Quest Medical, Inc. FDA Recalls

2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets Class IIJul 14, 2023For administration of intravenous fluids to a patient s vasc	For administration of intravenous fluids to a patient s vascular system utilizing needle-free components and I	Class IIDevices	Jul 14, 2023
Precision Delivery Set with Filter, REF: PD06F; and Precision Delivery Set with Trifurcated Luer, REF: PDT05CV2Class IIDec 23, 2022Delivery Sets may have tubing that could become detached tha	Delivery Sets may have tubing that could become detached that could result in patient infection.	Class IIDevices	Dec 23, 2022