King Systems Corp.: Medical Device Recall in 2013 - (Recall #: Z-2272-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia breathing circuit is a device that is intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Y-piece.

Product Classification:

Class I

Date Initiated: August 23, 2012

Date Posted: October 9, 2013

Recall Number: Z-2272-2013

Event ID: 66184

Reason for Recall:

King Systems received a customer complaint indicating that the customer had ordered a breathing circuit with a Latex breathing bag. The product they received contained a Latex breathing bag, but was labeled as non-latex.

Status: Terminated

Product Quantity: 1 case; 40 units

Code Information:

Part Number DF4110-61 Lot Number I063N

Distribution Pattern:

Nationwide Distribution - NE only.

Voluntary or Mandated:

Voluntary: Firm initiated