Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of GetingeLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Getinge USA Sales with 48 device recalls. The most recent is a device recall dated Jan 15, 2025: Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 15, 2025 | Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For usClass I · Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health c | Device recalls |
| Oct 3, 2024 | MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical inClass II · Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. Thi | Device recalls |
| Oct 3, 2024 | MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical inClass II · Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. Thi | Device recalls |
| Oct 3, 2024 | MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical inClass II · Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. Thi | Device recalls |
| Oct 3, 2024 | MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical inClass II · Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. Thi | Device recalls |
| Oct 3, 2024 | MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical inClass II · Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. Thi | Device recalls |
| Oct 3, 2024 | MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical inClass II · Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. Thi | Device recalls |
| Oct 3, 2024 | MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical inClass II · Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. Thi | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
