Turkuaz recalls 50 units of sterile ultrasound gel (0.70 fl oz) due to potential sterility issues. Affected lots include SJ10091019 through SJ06022023. Consumers should check their lot numbers.
Sterility of Ultrasound gel can not be guaranteed.
Turkuaz is recalling 50 units of sterile ultrasound gel because the product may not be sterile. This could lead to infections if used in medical procedures. The recall affects specific lot numbers from the list provided.
The ultrasound gel may not be sterile, which could cause infections during medical procedures. This risk arises from the product's inability to maintain sterility as intended.
Medical professionals and patients using ultrasound gel for diagnostic purposes. Those with the listed lot numbers are most at risk.
Check the lot number on the product label. The affected lots are SJ10091019, SJ22111019, SJ01041120, SJ25081020, SJ25061020, SJ20111020, SJ11021021, SJ24061021, SJ03061021, SJ14071021, SJ20091021, SJ09091021, SJ06022023.
Look for the lot number on the ultrasound gel container to determine if it is affected.
The product may not be sterile, so it should not be used for medical procedures without confirming sterility.
Check the lot number on the product and contact Turkuaz for further instructions.
50 units of sterile ultrasound gel (0.70 fl oz) are being recalled.
We’ve drafted a message you can send Turkuaz to request your refund or repair — edit it as you like.
Subject: Recall Z-0777-2024 — Turkuaz Turkuaz Hello, I own a Turkuaz that is covered by recall Z-0777-2024 from Turkuaz. 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.
