Hazard

Occlusion recalls

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

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all occlusion 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.

126–142 of 142

HighFDA (Devices)·Z-0361-2023·2022-12-14
Dover Urinary Catheter Drainage Bag Port Occlusion Recall
Cardinal Health is recalling Dover closed urethral catheter trays due to potential occlusion of the drainage bag inlet port, which may prevent proper urine drainage and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 1000 mL Drainage Bag Product Code: 3450LF Intended for urinary drainage from the bladder of a patient.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1077-2022·2022-05-25
FDA Recalls iCast Covered Stent System Due to Device Separation During Delivery
Atrium Medical is recalling the iCast Covered Stent System because the balloon or catheter hub may separate from the delivery catheter during use, potentially causing blood clots, vessel blockages, or organ damage.
Product
iCast Covered Stent System Product Code/Part Number: 85400 85401 85402 85403 85404 85405 85406 85407 85408 85409 85410 85411 85412 85413 85414 85415 85416 85417 85418 85419 85420 85424 85440 85441 85442 85443 85444 85445 85450 85451 85452 85453
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2466-2021·2021-09-22
BD Alaris Infusion Pump Buerette Set Connector Valve Occlusion Issues
BD Alaris needle-free connector valves in Buerette Sets may develop occlusions, difficulty flushing, or flow issues that could delay patient therapy. The product was distributed worldwide across all US states and multiple countries.
Product
BD Alaris Pump Infusion Buerette Set Smallbore Tubing Smartsite Port (Burette) 3 SmartSite Y-Sites, REF: 2441-0006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2464-2021·2021-09-22
Needle-Free Burette Set Valves Recalled for Occlusion and Flow Issues
BD ADD-ON Burette Set V/NV Needle-Free Valves may experience occlusions or flow issues that could delay therapy. CAREFUSION recalled 44,120 units with this defect.
Product
BD ADD-ON Burette Set V/NV Needle-Free Valve, REF: 82113E-0006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2463-2021·2021-09-22
BD Gravity IV needle-free connector valve occlusion risk
BD Gravity IV needle-free connector valves may develop flow issues and partial or total occlusions that could delay therapy. The recall affects 24,360 units distributed worldwide.
Product
BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free Y-sites, REF: CM42500E-07; BD Gravity IV Set 3-port Closed Stopock Manifold Back Check Valve 2 Needle-Free Y-sites, REF: CS42522E-07; BD GRAVITY 10 DP V/NV CHECK VALVE 3-WAY STOPCOCK 4 Smartsite VALVES & Smar
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2460-2021·2021-09-22
BD needle-free connector valves recalled for flow obstruction risk
BD needle-free connector valves and extension sets may experience flow obstruction and flushing difficulties, potentially delaying medical therapy. No adverse events have been reported.
Product
BD Extension Set SMALLBORE Tubing SmartSite VALVE, REF: 10010511; BD SmartSite Extension Set Needle-Free Valve, REF: 10010912; BD EXTENSION SET SMALLBORE TUBING DETACHABLE SmartSite VALVE, REF: 10010983; BD Gravity Burette Set 60 DP 4 VersaSafe PORTS 3 SmartSite VALVES BALL VALV
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2461-2021·2021-09-22
BD SmartSite Bag Access Device Recalled for Valve Occlusion Issues
CAREFUSION is recalling BD SmartSite Bag Access Device needle-free connector valves due to potential occlusions and flow issues that could delay therapy delivery.
Product
BD SmartSite Bag Access Device, REF: 2300E-0500; BD BAG ACCESS DEVICE CHECK VALVE SmartSite VALVE, REF: 2309E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2465-2021·2021-09-22
BD SE Burette Set needle-free connectors recalled for flow obstruction risk
CareFusion is recalling BD SE Burette Sets with needle-free connector valves that may fail to flush or develop flow obstructions, risking therapy delays. Approximately 56,680 units were distributed worldwide.
Product
BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2455-2021·2021-09-22
BD SmartSite Needle-Free Valve Extension Set Recalled for Potential Occlusion
CareFusion recalls BD SmartSite needle-free valve extension sets due to potential occlusion, flow issues, and difficulty flushing that could delay medical therapy.
Product
BD SmartSite 'Y' Extension Set 2 Needle-Free Valves, REF: 20019E7D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2459-2021·2021-09-22
BD Alaris Infusion Pump Buerette Sets Needle-Free Connector Valve Issues
BD Alaris Pump Infusion Buerette Sets with needle-free connector valves may experience flushing difficulties, flow issues, or occlusions that could delay therapy delivery. No illnesses or injuries have been reported.
Product
BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Tubing SmartSite Port (Burette) SmartSite Y-Site, REF: 10015012; BD Alaris Pump Infusion Buerette Set Ball Valve Smallbore Tubing Smartsite Port (Burette) SmartSite Y-Site, REF: 10817920; BD Alaris Pump Infusion Bue
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2468-2021·2021-09-22
BD Needle-Free Bag Access Valves Recalled for Flow Obstruction
BD SmartSite needle-free valves may become obstructed, preventing proper fluid flow in medical infusions. The FDA recalls over 295,000 units due to risk of therapy delays.
Product
BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E; BD Bag access Device with 1 Check Valve And Needle Free Valve, REF: 2309E-0006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2456-2021·2021-09-22
FDA recalls BD burette sets for connector valve occlusion and flow defects
BD Gravity Burette Sets and Add-On Burette Sets are being recalled due to needle-free connector valve defects that may cause flushing difficulties, flow problems, or complete occlusions, potentially delaying therapy. The recall affects approximately 77,802 units distributed worldwide.
Product
BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV, REF: 10037031; BD Gravity Burette Set 20 DROP 1.2 Micron Filter 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV , REF: 10037032; BD GRAVITY BURETTE SET 60 DROP 2 Smartsite VALVES BALL DRIP CHAM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2454-2021·2021-09-22
Extension Set SMALLBORE Tubing with SmartSite Valves Recalled for Flushing Issues
BD Extension Set SMALLBORE Tubing with SmartSite Valves (REF: 20019E) is being recalled due to flushing difficulties, flow issues, and occlusions that could delay therapy. Over 1.4 million units distributed worldwide are affected.
Product
BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2467-2021·2021-09-22
BD SmartSite Needle-Free Connector Valves Recalled for Flow and Occlusion Issues
CAREFUSION is recalling BD SmartSite needle-free connector valves due to difficulty flushing, flow issues, and occlusions that could delay therapy. Approximately 23.8 million units were distributed worldwide.
Product
BD SmartSite, REF: 2000E CHINA; BD SmartSite Connector, REF: 2000E-04; BD SmartSite J-LOOP Extension Set One Needle Free Valve, REF: 20021E7D; BD SmartSite Extension Set One Needle Free Valve Slip Luer, REF: 20037E7D; BD SmartSite Extension Set 3 Needle Free Valves, REF: 20038E7D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2458-2021·2021-09-22
BD needle-free connector valves may occlude or restrict fluid flow
BD Burette Gravity Set needle-free connector valves may fail to flush or develop blockages, potentially delaying patient therapy. Lot 21015553 consists of approximately 630 units distributed worldwide.
Product
BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED, REF: 42163E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1839-2021·2021-06-16
Medical Device Illumination Pack Recalled Due to Burn and Occlusion Risks
Nico Corp. is recalling 439 NICO Myriad-LX Illumination Packs used in surgical procedures due to potential delivery sleeve occlusion and thermal burn injury from the fiber tip assembly.
Product
NICO Myriad-LX Illumination Pack: REF: NN-1000 Mvriad-LX Illumination Pack. 11ga REF: NN-1001 Mvriad-LX Illumination Pack. l3ga Intended to perform resection and removal of soft tissues and fluids under direct visualization accessories to the NICO Myriad System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1840-2021·2021-06-16
Myriad-LX Light Source Recalled Due to Burn and Occlusion Risk
Nico Corp. is recalling 80 Myriad-LX Light Source units due to potential burn injury to patients from the distal tip of the fiber assembly and risk of delivery sleeve occlusion during surgical use.
Product
Myriad-LX Light Source-for delivery of light to the surgical field to enhance visualization of tissue during resection Part Number NN-7013 The Myriad-LX light source is a high-intensity 300W Xenon illuminator with a touch screen and digital dimming controls. The source is fit
Category
Medical Device
Distribution
Distributed nationwide