Aquabiliti recalls 5mL and 3mL saline syringes that may not meet USP sodium chloride content standards after 12 months. Affected units include specific lot numbers and expiration dates.
The saline flush syringes may fail to meet USP criteria for stated sodium chloride content after 12 months.
Aquabiliti is recalling saline injection syringes that could have inaccurate sodium chloride content after 12 months. This means the salt concentration might be too low, which could affect medical treatments if used improperly.
The syringes may not meet USP standards for sodium chloride content after 12 months. This could lead to incorrect salt levels in medical treatments, potentially causing treatment errors if used without proper verification.
Healthcare professionals and patients using these saline syringes for medical treatments. Those who have the specific lot numbers and expiration dates listed in the recall are most at risk.
Check for the product name 'AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe, USP' with specific lot numbers and expiration dates listed in the recall notice.
Look for the lot numbers and expiration dates listed in the recall notice to confirm if your syringes are affected.
The recall states the syringes may not meet USP standards for sodium chloride content after 12 months, so they should not be used without verification.
Check the lot numbers and expiration dates against the list provided in the recall notice. If affected, stop using and contact Aquabiliti for further instructions.
Look for the specific lot numbers and expiration dates listed in the recall notice for the 5mL and 3mL syringes.
We’ve drafted a message you can send Aquabiliti to request your refund or repair — edit it as you like.
Subject: Recall Z-1174-2024 — Aquabiliti Aquabiliti Hello, I own a Aquabiliti that is covered by recall Z-1174-2024 from Aquabiliti. 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.
