Anatomy Supply Partners recalls Model 07 9503 SAFE-T-FILL Blood Gas Capillaries produced from February 2023 to February 2025 due to unvalidated manufacturing processes. Affected units include specific lot numbers.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling Model 07 9503 SAFE-T-FILL Blood Gas Capillaries made between February 2023 and February 2025. The recall is due to unvalidated manufacturing processes that could affect product quality.
The capillaries were manufactured under an inadequate quality system with unvalidated processes. This could lead to inconsistent product quality but does not pose an immediate risk of injury or failure during normal use.
Healthcare professionals using these capillaries for blood gas testing are likely affected. The risk is low as the hazard relates to manufacturing quality rather than immediate safety concerns.
Check for the model number 07 9503 on the capillaries. The affected units were produced from February 2023 to February 2025 and include specific lot numbers listed in the recall notice.
Identify the model number 07 9503 and check if your capillaries were produced between February 2023 and February 2025.
The product was manufactured under an inadequate quality system with unvalidated manufacturing processes.
Check the model number and production dates to see if it's affected. If it is, contact the manufacturer for further instructions.
The recall is due to potential quality issues but does not pose an immediate safety risk during normal use.
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-0566-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0566-2026 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.
