Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection tubes (Green Model 07) due to inadequate quality control during manufacturing. Affected units were produced from August 2023 to February 2025.
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 tubes (Green Model 07) because they were made using unvalidated manufacturing processes. This could lead to inconsistent product quality, but the recall does not specify immediate safety risks.
The tubes were manufactured using unvalidated processes that may not meet quality standards. This could result in inconsistent performance, but the recall does not indicate a specific safety hazard like injury or malfunction.
People who own or use SAFE-T-FILL Micro Capillary Blood Collection tubes with Green Model/Catalog Number 07. Healthcare professionals and individuals using these tubes for blood collection are most at risk.
Check for the Green Model/Catalog Number 07 on the tube. Affected units were produced from August 2023 to February 2025 with lot numbers 24K4001 or 25B4102.
Look for the Green Model/Catalog Number 07 and lot numbers 24K4001 or 25B4102 on the tube.
The product was manufactured using unvalidated processes that may not meet quality standards.
Check the product details to see if it matches the recalled model and lot numbers. No specific action is required beyond checking.
The recall does not indicate a specific safety hazard like injury or malfunction.
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-0552-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0552-2026 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.
