Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC. dba Anatomy Supply Partners, LLC. Due to Due to products manufactured under an inadequate quality...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact ASP Global, LLC. dba Anatomy Supply Partners, LLC. directly.
Affected Products
SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator and Serum Separator Gel; Red Model/Catalog Number: 07 7120 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.
Quantity: 50050
Why Was This Recalled?
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ASP Global, LLC. dba Anatomy Supply Partners, LLC.
ASP Global, LLC. dba Anatomy Supply Partners, LLC. has 25 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report