The Recall Desk

Archive

November 2025 recalls

538 recalls were announced in November 2025.

What the numbers show

Critical
62
Severe
48
High
306
Moderate
118
Low
4

Of the 538 recalls this month scored against our rubric, 12% are Critical, 9% are Severe.

Which agencies issued them

201–300 of 538

  • HighFDA (Devices)·Z-0470-2026·2025-11-19

    Small jaw sealers recalled over residual material that may dislodge

    Medline is recalling 18,117 reprocessed LigaSure Small Jaw instruments because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal LigaSure Small Jaw Instrument (Purple/White), Compatible with FT10 Generator 18.8 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0483-2026·2025-11-19

    Fifteen millimetre snares recalled over holes compromising package sterility

    Olympus is recalling 18,174 Single Use Electrosurgical Snares SD-400U-15 because sterility may be compromised by small holes formed during packaging or transportation.

    Product
    Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Single Use Single Use Electrosurgical Snare Model/Catalog Number: SD-U400U-15 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0494-2026·2025-11-19

    Nasal feeding tubes recalled from a second lot for possible occlusion

    Applied Medical Technology is recalling NutraGlide 5 F-6 F x 55 nasal feeding tubes with stylet and ENfit, REF NFT-05055-I, from one lot because the tube may be occluded.

    Product
    Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0490-2026·2025-11-19

    Reprocessed ultrasonic shears recalled because they may stick in the on position

    Stryker Sustainability Solutions is recalling 22,476 reprocessed HARMONIC FOCUS shears because a manufacturing issue may leave them stuck in the on position, causing continuous activation.

    Product
    HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use, STERILEEO, RX ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0456-2026·2025-11-19

    Portrait vital signs monitors recalled over batteries losing backup power

    GE Healthcare is recalling 5,990 Portrait VSM patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.

    Product
    Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0481-2026·2025-11-19

    Oxygen concentrator batteries recalled over a chip that can stop oxygen

    Philips Respironics is recalling 56 SimplyGo Mini standard battery kits because a defective chip can make the battery fail, shutting down the concentrator and stopping oxygen delivery.

    Product
    SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mini Portable Oxygen Concentrator Product code: 1113600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0459-2026·2025-11-19

    Deep brain stimulators recalled over loss of programmer communication

    Abbott Medical is recalling 722 Liberta RC deep brain stimulation implantable pulse generators because the devices may lose communication with the clinician programmer or patient controller.

    Product
    Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0478-2026·2025-11-19

    Spinal fixation screws recalled for not meeting performance standards

    Orthofix is recalling 624 Virata preassembled polyaxial screws used in the Virata Spinal Fixation System because the screws do not meet performance standards.

    Product
    Virata Preassembled Polyaxial Screw, utilized in the Virata Spinal Fixation System. The following sizes are affected: 1. POLYAXIAL SCREW, CC, 5.5mm X 30mm; Item Number: TL1-10755030. 2. POLYAXIAL SCREW, CC, 5.5mm X 35mm; Item Number: TL1-10755035. 3. POLYAXIAL SCREW, CC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0172-2026·2025-11-19

    Cinnamon powder recalled over elevated levels of lead and chromium

    Singh Trading, doing business as Roshni Foods, is recalling 48 cases of Roshni Cinnamon Powder 3.5 oz because it may contain elevated levels of lead and chromium.

    Product
    Roshni Cinnamon Powder, 3.5 oz (100g). This product is packaged in clear plastic pouches.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0476-2026·2025-11-19

    Reprocessed vessel sealers recalled over residual material that may dislodge

    Medline is recalling 57,244 reprocessed LigaSure Maryland Jaw sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.

    Product
    Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated, Compatible w/FT10 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0473-2026·2025-11-19

    Blunt tip sealers recalled over residual material trapped inside the device

    Medline is recalling 60,917 reprocessed LigaSure Blunt Tip sealer/dividers, 37 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0453-2026·2025-11-19

    Patient monitors recalled over batteries that can lose backup power

    GE Healthcare is recalling 3,271 Carescape B450 patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.

    Product
    Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Record updated 3/19/26 to include: CARESCAPE B450 MBA313 2095800-001 CARESCAPE M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0472-2026·2025-11-19

    Short blunt tip sealers recalled over residual material that may dislodge

    Medline is recalling 65 reprocessed LigaSure Blunt Tip sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline RenewalLigasure Blunt Tip Sealer/Divider, NanoCoated Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0485-2026·2025-11-19

    Surgical staplers recalled over a malformed cover tube press

    Covidien is recalling 3,263 Signia Small Diameter Curved Tip Intelligent Reloads because a manufacturing issue can allow internal components to move during firing, risking uncontrolled motion.

    Product
    Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); CFN: SIGSDL45CTVT;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0482-2026·2025-11-19

    Electrosurgical snares recalled over small holes compromising package sterility

    Olympus is recalling 48,208 Single Use Electrosurgical Snares SD-400 because sterility may be compromised by small holes formed during packaging or transportation.

    Product
    Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use Electrosurgical Snare Model/Catalog Number: SD-400U-10 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and/or cauterization of di
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0474-2026·2025-11-19

    Blunt tip sealers 44 cm recalled over trapped residual material

    Medline is recalling 1,446 reprocessed LigaSure Blunt Tip sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 44cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0467-2026·2025-11-19

    LigaSure Exact dissectors recalled over residual material that may dislodge

    Medline is recalling 4,226 reprocessed LigaSure Exact dissectors, 21 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal LigaSure Exact, Dissector without Nano-Coating 21cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical Cutting And Coagulation Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0458-2026·2025-11-19

    Spinal cord stimulators recalled over loss of programmer communication

    Abbott Medical is recalling 20,715 Eterna spinal cord stimulation implantable pulse generators because the devices may lose communication with the clinician programmer or patient controller.

    Product
    Eterna SCS IPG (Implantable Pulse Generator), Model Number 32400
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0183-2026·2025-11-19

    Tense-X supplement recalled because it contains magnesium salicylate

    Professional Botanicals is recalling 253 bottles of Tense-X capsules because the product contains magnesium salicylate.

    Product
    Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsules. Product Sku: PB207
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0487-2026·2025-11-19

    Oxygenators recalled after a unit failed carbon dioxide transfer requirements

    Medtronic Perfusion Systems is recalling 26 Affinity NT Oxygenators after identifying a unit with decreased CO2 gas transfer rates that did not meet performance requirements.

    Product
    Affinity NT Oxygenator, Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous Reservoir, Product Number 541B
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0498-2026·2025-11-19

    Long nasal feeding tubes recalled from one lot for possible occlusion

    Applied Medical Technology is recalling NutraGlide 6 F-8 F x 90 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.

    Product
    Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0455-2026·2025-11-19

    Bedside patient monitors recalled over batteries that fail as backup power

    GE Healthcare is recalling 7,408 B105P, B125P, B105M, B125M and B155M patient monitors because certain batteries can lose the ability to hold charge, causing a loss of monitoring.

    Product
    B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102 6160000-103 6160000-104 6160000-105 6160001-063 6160001-064 6160001-065 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms 3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0454-2026·2025-11-19

    CARESCAPE ONE monitors recalled over batteries that fail to hold charge

    GE Healthcare is recalling 5,935 CARESCAPE ONE patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.

    Product
    CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Updated 3/19 to add CARESCAPE ONE MBZ101 2087075-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0471-2026·2025-11-19

    Five millimetre blunt tip sealers recalled over trapped residual material

    Medline is recalling two reprocessed LigaSure Blunt Tip sealer/dividers, 5 mm x 37 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal LigaSure Blunt Tip Sealer/Divider, Compatible with FT10 Generator, 5 mm x 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0486-2026·2025-11-19

    VATS lobectomy stapler boxes recalled over a malformed cover tube press

    Covidien is recalling two units of a VATS lobectomy box containing the Signia Small Diameter Curved Tip Intelligent Reload because internal components may move during firing.

    Product
    Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0469-2026·2025-11-19

    Impact vessel sealers recalled over residual material that may dislodge

    Medline is recalling 58,499 reprocessed LigaSure Impact sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.

    Product
    Medline Renewal Ligasure Impact Sealer/Divider NanoCoated, Compatible with FT10 Generator 18cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0477-2026·2025-11-19

    Maryland jaw sealers 44 cm recalled over trapped residual material

    Medline is recalling 9,547 reprocessed LigaSure Maryland Jaw sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0465-2026·2025-11-19

    DigitalDiagnost C90 systems recalled over ceiling carriages resisting vertical movement

    Philips is recalling 223 DigitalDiagnost C90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.

    Product
    DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0464-2026·2025-11-19

    DigitalDiagnost 4 systems recalled over ceiling carriages hard to move

    Philips is recalling 12 DigitalDiagnost 4 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.

    Product
    DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0500-2026·2025-11-19

    Platelet reactivity tests recalled after an uncleared device was distributed

    Accriva Diagnostics is recalling 125 boxes, 3,125 tests, of VerifyNow PRUTest because a device without premarket clearance was incorrectly packaged and distributed.

    Product
    VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0479-2026·2025-11-19

    ACL restoration implants recalled from one lot held in sales stock

    Miach Orthopaedics is recalling 167 BEAR Implants from a single lot, in an action the record says was limited to sales force trunk stock.

    Product
    BEAR Implant (Bridge-Enhanced ACL Restoration); Model/Catalog: 1000;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0466-2026·2025-11-19

    Radiography systems recalled over ceiling carriages that are hard to move

    Philips is recalling 284 Radiography 7300 C systems because some ceiling suspension telescopic carriages may be difficult to move vertically.

    Product
    Radiography 7300 C; Model Number: 712037;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0484-2026·2025-11-19

    Laboratory cuvette arrays recalled over barcodes the analyser cannot read

    Becton Dickinson is recalling 29,760 BD Kiestra Isolate Suspension Cuvette Arrays because formatting errors in the 2D barcodes stop the analyser reading the expiration date.

    Product
    BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E078000·2025-11-18

    Mack Trucks Recalls Certain Vehicles Due to Electronic Control Unit Defect

    Mack Trucks is recalling certain vehicles because electrical noise may cause the electronic control unit to malfunction, potentially disabling safety systems like ABS and increasing crash risk.

    Product
    ELECTRICAL SYSTEM:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V798000·2025-11-18

    2024 Kawasaki Ninja ZX-6R Motorcycles Engine Stall Recall

    Kawasaki is recalling 2024–2026 Ninja ZX-6R motorcycles because a metal crankshaft bushing may seize, causing engine stall and increasing crash risk. Owners are advised not to ride until dealers re-tighten the bushing free of charge.

    Product
    KAWASAKI — KAWASAKI NINJA ZX-6R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V795000·2025-11-17

    Peterbilt 567 and 589 Trucks Recalled for Brake Air Tank Defect

    PACCAR is recalling 2026 Peterbilt 567 and 589 trucks because air tanks have insufficient volume, potentially reducing braking performance.

    Product
    PETERBILT — PETERBILT 589, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V794000·2025-11-17

    Kia K5 fuel tank can expand and melt against hot exhaust

    Kia is recalling certain 2021-2024 K5 vehicles because a damaged check valve can let air into the fuel tank, causing it to expand, contact hot exhaust components and melt.

    Product
    KIA — KIA K5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V796000·2025-11-17

    Hyundai Sonata fuel tank can expand and melt against hot exhaust

    Hyundai is recalling certain 2020-2023 Sonata vehicles because a damaged check valve can let air into the fuel tank, causing it to expand, contact hot exhaust components and melt.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V791000·2025-11-17

    Thor motorhome solar panel mounting brackets can loosen or break

    Thor Motor Coach is recalling certain 2022-2024 Tellaro, Sequence, Twist, Dazzle and other RVs because the solar panel mounting brackets may loosen or break, allowing the panel to detach.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TWIST, TRANQUILITY, DAZZLE, FREEDOM ELITE VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V792000·2025-11-17

    Thor motorhome solar panel adhesive can fail allowing detachment

    Thor Motor Coach is recalling certain 2022-2024 Tellaro, Sequence, Dazzle, Scope, Rize and Twist RVs because the adhesive securing the solar panels to the roof may fail.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH RIZE, TELLARO, DAZZLE, SEQUENCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V797000·2025-11-17

    Hyundai IONIQ 5 front seat belt retractors may not be secured

    Hyundai is recalling certain 2025 IONIQ 5 vehicles because the seat belt retractors for the driver and front passenger seats may not be securely fastened.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V793000·2025-11-17

    Ford E-350 and E-450 engine covers can become excessively hot

    Ford is recalling certain 2021 E-350 and E-450 vehicles that received an incomplete software update under recall 20V795, because the engine cover may become excessively hot.

    Product
    FORD — FORD E-350, E-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V790000·2025-11-17

    Triple E Recalls 2025-2026 Unity RVs Due to Incorrect Seat Belt Labeling

    Triple E is recalling 2025-2026 Unity recreational vehicles because the weight label incorrectly lists a seating capacity of four, while the vehicle is equipped with only two seat belts.

    Product
    TRIPLE E — TRIPLE E UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V789000·2025-11-14

    Plug-in hybrids recalled over battery cell defect that can short internally

    Ford is recalling 20,558 model year 2020-2024 Escape and 2021-2024 Lincoln Corsair plug-in hybrids because a defect in high voltage battery cells may cause an internal short and battery failure.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR PHEV, ESCAPE PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V787000·2025-11-14

    Ford Recalls 2025 Maverick and Escape for Brake Booster Overheating Risk

    Ford is recalling 2025 Maverick and Escape vehicles because an electric brake booster cover may overheat, potentially causing loss of stability control or brake power assist.

    Product
    FORD — FORD ESCAPE, MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V788000·2025-11-14

    Bronco models recalled because the instrument cluster may fail at startup

    Ford is recalling 229,609 model year 2025-2026 Bronco and Bronco Sport vehicles because the instrument panel cluster may fail at startup, hiding warning lights and vehicle speed.

    Product
    FORD — FORD BRONCO SPORT, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26090·2025-11-13

    Power banks and charging stands recalled after overheating fires reported

    About 83,500 Belkin power banks and wireless charging stands are being recalled because the lithium-ion battery can overheat; one US fire and 15 international reports have been received.

    Product
    Portable Power Banks and Wireless Charging Stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26092·2025-11-13

    Home battery systems recalled after overheating smoke and fire reports

    About 10,500 Tesla Powerwall 2 units are being recalled because battery cells can cause the unit to stop working and overheat; 22 overheating reports include five fires.

    Product
    Certain Tesla Powerwall 2 AC Battery Power System
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E076000·2025-11-13

    Eaton Recalls Differentials With Oversized Gear Teeth That May Lock

    Eaton is recalling specific differentials that may lock due to oversized gear teeth, increasing crash risk. Owners should not drive until repaired.

    Product
    POWER TRAIN:DRIVELINE:DIFFERENTIAL UNIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V781000·2025-11-13

    Trucks recalled because a clogged valve can keep the brakes engaged

    International Motors is recalling 1,303 model year 2023-2026 LT and 2024-2025 RH trucks because a clogged Hill Start Assist exhaust port may delay or prevent release of the service brakes.

    Product
    INTERNATIONAL — INTERNATIONAL LT, RH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V784000·2025-11-13

    Fifth wheel trailers recalled over propane lines that can crack and leak

    Grand Design RV is recalling 95 model year 2022-2023 Solitude and 2023 Momentum fifth wheel trailers because loose or missing fasteners can let the refrigerator move and crack the propane line.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM, SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26086·2025-11-13

    Silicone activity toys recalled after a child gagged and choked on one

    About 117,500 Zippee children's silicone activity toys are being recalled because the spherical string ends can reach the back of the throat; one child gagged, vomited and choked.

    Product
    Zippee Activity Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V782000·2025-11-13

    New Way 2025 Loader Trucks Recalled for CNG Fuel Leak Risk

    NHTSA is recalling 2025 New Way side and front loader trucks because CNG fuel system valves may crack and leak, increasing fire risk.

    Product
    NEW WAY — NEW WAY SIDE LOADER, FRONT LOADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V785000·2025-11-13

    Accord Hybrids recalled because a control module reset can cut drive power

    Honda is recalling 256,603 model year 2023-2025 Accord Hybrid vehicles because a software error may reset the integrated control module CPU while driving, causing a loss of drive power.

    Product
    HONDA — HONDA ACCORD HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26089·2025-11-13

    Coin battery packs recalled for missing child resistant packaging and warnings

    About 32,600 Great Lakes Select button cell and coin battery packs are being recalled because they lack the child-resistant packaging and warning labels required under Reese's Law.

    Product
    Great Lakes Select Button Cell and Coin Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26088·2025-11-13

    Trek and Electra bicycles recalled because coaster brakes can fail to engage

    About 68,000 Trek and Electra bicycles with coaster brakes, plus replacement rear wheels, are being recalled because the coaster brakes can fail to engage.

    Product
    Trek and Electra-branded Bicycles with Coaster Brakes and Replacement Rear Wheels with Coaster Brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V783000·2025-11-13

    School buses recalled because the weight rating may be exceeded when full

    International Motors is recalling 142 model year 2023-2027 IC Bus CESB school buses because the bus may exceed its Gross Vehicle Weight Rating when fully occupied with full tanks.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V780000·2025-11-13

    Forest River Bus Recalls Transit Buses With Defective Wheelchair Restraints

    Forest River Bus is recalling 2025-2026 transit buses because wheelchair restraints may fail to lock, increasing injury risk.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS GLAVAL ENTOURAGE, ELDORADO, ELKHART COACH, FOREST RIVER VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V779000·2025-11-13

    Forest River Recalls School Buses with Defective Wheelchair Restraints

    Forest River Bus is recalling certain 2025-2027 school buses because wheelchair restraints may fail to lock, increasing injury risk.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS COLLINS SCHOOL BUS, TRANS TECH SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26085·2025-11-13

    Doll sets recalled over button cell batteries children can easily reach

    About 380 Bettina Doll Sets with Magic Light Unicorn are being recalled because the unicorn's battery compartment lets children easily access button cell batteries.

    Product
    Bettina Doll Set with Magic Light Unicorn
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0153-2026·2025-11-12

    Farm shell eggs recalled over potential Salmonella contamination in New York

    Jacob King is recalling approximately 15 dozen in-shell chicken eggs distributed from a farm in Addison, New York, over potential Salmonella. The FDA has classified it Class I.

    Product
    In-shell chicken eggs distributed on Jacob King's farm in Addison, NY
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-0156-2026·2025-11-12

    Soft taco dinner kits recalled over an undeclared milk allergen

    Teasdale Foods is recalling 3,654 cases, 21,924 units, of Casa Mamita Soft Taco Dinner Kit sold at ALDI over undeclared milk. The FDA has classified the recall as Class I.

    Product
    Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g), UPC: 4099100318715, DIST. & SOLD EXCLUSIVELY BY: ALDI BATAVIA, IL 60510 Product consists of 10 flour tortillas, 1 sauce packet, and 1 seasoning packet within a carton; 6 cartons are packed into a mixed case with 6 addition
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·H-0171-2026·2025-11-12

    Repackaged shell eggs recalled over potential Salmonella contamination in retail brands

    Eggs Unlimited is recalling 92,476 units of shell eggs sold under Big Y, Simple Truth, Stater Bros, That's Smart, Lindsey's Gold and Marketside labels over potential Salmonella.

    Product
    Big Y Brown Jumbo A 12ct Eggs; UPC: 018894319146 Simple Truth Cage Free Brown Large AA 12ct; UPC: 011110797698 Stater Bros Cage Free Large AA 18ct; 074175001650 That's Smart Cage Free Large AA 60ct; 193476006192 Lindsey s Gold Free Range Brown Large A 12ct; 860011334408 Marketsid
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·H-0170-2026·2025-11-12

    Pastured large eggs recalled over potential Salmonella contamination in Texas

    Kenz Henz is recalling 16,400 dozen Pastured Grade AA Large Eggs distributed in Texas because the eggs may be contaminated with Salmonella. The FDA has classified the recall as Class I.

    Product
    " Product Name: Pastured Grade AA Large Eggs " Product Description: Egg Carton, 12 eggs per dozen " Pack/Julian Date(s): Julian date 241(Aug 30) to 244 (Sep 2) and 246 (Sep 4) to 247 (Sep 5), Best by Dates 10/11 to 10/14/25 and 10/16 to 10/17.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-0155-2026·2025-11-12

    Crunchy taco dinner kits recalled over an undeclared milk allergen

    Teasdale Foods is recalling 336 cases, 4,032 units, of Giant/Martin's Crunchy Taco Dinner Kit over undeclared milk. The FDA has classified the recall as Class I.

    Product
    Giant/Martin's Crunchy Taco Dinner Kit, Net Wt 9.4 OZ (266g), UPC: 068826757516, DISTRIBUTED BY: ADUSA DISTRIBUTION, LLC SALISBURY, NC 28147 Product consists of 12 taco shells, 1 sauce packet, and 1 seasoning packet within a carton; packed 12 cartons per case
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Devices)·Z-0427-2026·2025-11-12

    Insulin pumps recalled over false vibration motor failure stopping delivery

    Tandem Diabetes Care is recalling 17,745 Tandem Mobi insulin pumps because a software issue can trigger a false vibration motor failure that halts insulin delivery. The FDA classified it Class I.

    Product
    Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to deliver insulin from within a disposable cartridge, through an infusion set,
    Category
    Medical Device
    Distribution
    53 states
  • CriticalFDA (Devices)·Z-0373-2026·2025-11-12

    Eleven millimetre cranial perforators recalled over inadequate welds

    Integra LifeSciences is recalling 16,251 CODMAN Disposable Perforators, 11mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.

    Product
    CODMAN Disposable Perforator 11mm. Cranial Perforator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0374-2026·2025-11-12

    Cranial perforators recalled as inadequate weld recall expands to smaller sizes

    Integra LifeSciences is recalling 5,109 CODMAN Disposable Perforators, 9mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.

    Product
    CODMAN Disposable Perforator 9mm. Cranial Perforator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0147-2026·2025-11-12

    Frozen crab paste recalled over undeclared fish soy and wheat

    New York Mutual Trading is recalling about 21 cases of frozen crab paste sold to restaurants over undeclared fish, soy and wheat. The FDA has classified the recall as Class I.

    Product
    Frozen Crab Paste; 3.5 OZ (100g); Imported by Mutual Tading Co. Inc. UPC# 72546723040 "Not for retail Sale" Frozen Crab Paste IM-2 in w/Tray; 500g; Imported by Mutual Trading Co. Inc. UPC# 72546607852 "Not for retail Sale" Frozen Crab Paste; 17.6 OZ (500g); Imported by Mutual Ta
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·25V777000·2025-11-12

    Audi SUVs recalled because seat belt buckles may be missing a rivet

    Volkswagen Group of America is recalling certain 2025 Audi Q7, Q8, SQ8 and RS Q8 vehicles because the front seat belt buckles may be missing a rivet that secures the buckle to the stalk.

    Product
    AUDI — AUDI SQ8, RS Q8, Q7, Q8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0155-2026·2025-11-12

    Pain relief caplets recalled because the box names the wrong drug

    Aero Healthcare is recalling two lots of AERO TAB caplets because the outer box states acetaminophen and caffeine while the inner pouch correctly states aspirin and caffeine.

    Product
    AEROTAB PAIN RELIEVER — AEROTAB PAIN RELIEVER (PAIN RELIEVER)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0163-2026·2025-11-12

    Easy peel deveined shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 1,800 cases of AquaStar 13/15 Raw Shrimp Easy Peel Deveined, sold at Publix, because the shrimp may be contaminated with Cesium-137.

    Product
    AquaStar 13/15 Raw Shrimp Easy Peel Deveined, net wt. 2 lbs. UPC 731149654051. Product was sold at Publix.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0159-2026·2025-11-12

    Raw shrimp skewers recalled over potential Cesium-137 contamination

    AquaStar is recalling 5,220 cases of AquaStar Raw Peeled Tail-on Shrimp Skewers because the shrimp may be contaminated with Cesium-137.

    Product
    AquaStar Raw Peeled Tail-on Shrimp Skewers, net wt. 1.25lbs. UPC 731149390010. Product is packaged in a printed bag with a black top and blue bottom and printed pictures of the skewers inside.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0152-2026·2025-11-12

    Frozen coconut bars recalled over sulfites undeclared on the product label

    Que Rikura's Products is recalling 31,953 cases of 4 oz frozen coconut bars distributed in Florida because sulfites are undeclared on the product label.

    Product
    Frozen Coconut bar Net wt. 4oz (113g) single bars packed in a plastic cup. UPC: 61058590845. Crafted by Fruitique International Miami USA 33016. Phone 1(888)960-6024
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·25V776000·2025-11-12

    Winnebago Recalls 2025-2026 Micro Minnie Travel Trailers Due to Fire Risk

    Winnebago is recalling 2025-2026 Micro Minnie travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire risk.

    Product
    WINNEBAGO — WINNEBAGO MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0166-2026·2025-11-12

    Strawberry cheesecake ice cream recalled over foil fragments in brown sugar

    Ice Cream Factory is recalling 979 cases and 313 tubs of Strawberry Cheesecake ice cream after aluminum foil and packaging fragments were found in a brown sugar ingredient.

    Product
    Strawberry Cheesecake Ice Cream with graham crackers swirl, 12 oz pack, Single Cup Net Wt: 8.75oz, Case of 12 Strawberry Cheesecake with graham cracker swirl, 2.5-gal Tub, Net Weight 14 pounds Labels read in part as "Ice Cream Factory, Distributed by Ice Cream Factory 1201 Ice C
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·H-0160-2026·2025-11-12

    Best Yet frozen shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 9,900 cases of Best Yet Frozen Raw EZ-Peel White Shrimp across multiple counts because the shrimp may be contaminated with Cesium-137.

    Product
    Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700282 Best Yet Frozen Raw EZ-Peel White Shrimp 21/25 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700286 Best Yet Frozen Raw EZ-Peel White Shrimp 26/30 (net wt. 1 lbs/pkg; 10
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0417-2026·2025-11-12

    Dental implant screws recalled because the wrong screw was packaged

    Prismatik Dentalcraft is recalling 208 Inclusive Titanium Screws because an incorrect titanium screw was packaged with the dental implant.

    Product
    Brand Name: Inclusive Product Name: Inclusive Titanium Screw compatible with: Biomet 3i" Certain 3.4/4.1/5.0/6.0 mm Model/Catalog Number: 70-1047-COM0117
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Devices)·Z-0422-2026·2025-11-12

    Dialysis catheter trays recalled over seal integrity of header bag packaging

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays, 12 Fr x 16 cm, over a potential issue with the seal integrity of the header bag packaging.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 16 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0165-2026·2025-11-12

    Peeled tail on shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 2,916 cases of Publix Large Shrimp Peeled & Deveined Tail On 31/40 because the shrimp may be contaminated with Cesium-137.

    Product
    Publix Large Shrimp Peeled & Deveined Tail On 31/40, net wt. 1.5 lbs. UPC 041415067455. Product was sold at Publix.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0167-2026·2025-11-12

    Bakery graham pieces recalled over foil fragments in brown sugar

    Ice Cream Factory is recalling 255 ten-pound boxes of Bakery Graham Pieces after aluminum foil and packaging fragments were found in a brown sugar ingredient.

    Product
    Bakery Graham Pieces, 10 LB Label reads in part as "Ice Cream Factory, #10 Graham Pieces, Distributed by Ice Cream Factory, 1201 Ice Cream Way, Lebanon, MO 65536"
    Category
    Food
    Distribution
    29 states
  • HighFDA (Devices)·Z-0433-2026·2025-11-12

    Stereotactic frames recalled because paint flakes may enter the wound

    Elekta is recalling 338 Leksell Vantage Stereotactic System components because paint flakes from the engravings may separate and could inadvertently enter the wound.

    Product
    Brand Name: Leksell Stereotactic System Product Name: Leksell Vantage Stereotactic System Software Version: n/a Product Description: The Intended Purpose of Leksell¿ Vantage" Stereotactic System is target localization and fixation of the patient head in a coordinate system in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0425-2026·2025-11-12

    Straight extension catheter trays 24 cm recalled over header bag seals

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions and IC components, 12 Fr x 24 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 24 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0153-2026·2025-11-12

    Clomipramine 50 mg capsules recalled over nitrosamine above the intake limit

    Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 50 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0164-2026·2025-11-12

    Extra large peeled shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 1,458 cases of Publix Extra Large Shrimp Easy to Peel Deveined 21/25 because the shrimp may be contaminated with Cesium-137.

    Product
    Publix Extra Large Shrimp Easy to Peel Deveined 21/25, net wt. 1.5 lbs. UPC 041415064454. Product was sold at Publix.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0432-2026·2025-11-12

    Hip bipolar heads recalled over packaging that may compromise sterility

    Total Joint Orthopedics is recalling 103 Klassic BiPolar Heads over a potential packaging issue that could compromise the sterile barrier and present a risk of infection if implanted.

    Product
    Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic BiPolar Head, 41 mm OD, 22 mm Head; 3205.42.022 Klassic BiPolar Head, 42 mm OD, 22 mm Head; 3205.43.022 Klassic BiPolar Head, 43 mm OD, 22 mm Head; 3205.44.028 Klassic BiPolar Head, 44 mm OD, 28 mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0157-2026·2025-11-12

    Colossal EZ peel shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 5,400 cases of Kroger Raw Colossal EZ Peel Shrimp because the shrimp may be contaminated with Cesium-137.

    Product
    Kroger Raw Colossal EZ Peel Shrimp, net wt. 2lbs., UPC 20011110643906. Product is packaged in transparent printed bag with a blue band on the top with yellow and red details.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0420-2026·2025-11-12

    Navigation adapters recalled because the system may miss its specified accuracy

    Integra LifeSciences is recalling 1,198 TruDi Navigation System Multi Instrument Adapters because certain revision combinations may not meet specified accuracy for locating a device in the anatomy.

    Product
    TruDi¿ Navigation System - Multi Instrument Adapter; - Manufacturer's Product Number (Catalog Number): EM-2025-000F Rev 00 or Rev 01;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0154-2026·2025-11-12

    Clomipramine 75 mg capsules recalled over nitrosamine above the intake limit

    Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 75 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0152-2026·2025-11-12

    Clomipramine 25 mg capsules recalled over nitrosamine above the intake limit

    Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 25 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0154-2026·2025-11-12

    Ground ginger recalled over elevated levels of lead in one lot

    Eagle Spice and Extract is recalling 2,476 units of Eagle Spice Ground Ginger 16 oz because the product contains elevated levels of lead.

    Product
    Eagle Spice Ground Ginger 16 oz.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0429-2026·2025-11-12

    Chemistry analyzers recalled over gantry defect that pauses the instrument

    Beckman Coulter is recalling 657 UniCel DxI 800 analyzers because defective gantry sub-components can cause a z-axis motion error that halts the analyzer and delays results.

    Product
    Beckman Coulter UniCel DxI 800, Part Numbers: 973100, A71456; Photometric Chemistry Analyzer
    Category
    Medical Device
    Distribution
    0 states

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