FreshRecalls

Elekta recalls

5 recent recalls on record for Elekta in CPSC, NHTSA, and FDA data as of July 24, 2026 at 12:00 AM UTC.

Models with recalls

Brand Name (4)MOSAIQ Oncology Information System (1)

All Elekta recalls

FDA Class II · Medical device · July 15, 2026

Brand Name recall — Elekta, Inc.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

Official ID Z-2712-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Brand Name recall — Elekta, Inc.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

Official ID Z-2711-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Brand Name recall — Elekta, Inc.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

Official ID Z-2710-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

MOSAIQ Oncology Information System recall — Elekta, Inc.

Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.

Official ID Z-2406-2026 · Official record ↗

FDA Class II · Medical device · May 6, 2026

Brand Name recall — Elekta, Inc.

Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.

Official ID Z-2006-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked July 24, 2026 at 12:00 AM UTC.