King Systems Corp. dba Ambu, Inc. recalls

8 recalls on record · latest: September 26, 2024

Official U.S. recall history for King Systems Corp. dba Ambu, Inc., compiled from official government records.

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King Systems Corp. dba Ambu, Inc. recalls KING LTSD,SIZE 2,W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the mouth to provide patent airway. M…

September 26, 2024 · Medical device recalls Moderate risk Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it i…

King Systems Corp. dba Ambu, Inc. recalls KING LTSD,SIZE 2.5, W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the mouth to provide patent airway…

September 26, 2024 · Medical device recalls Moderate risk Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it i…

KING LTSD recalled over sterility concerns

September 26, 2024 · Medical device recalls Moderate risk Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it i…

KING LTSD recalled over sterility concerns

September 26, 2024 · Medical device recalls Moderate risk Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it i…

KING LTSD recalled over sterility concerns

September 26, 2024 · Medical device recalls Moderate risk Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it i…

KING LTSD recalled over sterility concerns

September 26, 2024 · Medical device recalls Moderate risk Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it i…

King Systems Corp. dba Ambu, Inc. recalls KING LTSD,SIZE 1,W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the mouth to provide patent airway. M…

September 26, 2024 · Medical device recalls Moderate risk Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it i…

King Systems Corp. dba Ambu, Inc. recalls AMBU / KING LTSD, SIZE 0,1 W/SUCTION PORT, STERILE- Inserted into a patient s pharynx through the mouth to provide pate…

September 26, 2024 · Medical device recalls Moderate risk Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it i…