Hazard

Air Leak recalls

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

What the numbers show

Total: 16
Critical: 0
Severe: 0
Most recent: 2024-09-25

Of the 16 air leak recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

Which agencies issued them

About this hazard tag

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

1–16 of 16

HighFDA (Devices)·Z-3180-2024·2024-09-25
Beckman Coulter Analyzer Recalled for Pneumatic Tubing Defects
Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to undersized pneumatic tubing in the reagent storage module, which can cause air leaks and compressor failures, potentially leading to test errors and delayed results.
Product
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Model Number C21510, RSM Pneumatic Tubing Kit item #2, REF C11137; in vitro diagnostic instrument
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V226000·2021-04-01
2021 International RH and LT Vehicles Parking Brake Defect
Certain 2021 International RH and LT vehicles have a defective spring brake chamber that may allow the parking brake to malfunction, increasing crash risk. Navistar will replace the defective brake chambers at no cost.
Product
INTERNATIONAL — INTERNATIONAL RH, LT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V101000·2021-02-22
2021 Mazda Mazda3 and CX-30 tire air valve failure recall
Mazda is recalling 2021 Mazda3 and CX-30 vehicles because air may leak from the tire air valve, potentially causing loss of vehicle control. Mazda will replace all tire air valves at no cost.
Product
MAZDA — MAZDA CX-30, MAZDA3
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1890-2020·2020-05-13
Intuitive Surgical Recalls daVinci XI Sureform Stapler Reloads Due to Deployment Defect
Intuitive Surgical is recalling 22,752 daVinci XI Sureform 60 reloads worldwide because a manufacturing variation may prevent adjacent staples from deploying, potentially causing an incomplete staple line.
Product
daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm, REF 48360G-08, UDI: 00886874113844, Rx Only, Sterile EO - Product Usage: are intended to be used with da Vinci Surgical Systems for resection, transection, and, or creation of anastomoses in General, Thoracic, Gynecologi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1891-2020·2020-05-13
Intuitive Surgical Recalls daVinci XI Sureform 60 Reloads Due to Staple Deployment Issues
Intuitive Surgical is recalling specific daVinci XI Sureform 60 Reloads because a manufacturing variation may prevent adjacent staples from deploying, potentially causing an incomplete staple line.
Product
daVinci XI Sureform 60 Reload, 60 mm black 6-Row 4.6 mm, Ref: 48360T-08 , UDI: 00886874113851, Rx only, SterileEO - Product Usage: are intended to be used with da Vinci Surgical Systems for resection, transection, and, or creation of anastomoses in General, Thoracic, Gynecologic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0593-2020·2019-12-11
Stryker Recalls Disposable Tourniquet Cuffs Due to Air Leak Risk
Stryker is recalling 16,380 disposable tourniquet cuffs because they may leak air, causing a loss of vascular occlusion during surgery.
Product
Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 2PRT(Dual Port) Quick Connect Connector, Product Number 5921-018-235 - Product Usage: The Stryker Disposable Tourniquet Cuff (cuff) is indicated for use in surgical procedures that require the tempora
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0592-2020·2019-12-11
Stryker Recalls Disposable Tourniquet Cuffs Due to Air Leak Risk
Stryker is recalling 16,380 disposable tourniquet cuffs because they may leak air, causing a loss of vascular occlusion during surgery.
Product
Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 1PRT(Single Port) Quick Connect Connector, Product Number 5921-018-135 - Product Usage: The Stryker Disposable Tourniquet Cuff (cuff) is indicated for use in surgical procedures that require the tempo
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V739000·2019-10-16
Hyundai Translead Recalls 2018-2019 Dry Van Trailers for Air Hose Defect
Hyundai Translead is recalling 2018-2019 Dry Van Trailers because a beam clip may detach, allowing air hoses to drag on the ground and potentially leak air.
Product
HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DRY VAN TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V513000·2016-07-07
Renegade Vienna and Villagio Recalled for Valve Stem Air Leak Risk
Kibbi is recalling 2014-2016 Renegade Vienna and Villagio vehicles because valve stem extensions may loosen, causing slow air leaks and increasing the risk of tire failure and a crash.
Product
RENEGADE — RENEGADE VILLAGIO, VIENNA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1678-2015·2015-06-03
Halyard KimVent Closed Suction System Recalled for Potential Valve Defect
Halyard Health is recalling specific KimVent Turbo-Cleaning Closed Suction Systems for adults because a defective internal valve may allow air to leak from the ventilator circuit.
Product
KimVent Turbo-Cleaning Closed Suction System for Adults, 10 F T-Piece (Product Code 227105); KimVent Turbo-Cleaning Closed Suction System for Adults, 12 F, DSE (Product Code 2271603); KimVent Turbo-Cleaning Closed Suction System for Adults, 12 F, T-Piece (Product Code 227135).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1220-2015·2015-03-11
Halyard Health Recalls KimVent Closed Suction Systems Due to Defects
Halyard Health is recalling KimVent Closed Suction Systems for Adults because a hole or crack was found that may cause air to leak.
Product
KimVent Closed Suction System for Adults, Double Swivel Elbow, 12 Fr., Sterile, Distributed by Kimberly Clark Global Systems, LLC.
Category
Medical Device
Distribution
11 states
HighFDA (Devices)·Z-1222-2015·2015-03-11
Halyard Health Recalls KimVent Wet Pak Closed Suction Systems
Halyard Health is recalling KimVent Wet Pak closed suction systems because a defect may cause air leaks.
Product
KimVent Wet Pak, Closed Suction System for Adults, Double Swivel Elbow, 14 Fr. Sterile, Distributed by Kimberly Clark Global Systems, LLC.
Category
Medical Device
Distribution
11 states
HighFDA (Devices)·Z-1221-2015·2015-03-11
Halyard Health Recalls KimVent Closed Suction Systems Due to Air Leak Defect
Halyard Health is recalling KimVent Closed Suction Systems for Adults because a hole or crack may cause air to leak. The recall affects 5 cases distributed to specific US states and Japan.
Product
KimVent Closed Suction System for Adults, Double Swivel Elbow, 14 Fr. Sterile, Distributed by Kimberly Clark Global Systems, LLC.
Category
Medical Device
Distribution
11 states
HighFDA (Devices)·Z-2038-2014·2014-07-16
Pall Medical Breathing Circuit Filter Recall for Possible Air Leak
Pall Corporation is recalling specific lots of Medical Breathing Circuit Filters due to a possible leak at the filter end cap junction.
Product
PALL Medical Breathing Circuit Filter, REF BB50T and BB50T-BULK , Rx ONLY Single use, bi-directional bacterial/viral removal filter. The filters are individually packaged in a clear, plastic pouch with black writing - 50 per case, or in bulk packaged 100 filters/bag and two
Category
Medical Device
Distribution
15 states
ModerateFDA (Devices)·Z-0113-2014·2013-11-06
Beckman Coulter LH 750 and LH 780 Hematology Analyzers Recalled for Valve Failure
Beckman Coulter is recalling LH 750 and LH 780 hematology analyzers because check valves may fail, causing air or liquid leaks.
Product
COULTER LH 750 and LH 780 Analyzers. The COULTER LH 750 Hematology Analyzer is a quantitative, automated hematology analyzer and leukocyte differential counter For In Vitro Diagnostic Use in clinical laboratories. The COULTER LH 750 Hematology Analyzer provides automated Reti
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·05511·2004-11-17
Ocean Management Systems Recalls Rotating Cross Bar SCUBA Manifolds
Ocean Management Systems is recalling about 140 Rotating Cross Bar SCUBA Manifolds because undersized o-rings can cause a loss of breathing air, presenting a risk of drowning.
Product
Rotating Cross Bar SCUBA Manifold
Category
Consumer Product
Distribution
Distributed nationwide