King Systems Corp. dba Ambu, Inc.: Medical Device Recall in 2019 - (Recall #: Z-1681-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

King LTS-D Kit Size 1, Model Number KLTSD431

Product Classification:

Class II

Date Initiated: January 4, 2019

Date Posted: June 5, 2019

Recall Number: Z-1681-2019

Event ID: 82036

Reason for Recall:

Size 0 products were incorrectly packaged and labeled as a size 1 products.

Status: Terminated

Product Quantity: 270

Code Information:

Lot code 1000147351

Distribution Pattern:

The products were distributed to the following US states: CA, CT, FL, IA, IN, MD, MS, NC, PA, TX, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated