Anatomy Supply Partners recalls 230μL blood gas capillary tubes with sodium heparin due to inadequate quality control during manufacturing. Affected lots produced from July 2023 to February 2025.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling blood gas capillary tubes that may have been made with unvalidated manufacturing processes. This could lead to quality issues with the tubes, though serious injury risks aren't specified in the recall notice.
The tubes were manufactured under an inadequate quality system that included unvalidated processes. This could result in inconsistent quality, but the recall does not specify a risk of serious injury or death.
Healthcare professionals using these tubes for blood gas testing are likely affected. Patients receiving blood tests using these tubes may be at risk if the tubes have quality issues.
Check for model number 06 0009 on the tube packaging. The product was sold from July 2023 to February 2025 with specific lot numbers: 23H4156, 23I4015, 24B4198, 24F4187, 24I4313, 24J4133.
Look for lot numbers 23H4156, 23I4015, 24B4198, 24F4187, 24I4313, or 24J4133 on the tube packaging.
The recall states the tubes were made with unvalidated manufacturing processes, but does not specify that they are unsafe for use. Users should check the lot number to determine if they are affected.
The recall does not provide a specific remedy, so users should check the lot number to see if they are affected. If affected, they may need to contact the manufacturer for further instructions.
The tubes were produced from July 2023 to February 2025.
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-0562-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0562-2026 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.
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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.
