KING LTS-D KitRecalls & reported problems across all models
King Systems Corporation · 4 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
4 open recalls name at least one KING LTS-D Kit model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 4
We found 4 models of KING LTS-D Kit by King Systems Corporation in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
4 FDA recall records name at least one of these models by its device identifier, 4 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
KING LTS-D Kit recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Sep 26, 2024Open, Classified
Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.
Z-0276-2025 · Root cause: No Marketing Application · Recall details · FDA record ↗
- Sep 26, 2024Open, Classified
Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.
Z-0275-2025 · Root cause: No Marketing Application · Recall details · FDA record ↗
- Sep 26, 2024Open, Classified
Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.
Z-0274-2025 · Root cause: No Marketing Application · Recall details · FDA record ↗
- Sep 26, 2024Open, Classified
Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.
Z-0273-2025 · Root cause: No Marketing Application · Recall details · FDA record ↗
KING LTS-D Kit models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- KING LTS-D Kit KLTSD430AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- KING LTS-D Kit KLTSD431AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- KING LTS-D Kit KLTSD432AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- KING LTS-D Kit KLTSD4325AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
Other King Systems Corporation products
All King Systems Corporation devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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