FDA Device recall Z-1129-2015
Cold Therapy Pad - cold water circulating pad, one unit per package
- FDA Device
- Class II
- terminated
- Published 2015-02-25
On 2015-02-25 the FDA classified a Class II recall of Cold Therapy Pad - cold water circulating pad, one unit per package by Cincinnati Sub Zero Products, citing seals in the water path of the CT-99 cold therapy pad may separate during use, which could lead to a water leak.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1129-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-07 |
| Published | 2015-02-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Cincinnati Sub Zero Products |
| Distribution | US |
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.
Reason
Seals in the water path of the CT-99 cold therapy pad may separate during use, which could lead to a water leak.
Identifiers
| code_info | Model: Catalog #CT -99 Part number: 50137 Lot number(s): 13380, 13390 and 13418. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1129-2015%22
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