Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection devices due to inadequate quality control during manufacturing. Products with model 07 7340 and lots from August 2023 to February 2025 are affected. No specific action is required but products should be checked for proper use.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners recalls SAFE-T-FILL Micro Capillary Blood Collection devices (model 07 7340) made between August 2023 and February 2025 because of poor manufacturing quality control. This could lead to improper blood collection if used without following safety guidelines.
The devices were made using unvalidated manufacturing processes, which could result in improper blood collection. This might cause inaccurate test results or minor issues during use, but serious injury is not expected.
People who use SAFE-T-FILL Micro Capillary Blood Collection devices for blood testing or medical procedures. Those with the model number 07 7340 and lots produced from August 2023 to February 2025 are most at risk.
Check for the model number 07 7340 on the device and the lot number (24B4201 or 24K4372) on the packaging. Products were made between August 2023 and February 2025.
Look for the model number 07 7340 on the device or packaging.
Confirm the lot number is 24B4201 or 24K4372 for products made between August 2023 and February 2025.
The recall does not require immediate action, but you should check the model and lot number to ensure you have the affected product.
The risk is low; the product may not function properly due to manufacturing issues, but serious injury is not expected.
Products were made from August 2023 to 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-0553-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0553-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
