Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1129-2015 — 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.

U.S. FDA — Device Enforcement · United States · 2015-01-07 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1129-2015
Date of alert: 2015-01-07
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Cincinnati Sub-Zero Products Inc
Product category: device
Product type: Devices

Reported risk: Seals in the water path of the CT-99 cold therapy pad may separate during use, which could lead to a water leak.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Recall Z-1129-2015 — 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.

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