CooperSurgical recalls three embryo culture bottle models (20mL, 50mL, 100mL) after reports of impaired embryo development. Affected units may need replacement to prevent issues during early embryonic growth.
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.
CooperSurgical is recalling three sizes of embryo culture bottles (20mL, 50mL, 100mL) because some units may cause embryo development problems before the blastocyst stage. This could affect fertility treatments if the bottles are used improperly.
The bottles may cause impaired embryo development during the early stages of growth, specifically before the blastocyst stage. This could lead to issues with fertility treatments if the bottles are used without proper quality control.
Individuals using these embryo culture bottles for in vitro fertilization treatments are likely affected. Those with recent embryo transfers using the recalled models are at higher risk.
Check for model numbers LGGG-020 (20mL), LGGG-050 (50mL), or LGGG-100 (100mL) on the bottle. The recall covers specific production lots with UDI-DI numbers 00815965020044, 00815965020051, and 00815965020068.
Identify the model number on the bottle to see if it matches LGGG-020, LGGG-050, or LGGG-100.
The recall reports a sudden increase in complaints about impaired embryo development before the blastocyst stage.
Check for model numbers LGGG-020 (20mL), LGGG-050 (50mL), or LGGG-100 (100mL) with UDI-DI numbers 00815965020044, 00815965020051, or 00815965020068.
The recall does not specify a stop-use action, so you can continue using them if they are not the affected model numbers.
We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1089-2024 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-1089-2024 from CooperSurgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
