Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection tubes due to inadequate quality control during manufacturing. Affected lots produced from August 2023 to February 2025 may have unvalidated processes.
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 tubes that were made with unvalidated manufacturing processes. This could lead to quality issues with the blood collection tubes, though serious injury risks are not specified in the recall.
The tubes were manufactured using unvalidated processes that may not meet quality standards. This could result in improper blood collection or inaccurate test results, but the recall does not mention risks of injury or serious harm.
People who use these blood collection tubes for finger or heelstick blood draws may be affected. Healthcare providers and individuals performing home blood tests are most at risk.
Check for the model number 07 7121 on the tube packaging. The affected lots were produced from August 2023 through February 2025 with specific batch codes.
Look for the model number 07 7121 and batch codes 23J4038, 24B4194, 24B4195, 24D4020, 24H4128, or 24J4337 on the tube packaging.
The product was manufactured using unvalidated processes that may not meet quality standards.
Check the model number and batch codes to see if your product is affected. If it is, contact Anatomy Supply Partners for guidance.
The recall does not mention risks of injury or serious harm, so the risk level is low.
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-0546-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0546-2026 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.
