Cooper Surgical CANNULA-CURETTE 12MM — Class III medical device recall Z-0488-2015
Terminated recall by CooperSurgical, Inc., reported 2014-12-10, distributed in MO, NV, NY. The product has been identified to contain an incorrect curette type.
| Recall number | Z-0488-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2014-10-27 |
| Classified | 2014-12-01 |
| Reported by FDA | 2014-12-10 |
| Terminated | 2015-05-28 |
| Distributed | MO, NV, NY |
| Quantity | 30 |
| Lot numbers | 147234 |
| Model numbers | MX562 |
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 for recall
The product has been identified to contain an incorrect curette type.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0488-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.