Anatomy Supply Partners recalls 150μL blood gas capillary tubes with unvalidated manufacturing processes. Affected lots produced from July 2023 to February 2025. No remedy specified in recall notice.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling certain blood gas capillary tubes due to unvalidated manufacturing processes. This could lead to quality issues with the tubes, though the specific risk is not detailed in the recall notice.
The tubes were manufactured using unvalidated processes that may not meet quality standards. This could result in inconsistent performance or inaccurate blood gas measurements, though the exact risk is not specified in the recall notice.
Healthcare professionals using these tubes for blood gas analysis are likely affected. Patients receiving blood tests using these tubes may be at risk if the tubes cause inaccurate results.
Check for the model number 06 0186 on the tube. Affected lots were produced from July 31, 2023, to February 28, 2025, with specific lot numbers listed in the recall notice.
Look for the model number 06 0186 on the tube and verify the production lot date against the affected dates.
The recall states the tubes were manufactured using unvalidated processes, which could lead to quality issues, but the exact risk is not specified.
The recall notice does not specify any remedy or action steps.
Lots produced from July 31, 2023, to February 28, 2025, with specific lot numbers: 23H4108, 23H4155, 23I4014, 23I4062, 23J4040, 24F4188, 24I4314, 24L4002, 25B4097.
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-0557-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0557-2026 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.
