Cincinnati Sub-Zero Products Inc: FDA recalls

FDA enforcement reports name Cincinnati Sub-Zero Products Inc as the recalling firm in 6 events. The events have 6 product records. The recalls started from 2013 to 2017. All the events are device recalls.

See the 6 events

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.

Enforcement events

6 events, newest first.

FDA enforcement events of Cincinnati Sub-Zero Products Inc
Initiated	Product (first record)	Type	Class	Records	Status
9 Mar 2017	Hemotherm CE, model 400CE, Heater-Cooling Device	Device	Class II	1	Terminated
7 Nov 2016	The Hemotherm 400CE 115v, containing power board p/n 39945	Device	Class II	1	Terminated
7 Jan 2015	Cold Therapy Pad - cold water circulating pad, one unit per package. The pads are used to provide a patient with local cold therapy by circulating chilled water through the pad that has been positioned on the patient.	Device	Class II	1	Terminated
8 Jan 2014	115 V Blanketrol II, Model 222S Hyper-Hypothermia System . Used to lower or to raise a patients temperature and /or maintain a desired patient temperature through conductive heat transfer. Part number 86165.	Device	Class II	1	Terminated
3 Sep 2013	Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241 Hyper-Hypothermia device used to lower or to raise a patient’s temperature and/or maintain a desired patient temperature through conductive heat transfer.	Device	Class II	1	Terminated
15 May 2013	Blanketrol III Data Export Software Version 1.10 The Blanketrol III Data Export Software is intended for use in the electronic transfer of medical device data from the Blanketrol III to a computer, without controlling or altering the function or parameters of the Blanketrol III.	Device	Class II	1	Terminated

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.

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Type and class

Cincinnati Sub-Zero Products Inc: events for each product type
Type		Events
Device		6

Cincinnati Sub-Zero Products Inc: events in each class
Class		Events
Class II		6

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: 0

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 Cincinnati Sub-Zero Products Inc, by the year that the recall started. The largest year is 2013, with 2 events.

Official channels

FDA enforcement reportsThe FDA search of the weekly enforcement reports.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA: report a problemThe FDA page that shows where a report about a product goes.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

Cite this page

Recall Register. Cincinnati Sub-Zero Products Inc: FDA recalls. https://recallregister.com/firm/cincinnati-sub-zero-products-inc/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

Sources

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

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 Cincinnati Sub-Zero Products Inc have?: Class II: 6 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 Cincinnati Sub-Zero Products Inc?: FDA event 76718, which the firm started on 9 Mar 2017. The first product in the record is: Hemotherm CE, model 400CE, Heater-Cooling Device
How many FDA recalls of Cincinnati Sub-Zero Products Inc have the status Ongoing?: No 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.