FDA Device recall Z-1779-2019
Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use…
- FDA Device
- Class II
- terminated
- Published 2019-06-19
On 2019-06-19 the FDA classified a Class II recall of Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use… by Skytron Div The Kmw Group, citing weld attaching the air heater assembly to the main sterilizer unit has shown signs of fatigue/failure.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1779-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-18 |
| Published | 2019-06-19 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Skytron Div The Kmw Group |
| Distribution | US |
Product
Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use in health care facilities. The Integrity Sterilizer incorporates high-pressure steam to sterilize nonporous or porous items and materials used in the health care industry
Reason
Weld attaching the air heater assembly to the main sterilizer unit has shown signs of fatigue/failure
Identifiers
| code_info | Serial Numbers: 14092619, 14092620, 14102621, 17123520, 18113521 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1779-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.