Skip to content

LifeGlobal MediaRecalls & reported problems across all models

Lifeglobal Group, LLC · 5 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

3 open recalls name at least one LifeGlobal Media model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls
3

We found 5 models of LifeGlobal Media by Lifeglobal Group, LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

3 FDA recall records name at least one of these models by its device identifier, 3 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

LifeGlobal Media recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. Dec 20, 2023Open, Classified

    The firm has become aware of a sudden increase in complaints for three associated lots. Performance issues may lead to impaired embryo development prior to the blastocyst stage.

    Z-1089-2024 · Root cause: Under Investigation by firm · names 3 of these models · Recall details · FDA record ↗

  2. Feb 13, 2023Open, 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 ↗

  3. Jun 13, 2022Open, Classified

    There was translation error in the Spanish version of the IFU where the Spanish version instructs the user to leave the blastocyte to air thaw for 5 minutes rather than the correct 5 seconds as indicated in the English version.

    Z-1421-2022 · Root cause: Error in labeling · Recall details · FDA record ↗

LifeGlobal Media models

5 models, most reported first. Each model has its own page with its reports, recalls and device details.

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page