LifeGlobal® Media LGGG-050Recalls & reported problems
Lifeglobal Group, LLC · global 50 ml · Class 2
All models of LifeGlobal Media (5)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
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.
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
- Dec 20, 2023Class IIOpen, 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 · Recall details · FDA record ↗
Other MEDIA, REPRODUCTIVE devices
- Vit Kit® - Freeze 90133-SOFujifilm Irvine Scientific, Inc. · Media, Reproductive2 recalls0 reports
- LifeGlobal® Media H5GT-060Lifeglobal Group, LLC · MEDIA, REPRODUCTIVE1 recall0 reports
- LifeGlobal® Media LGGG-100Lifeglobal Group, LLC · MEDIA, REPRODUCTIVE1 recall0 reports
- LifeGlobal® Media LGGG-020Lifeglobal Group, LLC · MEDIA, REPRODUCTIVE1 recall0 reports
- ISolate® 99264-2x100mLFujifilm Irvine Scientific, Inc. · Media, Reproductive1 recall0 reports
- ORIGIO Sperm Wash 84050060DOrigio A/S · Media, Reproductive1 recall0 reports
- LifeGlobal® Media GFT5-055Lifeglobal Group, LLC · MEDIA, REPRODUCTIVE1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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