Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0488-2015 — 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

U.S. FDA — Device Enforcement · United States · 2014-10-27 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0488-2015
Date of alert: 2014-10-27
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: CooperSurgical, Inc.
Product category: device
Product type: Devices

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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