FDA Device recall Z-1681-2019
King LTS-D Kit Size 1, Model Number KLTSD431
- FDA Device
- Class II
- terminated
- Published 2019-06-05
On 2019-06-05 the FDA classified a Class II recall of King LTS-D Kit Size 1, Model Number KLTSD431 by King Systems, citing size 0 products were incorrectly packaged and labeled as a size 1 products.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1681-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-01-04 |
| Published | 2019-06-05 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | King Systems |
| Distribution | CA, CT, FL, IA, IN, MD, MS, NC, PA, TX, WI |
Product
King LTS-D Kit Size 1, Model Number KLTSD431
Reason
Size 0 products were incorrectly packaged and labeled as a size 1 products.
Identifiers
| code_info | Lot code 1000147351 |
|---|
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-1681-2019%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.