FDA Device recall Z-0863-2022
Lum Lam Custom Pack - Anesthesia Kit
- FDA Device
- Class II
- ongoing
- Published 2022-04-13
On 2022-04-13 the FDA classified a Class II recall of Lum Lam Custom Pack - Anesthesia Kit by Stradis Medical, citing the outer bag may be perforated or torn, which may result in a breach in the sterility of the kit.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0863-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-02-25 |
| Published | 2022-04-13 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Stradis Medical |
| Distribution | US |
Product
Lum Lam Custom Pack - Anesthesia Kit
Reason
The outer bag may be perforated or torn, which may result in a breach in the sterility of the kit.
Identifiers
| code_info | SKU/Part Number 570-2674; UDI H65257026741 Lot Numbers: 21300478831 and 21314479685 |
|---|
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-0863-2022%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.