Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection devices (Green Model 07) due to inadequate quality control during manufacturing. Affected units were produced from August 2023 to February 2025. Consumers should contact the manufacturer for details.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling SAFE-T-FILL Micro Capillary Blood Collection devices (Green Model 07) because they were made using unvalidated manufacturing processes. This could lead to improper blood collection if the device fails during use.
The devices were manufactured under an inadequate quality system, meaning the production processes weren't properly validated. This could result in the device failing during blood collection, potentially causing inaccurate results or minor issues.
People who own or use SAFE-T-FILL Micro Capillary Blood Collection devices (Green Model 07) for blood draws are affected. Those with the specific model and production dates listed are most at risk.
Check for the Green Model 07 with Catalog Number 07. Affected units were produced from August 2023 to February 2025 with specific lot numbers listed in the recall notice.
Reach out to Anatomy Supply Partners for details about the recall and any necessary steps to address the issue.
SAFE-T-FILL Micro Capillary Blood Collection devices (Green Model 07) with Catalog Number 07.
From August 2023 to February 2025.
Look for the Green Model 07 with Catalog Number 07 and check if it was produced between August 2023 and February 2025 with the listed lot numbers.
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-0544-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0544-2026 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.
