Recall Register

Accelerate Diagnostics Inc: FDA recalls

FDA enforcement reports name Accelerate Diagnostics Inc as the recalling firm in 3 events. The events have 4 product records. The recalls started from 2017 to 2022. All the events are device recalls.

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 .

Enforcement events

3 events, newest first.

FDA enforcement events of Accelerate Diagnostics Inc
InitiatedProduct (first record)TypeClassRecordsStatus
17 Oct 2022Accelerate PhenoTest BC kit REF 10101018DeviceClass II2Ongoing
14 Mar 2018Accelerate PhenoTest BC kit, Ref #10101018. The firm name on the label is Accelerate Diagnostics, Tucson, AZ. A multiplexed in-vitro diagnostic test intended for use with the Accelerate Pheno system.DeviceClass II1Terminated
13 Mar 2017Accelerate Pheno system, with Accelerate Pheno System Software 1.2.1 - 1.3.1, PSW000012B Product Usage: The Accelerate Pheno system is intended to measure signal intensity of fluorescent probes bound to nucleic acid in target and non-target organisms and to take time-lapse dark-field images of immobilized growing…DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

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

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

Type and class

Accelerate Diagnostics Inc: events for each product type
TypeEvents
Device3
Accelerate Diagnostics Inc: events in each class
ClassEvents
Class II3
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
1

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.

Events by year

FDA enforcement events of Accelerate Diagnostics Inc, by the year that the recall started. The largest year is 2017, with 1 event.

Official channels

Cite this page

Recall Register. Accelerate Diagnostics Inc: FDA recalls. https://recallregister.com/firm/accelerate-diagnostics-inc/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
AZ

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Accelerate Diagnostics Inc have?
Class II: 3 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Accelerate Diagnostics Inc?
FDA event 91075, which the firm started on 17 Oct 2022. The first product in the record is: Accelerate PhenoTest BC kit REF 10101018
How many FDA recalls of Accelerate Diagnostics Inc have the status Ongoing?
1 event has the status Ongoing in the openFDA file. openFDA says 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.