FDA Device recall Z-1180-2016
Quick Connects
- FDA Device
- Class II
- terminated
- Published 2016-03-23
On 2016-03-23 the FDA classified a Class II recall of Quick Connects by Steris, citing the firm discovered that one of the hysteroscope models listed for processing in four existing Quick Connects has one inlet port rather than two inlet ports as indicated in the Qu….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1180-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-12-04 |
| Published | 2016-03-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Steris |
| Distribution | US |
Product
Quick Connects. Steris Corporation. Model numbers: QKC1736E, QKC1736INT, QKC1737E, and QKC1737INT. Each Quick Connect contains a flow unit consisting of tubing, tethers, and adapters. For sterilant and rinse water used in endoscope washers.
Reason
The firm discovered that one of the hysteroscope models listed for processing in four existing Quick Connects has one inlet port rather than two inlet ports as indicated in the Quick Connect processing instructions.
Identifiers
| code_info | All Lots. Model numbers: QKC1736E, QKC1736INT, QKC1737E, and QKC1737INT. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1180-2016%22
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