ASP Global, LLC. dba Anatomy Supply Partners, LLC.

25 FDA enforcement actions

25 Total Recalls

0 Class I

25 Class II

0 Class III

Firm Details

Product Types: device
States: GA

All Recalls

Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 09/26/2025 device

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Class II: Risk 05/05/2025 device

All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured between July 31, 2023 to February 28, 2025 cause false positive results when used with Magellan Diagnostics LeadCare Testing Systems. False positive lead results may cause delayed results and additional unnecessary testing.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.