Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection tubes (model 07 7450) produced from August 2023 to February 2025 due to inadequate quality control. Consumers should contact the company 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 tubes (model 07 7450) produced from August 2023 to February 2025 because of quality control issues. This recall affects people who use these blood collection tubes for finger or heelstick blood draws.
The recall states that the products were made under an inadequate quality system with unvalidated manufacturing processes. This could lead to inconsistent product performance, but the specific risk to users is not clearly described in the recall.
People who use SAFE-T-FILL Micro Capillary Blood Collection tubes for blood draws are affected. Those with medical conditions requiring frequent blood tests may be at higher risk.
Check for the model number 07 7450 on the tube packaging. The product was manufactured from August 2023 to February 2025. The lot number 23H4158 is associated with this recall.
Reach out to Anatomy Supply Partners for specific instructions on how to handle the recalled product.
The recall states that the products were made under an inadequate quality system, but does not specify if they are safe to use.
Look for the model number 07 7450 on the tube packaging and check the production dates from August 2023 to February 2025.
Contact Anatomy Supply Partners for specific instructions on how to handle the recalled product.
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-0554-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0554-2026 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.
