FDA Device recall Z-1211-2022
Drager SafeStar 55, Catalog No. MP01790
- FDA Device
- Class I
- ongoing
- Published 2022-06-22
On 2022-06-22 the FDA classified a Class I recall of Drager SafeStar 55, Catalog No. MP01790 by Draeger Medical, citing possible occlusion of filters due to manufacturing error.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1211-2022 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2022-05-16 |
| Published | 2022-06-22 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Draeger Medical |
| Distribution | US |
Product
Drager SafeStar 55, Catalog No. MP01790
Reason
Possible occlusion of filters due to manufacturing error.
Identifiers
| code_info | UDI-DI: 04048675026785; Lot No. LT2103. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1211-2022%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.