FDA Device recall Z-0488-2015
Cooper Surgical CANNULA-CURETTE 12MM
- FDA Device
- Class III
- terminated
- Published 2014-12-10
On 2014-12-10 the FDA classified a Class III recall of Cooper Surgical CANNULA-CURETTE 12MM by Coopersurgical, citing the product has been identified to contain an incorrect curette type.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0488-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-10-27 |
| Published | 2014-12-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Coopersurgical |
| Distribution | MO, NV, NY |
Product
Cooper Surgical CANNULA-CURETTE 12MM; Model Number: MX562 The CooperSurgical SUCTION CANNULA-CURETTE device is used to remove tissue from within the uterine cavity on an outpatient basis. The primary uses for this device are for endometrial sampling especially of those patients with a higher risk of cancer. The curettes must be used with a suction pump, as well as sterile tubing, and a swivel handle. The rigid plastic suction curette is sterile and disposable. The Cannula Curette is available in the following styles: Long Curved, Long Straight, and Short Curved.
Reason
The product has been identified to contain an incorrect curette type.
Identifiers
| code_info | Lot Code: 147234 |
|---|
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-0488-2015%22
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