents) to the patient. A separation can also cause CO2 re-breathing. This could lead to hypoxia and/or hypercarbia and inadequate anesthesia delivery.
The recalled candles were sold under the DayNa Decker "Botanika" brand in 16-ounce green glass vessels, 4 inches wide by 5 inches high. Botanika candles in the smaller 3-ounce and 6-ounce sizes are not included in the recall. The words "DayNa Decker" and "Bacara," "Bardou," "Clementine," "Indigo," "Leila," "Manzanita," "Sierra," "Violetta," "Yasmin" or "Zelia" appear on the bottom of the glass vessel.
Signa MR Excite" 1.5T system containing 11.1_M4_0818.a software, associated with 2D Fast Spin Echo based pulse sequences (2D FSE-XL, 2D FRFSE-XL, 2D FSE-IR, 2D T2FLAIR and 2D T1FLAIR) may experience an image flip along the phase encode direction and incorrect annotation, which may result in incorrect localization of anatomy in oblique axial images with the pulse sequences.