The Recall Desk

Manufacturer

Cincinnati Sub-Zero Products Inc

6 recalls in our database name Cincinnati Sub-Zero Products Inc as the manufacturing or recalling firm.

What the numbers show

Total
6
Critical
0
Severe
0
Most recent
2017-04-26

Of the 6 recalls from Cincinnati Sub-Zero Products Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–6 of 6

  • ModerateFDA (Devices)·Z-1129-2015·2015-02-25

    Cincinnati Sub-Zero CT-99 Cold Therapy Pad Recall for Seal Separation

    Cincinnati Sub-Zero is recalling CT-99 cold therapy pads because seals may separate during use, causing water leaks.

    Product
    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.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1679-2014·2014-06-11

    Cincinnati Sub-Zero Recalls 115 V Blanketrol II Hyper-Hypothermia Systems

    Cincinnati Sub-Zero is recalling seven 115 V Blanketrol II Hyper-Hypothermia Systems due to an incorrect voltage component that may prevent the device from maintaining patient temperature during cooling.

    Product
    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.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0443-2014·2013-12-11

    Cincinnati Sub-Zero Recalls Blanketrol III Data Export Software Version 1.10

    Cincinnati Sub-Zero Products Inc is recalling 12 units of Blanketrol III Data Export Software Version 1.10 because the wrong software version was released to a customer.

    Product
    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 II
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2209-2013·2013-09-25

    Cincinnati Sub-Zero Blanketrol III Manuals Recalled for Labeling Error

    Cincinnati Sub-Zero is recalling Blanketrol III manuals because text was incorrectly added back, contradicting the device's approved intended use.

    Product
    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 patients temperature and/or maintain a desired patient temperature through conductive heat transfer.
    Category
    Medical Device
    Distribution
    41 states