FDA Device recall Z-1939-2020
SWIN 2017 database, Model YSW4000
- FDA Device
- Class II
- terminated
- Published 2020-05-20
On 2020-05-20 the FDA classified a Class II recall of SWIN 2017 database, Model YSW4000 by Remel, citing potential for out of range microbial results.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1939-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-01-04 |
| Published | 2020-05-20 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Remel |
| Distribution | n/a |
Product
SWIN 2017 database, Model YSW4000
Reason
Potential for out of range microbial results
Identifiers
| code_info | ... |
|---|
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-1939-2020%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.