King Systems recalls

King Systems has 26 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 6 Nov 2024. 8 are still ongoing. The most frequent reason is sterility.

Total recalls26since 2012
Last 12 months0reported
Class I28% of total
Ongoing8latest 6 Nov 2024

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 2 8%Class II 23 88%Class III 1 4%

Why king systems is recalled

By year

Ongoing king systems recalls

8 active

All king systems recalls, newest first

26 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIKing Ltsd,Size 2,W/Suction Port Sterile-Inserted into recalledKing SystemsOtherNationwide
DeviceCLASS IIKing Ltsd,Size 2.5, W/Suction Port Sterile-Inserted into recalledKing SystemsOtherNationwide
DeviceCLASS IIKing Ltsd,Size 0, W/Suction Port Non-sterile Kit-Inserted recalledKing SystemsOtherNationwide
DeviceCLASS IIKing Ltsd,Size 2, W/Suction Port Non-sterile Kit-Inserted recalledKing SystemsOtherNationwide
DeviceCLASS IIKing Ltsd,Size 1, W/Suction Port Non-sterile Kit-Inserted recalledKing SystemsOtherNationwide
DeviceCLASS IIKing Ltsd,Size 2.5, W/Suction Port Non-sterile Kit-Inserted recalledKing SystemsOtherNationwide
DeviceCLASS IIKing Ltsd,Size 1,W/Suction Port Sterile-Inserted into recalledKing SystemsOtherNationwide
DeviceCLASS IIAmbu / King Ltsd, Size 0,1 W/Suction Port recalled by King SystemsKing SystemsOtherNationwide
DeviceCLASS IKing Vision Video Adapter Size 1/2 recalled by King SystemsKing SystemsOtherNationwide
DeviceCLASS IIKing Lts-d Kit Size recalled by King SystemsKing SystemsPackaging Defects11 states
DeviceCLASS IIUniversal Flex2 Breathing Circuit recalled by King SystemsKing SystemsPackaging Defects43 states
DeviceCLASS IIDouble Swivel Connector with Suction Port Connector, Airway recalledKing SystemsLabeling ErrorsNationwide
DeviceCLASS IIKLTSD414 Quantity King Ltsd Kit Size 4 King LT(S)-Dtm recalledKing SystemsPackaging DefectsCA, NY
DeviceCLASS IUniversal Flex2 Breathing Circuit Class I 510(k) Exempt recalledKing SystemsOtherNationwide
DeviceCLASS IIKing Lts-d Oropharyngeal Airways recalled by King SystemsKing SystemsPackaging DefectsNationwide
DeviceCLASS IIIKing Lt-d Oropharyngeal Airways The King Lt-d is intended recalledKing SystemsPackaging DefectsNY
DeviceCLASS IIKing Lad Standard ClearSeal Single Use recalled by King SystemsKing SystemsSterilityNationwide
DeviceCLASS IIKing Lad Sili Cone Single Use, King Systems recalledKing SystemsSterilityNationwide
DeviceCLASS IIKing Lad Standard ClearSeal Single Use recalled by King SystemsKing SystemsSterilityNationwide
DeviceCLASS IIKing Lad Sili Cone Single Use, King Systems recalledKing SystemsSterilityNationwide
DeviceCLASS IIKing Lad Sili Cone Single Use, King Systems devices/case recalledKing SystemsSterilityNationwide
DeviceCLASS IIKing Lad Standard ClearSeal Single Use recalled by King SystemsKing SystemsSterilityNationwide
DeviceCLASS IIKing Lad Standard ClearSeal Single Use recalled by King SystemsKing SystemsSterilityNationwide
DeviceCLASS IIKing Lad Sili Cone Single Use, King Systems recalledKing SystemsSterilityNationwide
DeviceCLASS IIKing Lad Flexible ClearSeal Single Use recalled by King SystemsKing SystemsSterilityNationwide
DeviceCLASS IIKing Lad Flexible ClearSeal Single Use recalled by King SystemsKing SystemsSterilityNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.