Abbott Alinity M System: FDA Investigation Launched?

Dec 9, 2022 · fda determined cause 2: On december 09, 2022, abbott molecular issued a field correction recall/urgent field safety notice to all customers who have the. Jun 12, 2024 · the alinity m hr hpv is a laboratory test used to detect human papillomavirus (hpv) genetic material, or viral dna, in samples taken from the lower part of a patient’s uterus. Alinity m uses polymerase chain reaction (pcr). Oct 12, 2022 · abbott has identified potential performance issues for the alinity m system software version 1. 6. 5:

This issue has been observed with copan utm. On september 17, 2021, the u. s. Food and drug administration (fda) issued a letter to clinical laboratory staff and health care providers about false positive results that can occur with the. Abt) has received u. s. Food and drug administration (fda) approval for its molecular human papillomavirus or hpv screening. Under investigation by firm action the field service engineer installed the missing plunger assembly in the clamp bar while at the consignee location on 11/11/2022.