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King Systems Corp. recalls Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia breathing circuit is a device that is intend
Recalled October 9, 2013 · FDA recall Z-2272-2013 · King Systems
Hazard
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. · FDA Class I
Units
1 case; 40 units
Sold at
Nationwide Distribution - NE only.
Description
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.
Product
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.
Manufacturer(s)
King Systems Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →