Class II — King Systems Corp. dba Ambu, Inc.
| Recalling firm | KING SYSTEMS |
|---|---|
| Registered facility | KING SYSTEMS CORPORATION. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Size 0 products were incorrectly packaged and labeled as a size 1 products. |
| Product | King LTS-D Kit Size 1, Model Number KLTSD431 |
| Quantity | 270 |
| Distribution | The products were distributed to the following US states: CA, CT, FL, IA, IN, MD, MS, NC, PA, TX, and WI. |
| Initiated | 2019-01-04 |
| Classified | 2019-05-29 |
| Terminated | 2020-04-20 |
| Recall number | Z-1681-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — King Systems Corp. dba Ambu, Inc. (Z-1681-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82036/
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