King Systems Corp. King Systems 72" Universal Flex2 Extension Kit, 50 per case, King Systems Corporation, Noblesville, IN; REF # XF75. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
King Systems 72" Universal Flex2 Extension Kit, 50 per case, King Systems Corporation, Noblesville, IN; REF # XF75.
Brand
King Systems Corp.
Lot Codes / Batch Numbers
Lots IKAE1, IKCJ4, IKER6, IKGC0, IKIJ7, IKJK6, IKMI3, IKQ81, IKUX4, IKVS2, IKY06, IL161, IL1Y6, IL383, IL7N9 and IL8Y9.
Products Sold
Lots IKAE1, IKCJ4, IKER6, IKGC0, IKIJ7, IKJK6, IKMI3, IKQ81, IKUX4, IKVS2, IKY06, IL161, IL1Y6, IL383, IL7N9 and IL8Y9.
King Systems Corp. is recalling King Systems 72" Universal Flex2 Extension Kit, 50 per case, King Systems Corporation, Noblesville, due to The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated pa. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Recommended Action
Per FDA guidance
Consignees were notified by an Urgent Product Recall letter on or about 7/29/2008 to cease sales, notify their customers to the hospital level, and to return product on hand.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026