Hazard

Blood Loss recalls

61 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 61
Critical: 1
Severe: 26
Most recent: 2026-08-05

Of the 61 blood loss recalls we have scored against our rubric, 1 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 26 (43%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all blood loss recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

51–61 of 61

HighFDA (Devices)·Z-1387-2017·2017-03-08
Cook Inc. Recalls Check-Flo Performer Introducers Due to Blood Loss Reports
Cook Inc. is recalling 884 Check-Flo Performer Introducers because a specific valve design is associated with increased reports of blood loss.
Product
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices.
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1389-2017·2017-03-08
Cook Inc. Recalls Check-Flo Hemostasis Assemblies Due to Blood Loss Reports
Cook Inc. is recalling 1,589 Check-Flo Hemostasis Assemblies because reports indicate increased blood loss associated with the device's valve design.
Product
Check-Flo Hemostasis Assembly, Individual product is packaged in a Tyvek-film sterilizable outer pouch.
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1391-2017·2017-03-08
Cook Inc. Recalls Micropuncture Check-Flo Performer Introducer Sets Due to Blood Loss
Cook Inc. is recalling 778 Micropuncture Check-Flo Performer Introducer Sets because a specific valve design is associated with increased reports of blood loss.
Product
Micropuncture Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1393-2017·2017-03-08
Cook Inc. Recalls TriForce Peripheral Crossing Sets Due to Blood Loss Reports
Cook Inc. is recalling 1,875 TriForce Peripheral Crossing Sets because a specific valve design is associated with increased reports of blood loss.
Product
TriForce Peripheral Crossing Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The TriForce Peripheral Crossing Set is intended to be percutaneously introduced into blood vessels and support a wire guide while performing percutaneous peripheral interv
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1392-2017·2017-03-08
Cook Inc. Recalls Check-Flo Introducer Devices Due to Blood Loss Reports
Cook Inc. is recalling 29 Check-Flo Introducer Hausdorf-Lock Atrial devices worldwide due to increased reports of blood loss associated with the hemostatic valve design.
Product
Check-Flo Introducer Hausdorf-Lock Atrial, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-2738-2016·2016-09-14
Terumo Recalls Pinnacle Introducer Sheaths Due to Valve Leakage
Terumo Medical Corporation is recalling Pinnacle Introducer Sheaths due to a manufacturing issue causing valve leakage, which poses a risk of incremental blood loss.
Product
PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath PINNACLE¿ TIF TIP" Introducer Sheath PINNACLE¿ R/O II Radiopaque Marker Introducer Sheath
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1828-2015·2015-07-01
Terumo Recalls Custom Cardiovascular Procedure Kits and Safety Valves
Terumo is recalling 163 custom cardiovascular procedure kits and over-pressure safety valves because the valves are not cleared for use on the arterial side of the bypass circuit.
Product
Custom Cardiovascular Procedure Kits; Over-Pressure Safety Valves. For use only in the extracorporeal circuit for the cardiopulmonary bypass procedures for which the user designed it.
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-1456-2015·2015-04-29
OriGen VV13F Reinforced Dual Lumen Catheter Recalled for Separation Risk
OriGen Biomedical is recalling 51 units of VV13F Reinforced Dual Lumen Catheters because the extension tube may separate from the hub, posing a risk of blood loss.
Product
OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter STERILE DISPOSABLE: DO NOT RE-USE Manufactured by: OriGen Biomedical. OriGene VV13F Reinforced Dual Lumen Catheter indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0186-2014·2013-11-20
Fresenius Medical Care Recalls Combiset Blood Lines for Hemodialysis
Fresenius Medical Care is recalling 508,029 cases of Combiset Blood Lines for hemodialysis because connections may disconnect if not tightened correctly, leading to blood loss.
Product
Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0184-2014·2013-11-20
Fresenius Hemodialysis Blood Lines Recalled for Potential Disconnection Risk
Fresenius Medical Care is recalling 8,528 cases of 2008K@ Home Blood lines due to a risk of disconnection and blood loss if not tightened correctly.
Product
2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis use Catalog Number: 03-2962-3. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0185-2014·2013-11-20
Fresenius Medical Care Recalls Combiset Blood Lines for Hemodialysis
Fresenius Medical Care is recalling 24,202 cases of Combiset Blood Lines with BVM for hemodialysis. The recall addresses a risk of blood loss if connections are not tightened correctly.
Product
Combiset Blood Line with BVM for Hemodialysis use Catalog Number: 03-2965-9. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.
Category
Medical Device
Distribution
Distributed nationwide