FDA Device recall Z-1460-2023
Anesthesia Circuit Kit Coax HEPA, MP17102
- FDA Device
- Class I
- terminated
- Published 2023-05-24
On 2023-05-24 the FDA classified a Class I recall of Anesthesia Circuit Kit Coax HEPA, MP17102 by Draeger Medical, citing glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1460-2023 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2023-04-17 |
| Published | 2023-05-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Draeger Medical |
| Distribution | US |
Product
Anesthesia Circuit Kit Coax HEPA, MP17102
Reason
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Identifiers
| code_info | UDI-DI: 04048675695622; All lots. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Other recalls by Draeger Medical
- Brand Name: Atlan Product Name: Atlan A300 Model/Catalog Number: 8211300 The Atlan is an anesthesia workstation intended for use in anesthe…
FDA Device · Class I · 2024-12-25 · Draeger Medical - Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstation intended for use in anest…
FDA Device · Class I · 2024-12-25 · Draeger Medical - Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component: Not applicable
FDA Device · Class I · 2024-11-20 · Draeger Medical - Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable
FDA Device · Class I · 2024-11-20 · Draeger Medical - Dr¿ger Perseus A500 Anesthesia Workstation
FDA Device · Class I · 2024-04-24 · Draeger Medical
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1460-2023%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.