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

Recall Z-1461-2018 — Cook Vacuum Pump ( Cook Aspiration Unit) K-MAR-5200-US, GPN G49275. Intended for the aspiration of body fluids and cells, in particular oocyte aspiration.

U.S. FDA — Device Enforcement · United States · 2018-03-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1461-2018
Date of alert: 2018-03-22
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Cook Inc.
Product category: device
Product type: Devices

Reported risk: Pump was found to be constructed from crimp connectors that do not meet the fixation wiring requirements and can cause failure of the device to operate or electric shock or burn to the user.

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

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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.

Recall Z-1461-2018 — Cook Vacuum Pump ( Cook Aspiration Unit) K-MAR-5200-US, GPN G49275. Intended for the aspiration of body fluids and cells, in particular oocyte aspiration.

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