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 GE HealthCareLabelled 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 Vital Signs Devices with 3 device recalls. The most recent is a device recall dated Jul 18, 2013: Disposable Temperature Probes, (sterile), Sensor diameter: 3mm/0.12 in; 25 units per box….
| Jul 18, 2013 | Disposable Temperature Probes, (sterile), Sensor diameter: 3mm/0.12 in; 25 units per box. Vital Signs Inc. a GE Healthcare Company, 20 CampuClass II · GE Healthcare has become aware of a potential safety issue associated with the use of GE General Purpose 9 French Temper | Device recalls |
| Oct 16, 2012 | Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal scalp circular (spiral) electrode and applicator is a device useClass II · Thirty fetal scalp electrodes were found to have an incomplete package seal and lacked the printed lot number stamped on | Device recalls |
| Feb 20, 2012 | enFlow IV Fluid Warmer (510k name: EFLOW IV FLUID WARMER, MODEL 100, EFLOW DISPOSABLE CARTRIDGE, MODEL 200 AND EFLOW AC POWER SUPPLY, MODEClass II · The EnFlow Warmer Strap does not meet the requirements of the biocompatibility standard (ISO 10993) for products that m | 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
