Anatomy Supply Partners recalls 115μL blood gas capillary tubes with sodium heparin (model 06 0005) made from July 2023 to February 2025 due to inadequate quality control. Affected units may have manufacturing defects.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling blood gas capillary tubes that were made between July 2023 and February 2025. The recall is because these tubes were produced using unvalidated manufacturing processes that could lead to quality issues.
The tubes were manufactured under an inadequate quality system, which means the production process wasn't validated properly. This could result in tubes that don't meet quality standards, but it doesn't pose an immediate risk of injury or harm.
Healthcare professionals and labs using these tubes for blood gas testing are most likely affected. The risk is low as the hazard relates to potential quality issues rather than immediate safety risks.
Check for the model number 06 0005 on the tube. The tubes were produced from July 2023 through February 2025 and come in a clear plastic form with sodium heparin.
Look for the model number 06 0005 on the tube and verify the production dates (July 2023 to February 2025).
The recall indicates potential quality issues due to unvalidated manufacturing processes, but the tubes are not unsafe for use in normal conditions.
Check for the model number 06 0005 and production dates from July 2023 to February 2025.
The recall does not specify a remedy, so you can continue using them if they are in good condition.
We’ve drafted a message you can send Anatomy Supply Partners to request your refund or repair — edit it as you like.
Subject: Recall Z-0560-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0560-2026 from Anatomy Supply Partners. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
