Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection devices (model 07 7151) due to unvalidated manufacturing processes. 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 devices (model 07 7151) 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 devices 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.
People who own or use SAFE-T-FILL Micro Capillary Blood Collection devices with model number 07 7151. Healthcare providers and individuals using these devices for blood collection are most at risk.
Check for model number 07 7151 on the device. Affected units were produced from August 2023 to February 2025 with specific lot numbers: 24I4329, 24J4346, 25B4105.
Look for model number 07 7151 on the device label.
Contact Anatomy Supply Partners for further instructions if you have the affected model.
The product was manufactured under an inadequate quality system that included unvalidated manufacturing processes.
Model number 07 7151 with specific lot numbers: 24I4329, 24J4346, 25B4105.
The recall does not specify a safety hazard; it focuses on inconsistent product quality due to manufacturing issues.
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-0548-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0548-2026 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.
