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MEDRAD® Twist & Go Sterile High Pressure Connector Tubing, 120cm (48in)

BAYER MEDICAL CARE INC. · Model TAG C120 HPCT · UDI-DI 00616258006949

FPK Prescription

510(k) clearances

852

Adverse events (5 deaths)

Recalls

Facilities

Description

Twist & Go, HPCT, CoEx, 48'' (ANGIO - ART, HPCT, TWIST & GO, CO-EX, 48") (60766841)

Recalls

Date	Firm	Reason
2025-06-05	Merit Medical Systems, Inc.	High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may resu
2017-09-10	Medtronic Inc.	Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
2013-02-19	Hospira Inc.	Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore Extension Set, 59 inch with Spin Lock Collar, Non-DEHP, identified above due to a confirmed customer repor
2012-05-18	MOOG Medical Devices Group	Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu
2012-05-18	MOOG Medical Devices Group	Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu
2012-05-18	MOOG Medical Devices Group	Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu
2012-05-18	MOOG Medical Devices Group	Moog Medical Device Group became aware on March 23, 2011 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu
2012-05-18	MOOG Medical Devices Group	Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu
2012-05-18	MOOG Medical Devices Group	Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu
2012-05-18	MOOG Medical Devices Group	Moog Medical Device Group became aware on March 23, 2012 via customer complaint, of a reversed pump segment on an Administration Set. This malfunction could reverse the flow of flu

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.