CLASS II Device recall · Reported 12 Mar 2014 · FDA Enforcement Report

Meditech Microbiology - Calculator/data processing module recalled

Medical Information Technology is recalling Meditech Microbiology - Calculator/data processing module, for clinical use, distributed nationwide in the US. The recall was initiated on 17 Jan 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel, catalogue, or product order number(s): MAGIC Releases 5.6, 5. 5.66 and Server Releases 5.6, 5.65. 6.0, 6.05, 6.06, 6.07, 6.1 and 6.13.
Quantity recalled737

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1124-2014
FDA event ID
67458
Recalling firm
Medical Information Technology, Canton, MA
Classification
Class II
Status
Terminated
Recall initiated
17 Jan 2014
FDA classified
3 Mar 2014
Reported
12 Mar 2014
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons

Timeline

17 Jan 2014Recall initiated by company
3 Mar 2014Classified by FDA+45 days
12 Mar 2014Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential for patient results being removed from LAB/EMR.

Product as listed by the FDA

MEDITECH Microbiology - Calculator/data processing module, for clinical use.

Where it was distributed

Worldwide Distribution: US (nationwide) and to countries of: Canada, Ireland, and United Kingdom.

Nationwide

Questions about this recall

Why was it recalled?

Potential for patient results being removed from LAB/EMR.

Which lots are affected?

Model, catalogue, or product order number(s): MAGIC Releases 5.6, 5. 5.66 and Server Releases 5.6, 5.65. 6.0, 6.05, 6.06, 6.07, 6.1 and 6.13.

Where was it sold?

Worldwide Distribution: US (nationwide) and to countries of: Canada, Ireland, and United Kingdom.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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