Anatomy Supply Partners recalls SAFE-T-FILL Plastic Blood Gas Capillary Tubes (Model 06 0185) manufactured from July 2023 to February 2025 due to unvalidated manufacturing processes. Affected units may have quality issues.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling SAFE-T-FILL Plastic Blood Gas Capillary Tubes (Model 06 0185) made between July 2023 and February 2025 because they were produced under an inadequate quality system. This could lead to potential quality issues with the tubes.
The tubes were manufactured under an inadequate quality system, which means unvalidated manufacturing processes could result in quality issues. This might affect the accuracy or reliability of blood gas tests.
Healthcare professionals and labs using these tubes for blood gas testing are most at risk. The recall affects units produced from July 2023 through February 2025.
Check for the model number 06 0185 on the tube. The product was sold from July 2023 to February 2025 with specific lot numbers: 23I4061, 24D4022, 24F4009, 24F4186.
Look for the model number 06 0185 and lot numbers 23I4061, 24D4022, 24F4009, or 24F4186 on the tube.
The tubes were manufactured under an inadequate quality system, which includes unvalidated manufacturing processes.
Check for model number 06 0185 on the tube.
The tubes were produced from July 2023 through February 2025.
No specific stop-use instruction is provided; the recall is for quality assurance.
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-0563-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0563-2026 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.
