Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection tubes due to inadequate quality control during manufacturing, potentially affecting blood collection safety.
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 because they were made using unvalidated manufacturing processes. This could lead to improper blood collection if the tubes are used without proper quality assurance.
The tubes were manufactured under an inadequate quality system that included unvalidated manufacturing processes. This could result in improper blood collection if the tubes are used without proper quality assurance, potentially leading to inaccurate test results or safety issues.
People who own or use SAFE-T-FILL Micro Capillary Blood Collection tubes with model number 07 7221, produced from August 1, 2023, to February 28, 2025, are affected. Healthcare professionals and individuals using these tubes for blood collection are most at risk.
Check for the model number 07 7221 on the tube packaging. The tubes were produced from August 1, 2023, to February 28, 2025, and have a green color with lithium heparin and plasma separator gel.
Identify the model number 07 7221 on the tube packaging to confirm if it is affected.
The product was manufactured under an inadequate quality system that included unvalidated manufacturing processes.
The recall does not specify a remedy, so check the product details to determine if it is affected.
The recall indicates a potential risk due to manufacturing issues, but specific safety hazards are not detailed.
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-0550-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0550-2026 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.
