Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator: recall status
⚠ Recalls found. Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator is named in 3 official recalls in our current data:
FDA Class II recall Z-1939-2026 — The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
FDA Class II recall Z-1940-2026 — The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
FDA Class II recall Z-1941-2026 — The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.