Anatomy Supply Partners recalls SAFE-T-FILL MicroHematocrit Capillary Tubes (Model 06 0508) due to inadequate quality control during manufacturing. These tubes were produced from August 2020 to February 2025 and may have unvalidated manufacturing processes.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling SAFE-T-FILL MicroHematocrit Capillary Tubes with blue markings and model number 06 0508. The recall is due to manufacturing issues that could affect product quality, though no specific safety risks are mentioned in the recall notice.
The tubes were manufactured under an inadequate quality system, which may include unvalidated manufacturing processes. This could lead to inconsistent product quality but does not indicate a direct safety risk like injury or malfunction.
Users of medical capillary blood collection tubes, particularly those in healthcare settings or labs that use these specific tubes. The risk is low as the recall focuses on quality control rather than immediate safety hazards.
Check for blue markings and model number 06 0508 on the tubes. These tubes were produced from August 2020 through February 2025 and may have lot numbers starting with 21F4062 to 24J4350.
Identify if your tubes have blue markings and model number 06 0508.
The recall is due to manufacturing under an inadequate quality system that may include unvalidated processes, but no specific safety risks are mentioned.
The recall notice does not specify a remedy, so you can continue using them if they are functioning properly.
These tubes were produced from August 2020 through 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-0556-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0556-2026 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.
