Recall Register

Device recall: VITROS CHEMISTRY PRODUCTS TRIG Slides, REF 133 6544, IVD For in vitro diagnostic use only. VITROS Chemistry Products…

Class II FDA enforcement event 69791. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Potential for biased results using the specific lot of VITROS CHEMISTRY PRODUCTS TRIG slides.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Ortho-Clinical Diagnostics started this device recall on 6 Nov 2014. The firm address in the FDA record is in Rochester, NY. FDA put the recall in Class II. FDA event 69791 has 1 product record. The first FDA enforcement report date is 31 Dec 2014. The record gives the status Terminated, with the termination date 28 Feb 2017.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Worldwide Distribution - USA (nationwide) Puerto Rico and Internationally to Australia, Brazil, Canada, Chile, China, Colombia, England, France, Germany, India, Italy, Japan, Mexico, Panama,…

Recalling firm

Ortho-Clinical Diagnostics, Rochester, NY.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 69791: product records
Recall numberProductQuantityClassStatusReport date
Z-0848-2015VITROS CHEMISTRY PRODUCTS TRIG Slides, REF 133 6544, IVD For in vitro diagnostic use only. VITROS Chemistry Products TRIG Slides quantitatively measure triglyceride (TRIG) concentration in serum and plasma using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System.USA: 380 units, Foreign: 155 unitsClass IITerminated31 Dec 2014

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2014
1,176
Share of these events in Class II
91%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
105

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 69791. https://recallregister.com/fda/ii/69791/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Worldwide Distribution - USA (nationwide) Puerto Rico and Internationally to Australia, Brazil, Canada, Chile, China, Colombia, England, France, Germany, India, Italy, Japan, Mexico, Panama,…
What quantity of product is in FDA event 69791?
The FDA record gives this quantity: USA: 380 units, Foreign: 155 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2014 have the same class?
91% of the 1,176 device events that started in 2014 are in Class II.