Hazard

Bleeding recalls

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

What the numbers show

Total: 177
Critical: 11
Severe: 84
Most recent: 2026-09-02

Of the 177 bleeding recalls we have scored against our rubric, 11 (6%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 84 (47%) 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 bleeding 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.

51–75 of 177

HighFDA (Devices)·Z-1859-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Line Holes
Maquet Cardiovascular is recalling specific Hemashield Gold vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M002020955010 - Product Usage: For use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1870-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Defects
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175824P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1877-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at the seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175914P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1881-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Defects
Maquet is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175928P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1880-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175926P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1866-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Bleeding Risk
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175732P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1878-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Potential Seam Holes
Maquet is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175922P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1874-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175832P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1879-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Bleeding Risk
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175924P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1873-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Defects
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175830P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1862-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal, Product Code: M00202175426T0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1796-2020·2020-05-06
Merit Medical Recalls PreludeSYNC Radial Compression Devices Due to Balloon Defects
Merit Medical Systems is recalling PreludeSYNC Radial Compression Devices because inflatable balloons may break, causing air leakage and potential bleeding.
Product
PreludeSYNC DISTAL Radial Compression Devices, SDRB-REG-LT, SDRB-REG-RT
Category
Medical Device
Distribution
33 states
SevereFDA (Devices)·Z-1889-2019·2019-07-03
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer Recalled for Bleeding Risk
Ethicon is recalling ENSEAL X1 Curved Jaw Tissue Sealers due to a reported incidence of intraoperative bleeding.
Product
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 37cm Shaft PRODUCT CODE: NSLX137C
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1888-2019·2019-07-03
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer Recalled for Bleeding Risk
Ethicon Endo-Surgery Inc is recalling ENSEAL X1 Curved Jaw Tissue Sealers due to reported intraoperative bleeding.
Product
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1890-2019·2019-07-03
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer Recalled for Bleeding Risk
Ethicon Endo-Surgery Inc is recalling ENSEAL X1 Curved Jaw Tissue Sealers due to reported intraoperative bleeding.
Product
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 45cm Shaft PRODUCT CODE: NSLX145C
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1832-2019·2019-06-26
Recall of Signia Tri-Staple 2.0 Surgical Reloads Due to Missing Pins
Covidien LLC is recalling Signia Tri-Staple 2.0 reloads because missing pin components may cause incomplete staple formation, potentially leading to serious surgical complications.
Product
SIGNIA TRI-STAPLE 2.0 30MM MEDIUM/ THICK RELOAD , SIG30AMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1835-2019·2019-06-26
Recall of Signia Tri-Staple Surgical Devices Due to Missing Pin Components
Covidien LLC is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, potentially leading to serious surgical complications.
Product
SIGNIA TRI-STAPLE 2.0 CURVED TIP 45MM MEDIUM/ THIC , SIG45CTAMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1826-2019·2019-06-26
Covidien EGIA 45 Articulating Medical Stapler Recall for Missing Pins
FDA is recalling 3.1 million EGIA 45 staplers due to missing pins that may cause incomplete stapling and serious surgical complications.
Product
EGIA 45 ARTICULATING MED THICK SULU, Item Code EGIA45AMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1833-2019·2019-06-26
Recall of Signia Tri-Staple 2.0 Reloads Due to Missing Pin Components
Covidien LLC is recalling Signia Tri-Staple 2.0 reloads because missing pin components may cause incomplete staple formation, leading to serious surgical complications.
Product
SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA, SIG45AXT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1830-2019·2019-06-26
Covidien EGIA 60 Curved Tip Surgical Stapler Recall for Missing Pins
FDA is recalling 3,113,280 units of the EGIA 60 Curved Tip Art Med Thick Sulu surgical stapler because missing pin components may cause incomplete staple formation and serious medical complications.
Product
EGIA 60 CURVED TIP ART MED THICK SULU, EGIA60CTAMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1829-2019·2019-06-26
Covidien EGIA 60 Articulating Medical Stapler Recall for Missing Pins
FDA is recalling 3,113,280 units of the EGIA 60 Articulating Medical Stapler due to missing pin components that may cause incomplete staple formation and serious surgical complications.
Product
EGIA 60 ARTICULATING MED THICK SULU , EGIA60AMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1828-2019·2019-06-26
FDA Recalls Covidien EGIA 60 Articulating Extra Thick Sulu Devices
The FDA is recalling 3,113,280 units of the EGIA 60 Articulating Extra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious surgical complications.
Product
EGIA 60 ARTICULATING EXTRA THICK SULU, Item code EGIA60AXT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1827-2019·2019-06-26
FDA Recalls 3.1 Million Covidien EGIA 45 Articulating Xtra Thick Sulu Devices
The FDA is recalling 3,113,280 units of the EGIA 45 Articulating Xtra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious medical complications.
Product
EGIA 45 ARTICULATING XTRA THICK SULU, Item Code EGIA45AXT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1825-2019·2019-06-26
FDA Recalls Covidien EGIA 30 Articulating Medical Devices
The FDA is recalling 3,113,280 units of the EGIA 30 Articulating Medical device due to missing pin components that may cause incomplete staple formation and serious surgical complications.
Product
EGIA 30 ARTICULATING MED THICK SULU, Item Code EGIA30AMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1834-2019·2019-06-26
FDA Recalls Signia Tri-Staple 2.0 Devices Due to Missing Pin Components
The FDA is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, leading to serious surgical complications.
Product
SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA, SIG60AXT
Category
Medical Device
Distribution
Distributed nationwide