Asp Global recalls

Asp Global appears in 89 official U.S. recall notices indexed by RecallRadar.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 18" X 4" 2-Line, Red Model/Catalog Number: ASP-564007 Software Version: Not…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 26" DUAL BLADDER, 2 LINE (10) Model/Catalog Number: DB-7024-02Q Software Version: N…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 12" X 3.5" 2-LINE (CS 10) PLUM Model/Catalog Number: 564003 Software Vers…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 8" X 2.5" 2-LINE (CS 10) Model/Catalog Number: 564001 Software Version: N…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 24" X 4" 1-Line, Yellow Model/Catalog Number: ASP-564008 Software Version:…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 1-LINE (CS 10) WHITE Model/Catalog Number: 564010 Software Versi…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 24" 2 LINE (10) Model/Catalog Number: DT-7024-02Q Software Version: Not Applicable…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 44" X 4" 1-Line, Green Model/Catalog Number: ASP-564014 Software Version: N…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 10) WHITE Model/Catalog Number: 564011 Software Versi…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 18" X 4" 2-LINE (CS 10) RED Model/Catalog Number: 564007 Software Version…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 44" X 4" 2-Line, Green Model/Catalog Number: ASP-564015 Software Version: N…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30" 2 LINE (10) Model/Catalog Number: DT-7030-02Q Software Version: Not Applicable…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 12" X 3.5" 2-LINE (CS 12) PLUM Model/Catalog Number: A70107003 Software V…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 1 LINE (10) Model/Catalog Number: DT-7044-01Q Software Version: Not Applicable…
  FDA Device · Class II · 2026-10-07 · Asp Global
  Reason: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
• SAFE-T-FILL MicroHematocrit Capillary Tubes, 50 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL End Caps for SAFE-T-FILL Blood Gas Capillaries
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• Mixing Fleas for SAFE-T-FILL Blood Gas Capillaries, Model 07 9503
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 115 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 115 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL MicroHematocrit Capillary Tubes, 50 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Collection Tube Extender, Model 09 1004
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Magnetic Rings for SAFE-T-FILL Blood Gas Capillaries, Model 07 9502
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• AFE-T-FILL Micro Capillary Blood Collection, 200 ¿L
  FDA Device · Class II · 2025-11-26 · Asp Global
  Reason: Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
• SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L Prepared with Dipotassium EDTA Purple, Model: 07 6011
  FDA Device · Class II · 2025-11-05 · Asp Global
  Reason: 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 positiv…