FDA Device recall Z-1320-2022

Mahurkar Chronic Carbothane (Maxid) Catheter, Sterile, Single Use, Rx Only

FDA Device
Class I
ongoing
Published 2022-07-13

On 2022-07-13 the FDA classified a Class I recall of Mahurkar Chronic Carbothane (Maxid) Catheter, Sterile, Single Use, Rx Only by Covidien, citing there is a potential leaking condition within the hub of specific chronic dialysis catheters, due to an inter-lumen void in the hub component, which may result in unanticipated fl….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1320-2022
Classification	Class I
Status	ongoing
Initiated	2022-06-08
Published	2022-07-13
Last updated	2026-09-13 11:56 UTC
Company	Covidien
Distribution	US

Product

Mahurkar Chronic Carbothane (Maxid) Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.

Reason

There is a potential leaking condition within the hub of specific chronic dialysis catheters, due to an inter-lumen void in the hub component, which may result in unanticipated fluid return during use.

Identifiers

code_info	Code Information organized as "Model No., Serial No., GTIN": 8888119362, 1928800230, 10884521056879; 8888119362, 182540… Code Information organized as "Model No., Serial No., GTIN": 8888119362, 1928800230, 10884521056879; 8888119362, 1825400094, 20884521056876; 8888119362, 1912600107, 20884521056876; 8888119362, 1917600139, 20884521056876; 8888119362, 1917700080, 20884521056876; 8888119362, 1925200098, 20884521056876; 8888119362, 1927300146, 20884521056876; 8888119362, 1928800230, 20884521056876; 8888119362, 2023300144, 20884521056876; 8888119362, 2028200216, 20884521056876; 8888119362, 2122900239, 20884521056876; 8888119385, 1720700105, 20884521012421; 8888119385, 1724900109, 20884521012421; 8888119385, 2113300429, 20884521012421; 8888123402, 1927500121, 10884521056886; 8888123402, 2028200203, 10884521056886; 8888123402, 2110900059, 10884521056886; 8888123402, 1921700145, 20884521056883; 8888123402, 1924000138, 20884521056883; 8888123402, 1925200091, 20884521056883; 8888123402, 1927500120, 20884521056883; 8888123402, 1927500121, 20884521056883; 8888123402, 2023300143, 20884521056883; 8888123402, 2026000

code_info

Code Information organized as "Model No., Serial No., GTIN": 8888119362, 1928800230, 10884521056879; 8888119362, 182540…

Code Information organized as "Model No., Serial No., GTIN": 8888119362, 1928800230, 10884521056879; 8888119362, 1825400094, 20884521056876; 8888119362, 1912600107, 20884521056876; 8888119362, 1917600139, 20884521056876; 8888119362, 1917700080, 20884521056876; 8888119362, 1925200098, 20884521056876; 8888119362, 1927300146, 20884521056876; 8888119362, 1928800230, 20884521056876; 8888119362, 2023300144, 20884521056876; 8888119362, 2028200216, 20884521056876; 8888119362, 2122900239, 20884521056876; 8888119385, 1720700105, 20884521012421; 8888119385, 1724900109, 20884521012421; 8888119385, 2113300429, 20884521012421; 8888123402, 1927500121, 10884521056886; 8888123402, 2028200203, 10884521056886; 8888123402, 2110900059, 10884521056886; 8888123402, 1921700145, 20884521056883; 8888123402, 1924000138, 20884521056883; 8888123402, 1925200091, 20884521056883; 8888123402, 1927500120, 20884521056883; 8888123402, 1927500121, 20884521056883; 8888123402, 2023300143, 20884521056883; 8888123402, 2026000

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1320-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.