LifeGlobal® Media GFT5-055Recalls & reported problems
Lifeglobal Group, LLC · global Blastocyst Fast Freeze Thawing kit, 5ml vials.. · 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
- Jun 13, 2022Class IIOpen, 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 ↗
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-050Lifeglobal 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
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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