The Recall Desk

Hazard

Fluid Leak recalls

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

What the numbers show

Total
97
Critical
0
Severe
35
Most recent
2026-07-29

Of the 97 fluid 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 35 (36%) 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 fluid 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.

26–50 of 97

  • HighFDA (Devices)·Z-1374-2022·2022-07-20

    Ventana HE 600 Automated Slide Preparer Recalled for Potential Electrical Fire Risk

    Ventana Medical Systems is recalling 763 Ventana HE 600 automated slide preparer instruments used in laboratories worldwide due to potential fluid leaks that could cause electrical shorts and fire.

    Product
    Ventana HE 600 System, automated slide preparer, for use in laboratories.
    Category
    Medical Device
    Distribution
    40 states
  • SevereFDA (Devices)·Z-1316-2022·2022-07-13

    Palindrome Chronic Catheter recalled due to potential hub leakage

    Covidien is recalling Palindrome Chronic Catheters due to a potential leaking condition in the hub that may cause unexpected fluid return during use.

    Product
    Palindrome Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1317-2022·2022-07-13

    Palindrome H Chronic Catheters Recalled for Potential Hub Leaking

    Palindrome H Chronic Catheters are being recalled due to a potential leaking condition in the catheter hub that may result in unanticipated fluid return during hemodialysis treatment. Affected units have been distributed worldwide.

    Product
    Palindrome H Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1315-2022·2022-07-13

    Palindrome Precision Chronic Dialysis Catheters Risk Fluid Leakage Due to Hub Defect

    Covidien recalls 25,765 Palindrome Precision HSI Chronic Catheters due to a defect in the hub that may cause unintended fluid leakage during dialysis treatment.

    Product
    Palindrome Precision HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V660000·2021-08-25

    Thomas Built Buses Saf-T-Liner HDX Recalled for Power Steering Hose Fire Risk

    Daimler Trucks North America is recalling 2016-2021 Thomas Built Buses Saf-T-Liner HDX transit buses because the power steering hose may be routed with inadequate clearance, potentially causing damage and increasing fire risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1476-2021·2021-04-28

    Smiths Medical Recalls Manifold Rotators Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific lots of manifold rotators and related components because they may have insufficient or incomplete welds.

    Product
    Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR, OFF HANDLE, Model Number MX1232MR b. 250 3 GANG MANIFOLD ROTATOR, OFF HANDLE, Model Number MX1233MR c. 550 2 GANG MANIFOLD ROTATOR, OPEN HANDLE, Model Number MX1322MR d. 550 3 GANG MANIFOLD ROTATOR, OFF HANDLE, Mod
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V067000·2021-02-11

    Freightliner M2 Recall: Transmission Oil Cooler Line Clip May Fail

    Daimler Trucks is recalling 2014-2019 Freightliner Business Class M2 vehicles because a retaining clip may fail, causing a transmission fluid leak that increases crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V663000·2020-10-28

    Daimler Recalls 2015-2020 Sprinter Vans for Steering Hose Defect

    Daimler Vans USA is recalling 2015-2020 Mercedes-Benz and Freightliner Sprinter vans because hydraulic power steering hoses may detach, causing fluid leaks and loss of steering assist.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 1500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0266-2021·2020-10-28

    ICU Medical Recalls NanoClave Administration Sets Due to Seal Defect

    ICU Medical is recalling specific lots of NanoClave administration sets because a manufacturing defect may prevent the spike from sealing properly.

    Product
    8 IN(20cm) APPX 0.46ml, MicroClave CLEAR, NanoClave T-CONN, FILTER. 1 unit per pouch, 50 pouches per case. UDI: (01)10840619066052(17)250201(30)50(10)4717491. Administration sets and their accessories are single use, pre-sterilized devices that provide access for the administ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V568000·2020-09-21

    Nova Bus Recalls LFS Models Due to Power Steering Pipe Separation Risk

    Nova Bus is recalling 2019-2021 LFS and LFS ARTIC transit buses because power steering pipes may separate, causing fluid leaks and loss of steering assist.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V272000·2020-05-13

    Audi Recalls 2020 Q8 Models for Transmission Fluid Leak Risk

    Volkswagen is recalling 2020 Audi Q8 vehicles because a defective transmission oil pipe may leak fluid, making roads slippery and increasing crash risk.

    Product
    AUDI — AUDI Q8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V271000·2020-05-13

    Porsche Recalls 2020 Cayenne for Transmission Oil Pipe Weld Defect

    Porsche is recalling 2020 Cayenne vehicles because an insufficient weld on a transmission oil pipe may cause fluid leaks, potentially making roads slippery and increasing crash risk.

    Product
    PORSCHE — PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1778-2020·2020-04-29

    Medivators Recalls Endo SmartCap Tubing Due to Manufacturing Anomaly

    Medivators is recalling Endo SmartCap Tubing because a manufacturing anomaly may cause inadequate insufflation, air bubbles, or water leaks during endoscopic procedures.

    Product
    Medivators Endo carry-on Procedure Kit REF CPK-100222-0002 - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1776-2020·2020-04-29

    Medivators Recalls Endo SmartCap Tubing Due to Manufacturing Anomaly

    Medivators is recalling Endo SmartCap Tubing kits due to a manufacturing anomaly that may cause inadequate insufflation or water leaks during endoscopic procedures.

    Product
    Medivators EndoGator REF 100650. Kit for Olympus 140/160/180/190 Series GI Endoscopes forCO2 Connection with Olympus OFP or Boston Scientific Endostat II Irrigation Pump Units. Contents 10. Sterile EO. of 100145CO2EXT Endo SmartCap Irrigation Tubing for Olympus 140/240, 160/2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1773-2020·2020-04-29

    Medivators Recalls Endo Smartcap Endoscope Tubing Due to Manufacturing Anomaly

    Medivators is recalling Endo Smartcap Endoscope Tubing due to a manufacturing anomaly that may cause inadequate insufflation, air bubbles, or water leaks during endoscopic procedures.

    Product
    Medivators Endo Smartcap Endoscope Tubing. REF100145CO2, packaged as Contents 1, 10, 50 and found in BMP-C145CO2. Tubing for Olympus 140/240, 160/260, 180/280, 190/290 Series Endoscopes. Sterile EO - Product Usage: is intended to be used with an air or CO2 source and/or a pu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1777-2020·2020-04-29

    Medivators Recalls Endo SmartCap Tubing Due to Manufacturing Anomaly

    Medivators is recalling Endo SmartCap Tubing kits due to a manufacturing anomaly that may cause inadequate insufflation, air bubbles, or water leaks during endoscopic procedures.

    Product
    Medivators EndoGator REF 100651. Kit for Olympus 140/160/180/190 Series GI Endoscopes for CO2 Connection with Endogator EGP-100, Olympus OFP, Olympus AFU-100 & Erbe EIP 2 Irrigation Pump Units. Contents 10. Sterile EO. of 100145CO2EXT Endo SmartCap Irrigation Tubing for Ol
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1356-2020·2020-03-04

    Zimmer Sterile Disposable Tourniquet Cuff Recalled for Bladder Leak

    Zimmer Surgical Inc is recalling 58 units of sterile tourniquet cuffs because a leak between bladders may cause both to inflate or deflate simultaneously.

    Product
    Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No. 60708015200, UDI (01)00889024377547 (17)230812(10)27968701 The product is a tourniquet - Product Usage: Tourniquets are intended to be used by qualified medical prof
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0789-2019·2019-02-06

    Abbott Recalls Alinity i Processing Modules Due to Gear Pump Assembly Issue

    Abbott is recalling Alinity i Processing Modules because a gear pump assembly issue causes foaming and dried residue in the wash buffer reservoir.

    Product
    Alinity i Processing Module, (a) Part Number 03R65-01 (b) Part Number A-30108552-01 (c) Part Number A-30109694-01 Product Usage: The Alinity i processing module is a fully automated immunoassay analyzer allowing random and continuous access, as well as priority and auto
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·18V639000·2018-09-17

    Audi Recalls 2017-2018 R8 Vehicles Due to Transmission Fluid Leak Fire Risk

    Volkswagen Group of America is recalling 2017-2018 Audi R8 Spyder and Coupe vehicles because transmission fluid may leak from the gearbox ventilation hose, creating a fire risk if it contacts hot engine parts.

    Product
    AUDI — AUDI R8 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V179000·2018-03-19

    Forest River Recalls Motorhomes Due to Power Steering Hose Fire Risk

    Forest River is recalling specific 2012-2017 motorhomes because an incorrectly routed power steering hose may rub against the starter motor, causing electrical arcing and a fire risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN, GLAVAL BUS CHARLESTON, BERKSHIRE, PATHFINDER, CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0090-2018·2017-11-22

    WalkMed Infusion Pump Reservoir Bags Recalled for Fluid Leaks

    WalkMed, LLC is recalling 25,920 infusion pump reservoir bags due to reported fluid leaks at the luer connection.

    Product
    Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Number IPR-86/10 65 mL and Reservoir Bag for WalkMed Infusion Pump Part Number 204821 Catalog Number IPR-150/10 150 mL The WalkMed Reservoir Bag is designed for use with the WalkMed 350VL Ambulatory pump and is i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2755-2017·2017-08-02

    Medtronic Visualase Cooled Laser Applicator System Recalled for Seal Defect

    Medtronic is recalling 214 units of the Visualase Cooled Laser Applicator System because the cap may fail to seal, causing saline leaks.

    Product
    Medtronic Visualase(R) Cooled Laser Applicator System (VCLAS) 15MM TIP, REF 9735561, (1) Laser Diffusing Fiber - 600um Core, 15mm Tip, (1) Cooling Catheter with 3M(TM) SteriStrip(TM), (1) Pump Tubing Set, (1) Drainage Bag. Medtronic Navigation, Inc. Louisville, CO 80027
    Category
    Medical Device
    Distribution
    7 states
  • SevereNHTSA·17V390000·2017-06-21

    Aston Martin Recalls 2012 V8 Vantage for Transmission Fluid Leak Risk

    Aston Martin is recalling 2012 V8 Vantage vehicles because a transmission connector may break, causing a fluid leak that could prevent shifting or cause the vehicle to roll away.

    Product
    ASTON MARTIN — ASTON MARTIN V8 VANTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V391000·2017-06-21

    Aston Martin Recalls V8 Vantage for Transmission Fluid Leak Risk

    Aston Martin is recalling 2011-2014 V8 Vantage vehicles because a broken clutch fluid line connector may cause hydraulic leaks, preventing gear shifting or causing the vehicle to roll away.

    Product
    ASTON MARTIN — ASTON MARTIN V8 VANTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide