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.
Recall
- Recall Number
- Z-2272-2013
- Event Number
- 66184
- Firm
- King Systems Corp.
- FEI Number
- 1824226
- Product Code
- CAI
- Status
- Terminated
- Root Cause
- Labeling mix-ups
- Initiated
- August 23, 2012
- Posted
- September 27, 2013
- Terminated
- November 18, 2013
- Address
- 15011 Herriman Blvd, Noblesville, IN, 46060-4253
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.
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.
Ambu, Inc. sent a letter dated June 24, 2013, informing the customer that they have decided to discontinue the manufacture and sales of the King Systems latex breathing bags and to conver all customers to their King Systems latex-free breathing bags. The customer was advised to adjust their inventories accordingly and transition to the latex free part number as their inventory levels reach their minimums. For questions the customer was advised to call 317-403-8677. For questions regarding this recall call 317-776-6823.
Nationwide Distribution - NE only.
1 case; 40 units