King LTS-D Kit Size 1 — Class II medical device recall Z-1681-2019
Terminated recall by King Systems Corp. dba Ambu, Inc., reported 2019-06-05, distributed in CA, CT, FL, IA, IN, MD, MS, NC…. Size 0 products were incorrectly packaged and labeled as a size 1 products.
| Recall number | Z-1681-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | King Systems Corp. dba Ambu, Inc., Noblesville, IN, United States |
| Recall initiated | 2019-01-04 |
| Classified | 2019-05-29 |
| Reported by FDA | 2019-06-05 |
| Terminated | 2020-04-20 |
| Distributed | CA, CT, FL, IA, IN, MD, MS, NC, PA, TX, WI |
| Quantity | 270 |
| Reason classes | labeling |
| Lot numbers | 1000147351 |
| Model numbers | KLTSD431 |
Product
King LTS-D Kit Size 1, Model Number KLTSD431
Reason for recall
Size 0 products were incorrectly packaged and labeled as a size 1 products.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1681-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.