Anatomy Supply Partners recalls SAFE-T-FILL Magnetic Rings (Model 07 9502) due to inadequate quality control during manufacturing. Affected units were produced from June 2022 to February 2025. No specific action is required as the hazard is not immediately dangerous.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling SAFE-T-FILL Magnetic Rings for Blood Gas Capillaries (Model 07 9502) because they were made using unvalidated manufacturing processes. This could lead to inconsistent product quality, but the recall does not require immediate action as the hazard is not immediately dangerous.
The magnetic rings were produced under an inadequate quality system, which means the manufacturing processes were not properly validated. This could result in inconsistent product quality, but it does not pose an immediate risk of injury or malfunction during normal use.
Healthcare professionals using SAFE-T-FILL Blood Gas Capillaries with the recalled magnetic rings. The risk is minimal as the hazard is related to manufacturing quality, not immediate safety hazards.
Check for the model number 07 9502 on the magnetic rings. The affected units were produced from June 2022 to February 2025, with specific lot numbers listed in the recall notice.
Review the model number and production dates to confirm if your item is affected.
No, the recall does not require immediate action as the hazard is related to manufacturing quality, not immediate safety risks.
The recall does not specify any action steps, so no immediate action is needed.
Check for the model number 07 9502 and production dates between June 2022 and 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-0565-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0565-2026 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.
