LifeGlobal® Media H5GT-060Recalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

1 other recall cover devices cleared under the same FDA submission (K142991); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Feb 13, 2023Class IIOpen, Classified

   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.

   Z-1348-2023 · Root cause: Labeling Change Control · Recall details · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K142991. One submission often covers many models, so check the product and lot details in each record.

• Z-1089-2024 · Dec 20, 2023 · Open, Classified
  global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use: Culture of human embryos from zygote to blastocyst, embryo trans