Anatomy Supply Partners recalls Safe-T-Fill 150μL blood gas capillary tubes with sodium heparin (model 06 0007) made between July 2023 and February 2025 due to unvalidated manufacturing processes.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners recalls Safe-T-Fill 150μL blood gas capillary tubes with sodium heparin (model 06 0007) produced from July 2023 to February 2025. These tubes were made using unvalidated manufacturing processes that could lead to quality issues.
The tubes were manufactured under an inadequate quality system with unvalidated processes. This could result in quality issues but does not indicate immediate danger to users.
Healthcare professionals and labs using these specific blood gas tubes for medical testing. Those with the model number 06 0007 produced between July 2023 and February 2025 are most at risk.
Check for the model number 06 0007 on the tube. Look for production dates between July 2023 and February 2025 (lots: 23I4008, 24D4024, 24D4155, 24E4126, 24E4127, 24E4287).
Identify the model number and production dates to confirm if the tube is part of the recall.
The product was manufactured under an inadequate quality system with unvalidated manufacturing processes.
Model 06 0007 produced from July 2023 to February 2025 (lots: 23I4008, 24D4024, 24D4155, 24E4126, 24E4127, 24E4287).
No immediate action is required; check the model and production dates to see if your tubes are affected.
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-0561-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0561-2026 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.
