RegWardenFDA facility compliance records
Recall

Class II — ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalling firmASP Global, LLC
Registered facilityASP Global, LLC (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonDue to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
ProductAFE-T-FILL Micro Capillary Blood Collection, 200 L; Prepared with Lithium Heparin and Plasma Separator Gel; Green Model/Catalog Number: 07 7220 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.
Quantity49000
DistributionDistribution US nationwide and Canada.
Initiated2025-09-26
Classified2025-11-19
Recall numberZ-0549-2026
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — ASP Global, LLC. dba Anatomy Supply Partners, LLC. (Z-0549-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97592/

Not open yet

Alerts for ASP Global, LLC

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.