Brand Name: recall status ⚠ Recalls found. Brand Name is named in 4 official recalls in our current data:
FDA Class II recall Z-2710-2026 — Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.FDA Class II recall Z-2711-2026 — Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.FDA Class II recall Z-2712-2026 — Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.And 1 more listed below. Source checks: October 22, 2026 at 6:00 PM UTC (oldest successful check).
Sources, dates and coverage limits We collect recent notices on a six-hour schedule using a rolling 90-day source request. Older retained records may also appear. This is a recall index, not a catalogue of all products or a complete recall history.
CPSC: stored recall dates April 30, 2026 to October 22, 2026. NHTSA: stored recall dates April 24, 2026 to October 19, 2026. FDA: stored recall dates April 29, 2026 to October 14, 2026. USDA FSIS is not aggregated here. Check USDA meat, poultry and processed egg notices . EPA and U.S. Coast Guard are not aggregated. Source delays and missing identifiers can prevent a match.
Brand Elekta Recalls naming this model FDA Class II · Medical device · July 15, 2026
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
Company / brand: Elekta recalls
Affected product: Brand Name recall status
Official ID Z-2710-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
Company / brand: Elekta recalls
Affected product: Brand Name recall status
Official ID Z-2711-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
Company / brand: Elekta recalls
Affected product: Brand Name recall status
Official ID Z-2712-2026 ·
Official record ↗
FDA Class II · Medical device · May 6, 2026
Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.
Company / brand: Elekta recalls
Affected product: Brand Name recall status
Official ID Z-2006-2026 ·
Official record ↗
See all Elekta recalls →
Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.