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ASP Global, LLC. Recalls
25 recalls on record · November 5, 2025 to November 26, 2025 · Medical Devices
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Collection Tube Extender, Model 09 1004
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls Mixing Fleas for SAFE-T-FILL Blood Gas Capillaries, Model 07 9503
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Magnetic Rings for SAFE-T-FILL Blood Gas Capillaries, Model 07 9502
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL End Caps for SAFE-T-FILL Blood Gas Capillaries; Fits outer diameter 1.6 - 2.1mm, Model 06 0402 Product D
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 115 ¿L; Prepared with Balanced Heparin Model/Catalog Number: 06 0185
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L; Prepared with Sodium Heparin Model/Catalog Number: 06 0009 P
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Prepared with Sodium Heparin Model/Catalog Number: 06 0007 Pr
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 115 ¿L; Prepared with Sodium Heparin Model/Catalog Number: 06 0005 P
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Untreated. Model 06 0199 Product Description: A clear,
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L; Prepared with Balanced Heparin, Model/Catalog Number: 06 0187
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Prepared with Balanced Heparin Model 06 0186 Product Descr
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL MicroHematocrit Capillary Tubes, 50 ¿L; Untreated, Blue Markings Model/Catalog Number: 06 0508 Product
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL MicroHematocrit Capillary Tubes, 50 ¿L; Plastic, Ammonium Heparinized, Red Marking Model/Catalog Number: 06
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator; Amber Microtube, Red Model/Catalog
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Sodium Fluoride; Gray Model/Catalog Number: 07 7340
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Lithium Heparin; Green Model/Catalog Number: 07 725
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Lithium Heparin; Green Model/Catalog Number: 07 725
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Lithium Heparin and Plasma Separator Gel; Green Mod
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls AFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Lithium Heparin and Plasma Separator Gel; Green Mode
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Clot Activator; Red Model/Catalog Number: 07 7151
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator; Red Model/Catalog Number: 07 7150
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Clot Activator and Serum Separator Gel; Red Model/C
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator and Serum Separator Gel; Red Model/C
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 26, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L; Prepared with Lithium Heparin; Green Model/Catalog Number: 07 610
Hazard: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
November 5, 2025Medical DevicesFDA
ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L Prepared with Dipotassium EDTA Purple, Model: 07 6011; SAFE-T-FILL
Hazard: 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.