Device recall: Abbott Alinity ci-series System Control Module software version 2.5.1; LN 3R70-01 with the following hardware: Level…

Class II FDA enforcement event 82475. Recall start date: 7 Mar 2019. Status in the FDA record: Terminated. Termination date: 19 Feb 2025.

Reason for recall, in the words of FDA

Potential performance issues in the Alinity-ci software version 2.5.1

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

Abbott Gmbh & Co. KG started this device recall on 7 Mar 2019. The firm address in the FDA record is in Wiesbaden. FDA put the recall in Class II. FDA event 82475 has 1 product record. The first FDA enforcement report date is 22 May 2019. The record gives the status Terminated, with the termination date 19 Feb 2025.

FDA enforcement report The 1 product record

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 1 Oct 2026. openFDA export of 28 Sep 2026.

Distribution

In the words of FDA.

AR, AZ, CA, FL, GA, IL, MA, ME, MN, MO, NY, OK, SC, TN, TX, UT, VA, WI, and Puerto Rico ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BAHRAIN, BANGLADESH, BELGIUM, BOSNIA AND HERZEGOVINA, BRAZIL,…

Recalling firm

Abbott Gmbh & Co. KG, Wiesbaden, Germany.

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 82475: product records
Recall number	Product	Quantity	Class	Status	Report date
Z-1316-2019	Abbott Alinity ci-series System Control Module software version 2.5.1; LN 3R70-01 with the following hardware: Level Sensor, Bulk Solution; 04S68-01, Accessory Kit, Alinity I; 03R66-01and 03R66-02 , and Accessory Kit, Alinity c; 03R69-01 and 03R69-02. Product Usage: The Alinity i (LN 03R65 01) processing module is a…	1557	Class II	Terminated	22 May 2019

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 2019: 968
Share of these events in Class II: 88%
Product records in this event: 1Median of the firm: 1
Events of the firm on the register: 16

Other events of the firm

Other FDA enforcement events of Abbott Gmbh & Co. KG
Initiated	Product (first record)	Type	Class	Records
19 Jun 2020	Alinity ci series System Control Module (SCM); LN 3R70-01 Alinity ci series software versions, 3.1.1 and below	Device	Class II	1
12 May 2020	Alinity C, Processing Module. Chemistry analyzer for in-vitro diagnostics.	Device	Class II	1
24 Apr 2020	ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained are used in the diagnosis and treatment of	Device	Class II	1
9 Mar 2020	ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25.	Device	Class II	1
24 Jan 2020	LN 3R70-01; software version 2.6.2 and earlier. The software is used with the Alinity i (LN 03R65-01) processing module	Device	Class II	1
7 Nov 2019	ARCHITECT HAVAB-G Calibrator, REF 6L27-01	Device	Class II	1
23 Oct 2019	Alinity c Carbon Dioxide Reagent Kit, Produced for Abbott by Sekisui Diagnostics P.E.I. Inc. Prince Edward Island Canada	Device	Class II	1
16 Sep 2019	Alinity ci Level Sensor, Bulk Solution	Device	Class II	3
10 Jun 2019	Alinity ci -series System Control Module, Part Number 03R70 01 Product Usage: The Alinity ci series System Control Modul	Device	Class II	1
21 May 2019	The Alinity ci-series System Control Modules which are configured with Alinity c Processing Modules. The Alinity ci-seri	Device	Class II	1

Abbott Gmbh & Co. KG: all 16 events

Official channels

FDA enforcement report Z-1316-2019The FDA record of the first product of this event.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

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Cite this page

Recall Register. FDA enforcement event 82475. https://recallregister.com/fda/ii/82475/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

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: AR, AZ, CA, FL, GA, IL, MA, ME, MN, MO, NY, OK, SC, TN, TX, UT, VA, WI, and Puerto Rico ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BAHRAIN, BANGLADESH, BELGIUM, BOSNIA AND HERZEGOVINA, BRAZIL,…
What quantity of product is in FDA event 82475?: The FDA record gives this quantity: 1557
How did the recall start?: The FDA record says: Voluntary: Firm initiated
How many device recalls of 2019 have the same class?: 88% of the 968 device events that started in 2019 are in Class II.