Anatomy Supply Partners recalls SAFE-T-FILL MicroHematocrit Capillary Tubes (Model 06) due to inadequate quality control during manufacturing. Affected units were produced from July 31, 2023, to February 28, 2025. No specific action is required but check for the model number.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Anatomy Supply Partners is recalling SAFE-T-FILL MicroHematocrit Capillary Tubes (Model 06) because they were made using unvalidated manufacturing processes. This could lead to inconsistent quality in the tubes, but the recall does not require immediate action.
The tubes were produced under an inadequate quality system, meaning the manufacturing processes weren't properly validated. This could result in inconsistent tube quality, but it does not pose a direct risk of injury or malfunction during normal use.
Lab technicians and medical professionals who use these tubes for blood tests may be affected. The risk is low as the issue relates to manufacturing quality, not immediate safety hazards.
Check for the model number 06 on the tube packaging. Products were manufactured from July 31, 2023, to February 28, 2025, and sold with the catalog number 06 0507.
Look for the model number 06 on the tube packaging to confirm if it's affected.
No, the recall does not require immediate action. The issue is related to manufacturing quality, not immediate safety hazards.
No specific action is required. Check the model number to confirm if it's affected, but there's no need to discard or return them.
The affected tubes were manufactured from July 31, 2023, to February 28, 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-0555-2026 — Anatomy Supply Partners Anatomy Supply Partners Hello, I own a Anatomy Supply Partners that is covered by recall Z-0555-2026 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.
