Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection devices (model 07 7150) 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 their SAFE-T-FILL Micro Capillary Blood Collection devices (model 07 7150) because they were made using unvalidated manufacturing processes. This could lead to inconsistent product quality, but the recall does not specify a direct safety risk to users.
The products were manufactured under an inadequate quality system that included unvalidated manufacturing processes. This could result in inconsistent product quality, but the recall does not indicate a specific safety hazard like injury or malfunction.
Healthcare professionals and individuals using capillary blood collection devices for testing. Those most at risk are users who have the specific model number 07 7150.
Check for the model number 07 7150 on the device. The product was sold from August 2023 to February 2025 with specific lot numbers: 23I4024, 24B4196, 24H4129, 24J4135, 24J4345, 25B4104.
Look for the model number 07 7150 and lot numbers 23I4024, 24B4196, 24H4129, 24J4135, 24J4345, or 25B4104 on the device packaging.
The recall states the products were made with unvalidated manufacturing processes, but it does not mention any specific safety hazard like injury or malfunction.
The recall does not provide a remedy, so no action is required beyond checking if your product matches the described model and lot numbers.
These products were manufactured from August 2023 to 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-0547-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0547-2026 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.
