CooperSurgical, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0488-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class III

Date Initiated: October 27, 2014

Date Posted: December 10, 2014

Recall Number: Z-0488-2015

Event ID: 69642

Reason for Recall:

The product has been identified to contain an incorrect curette type.

Status: Terminated

Product Quantity: 30

Code Information:

Lot Code: 147234

Distribution Pattern:

US Distribution including the states of NY, MO and NV.

Voluntary or Mandated:

Voluntary: Firm initiated