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

Recall Z-1348-2023 — Global Total LP single step medium, 60mL, bicarbonate-buffered media for D1-5 embryo culture and transfer, Reference Number H5GT-060

U.S. FDA — Device Enforcement · United States · 2023-02-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1348-2023
Date of alert
2023-02-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CooperSurgical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00815965020433
Reported risk: It has come to CooperSurgical's attention that the affected Product may contain a medium other than the Global Total LP single step medium which does not contain the protein source required for embryo culture and development.
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.

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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.