The Recall Desk

Archive

February 2026 recalls

554 recalls were announced in February 2026.

What the numbers show

Critical
49
Severe
59
High
333
Moderate
106
Low
7

Of the 554 recalls this month scored against our rubric, 9% are Critical, 11% are Severe.

Which agencies issued them

101–200 of 554

  • HighFDA (Devices)·Z-1411-2026·2026-02-25

    LVAD driveline trays recalled over sterilization equipment calibration issues

    Medline is recalling 9,720 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) LVAD DRIVELINE TRAY, Model Number: DM1035A; 2) LVAD DRIVELINE TRAY, Model Number: DM1035; 3) CENTRAL LINE DRESSING CHANGE TRAY, Model Number: DT8670A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1410-2026·2026-02-25

    Admit kits recalled over sterilization equipment calibration issues

    Medline is recalling 1,070 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) ADMIT KIT, Model Number: DYKA1343A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1424-2026·2026-02-25

    Surgical gowns recalled over sterilization equipment calibration issues

    Medline is recalling 70,376,042 units of surgical gowns because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Surgical Gowns: 1) GOWN,NONRNF,L,30/CS, Model Number: DYNJP2001; 2) GOWN,SIRUS,NONRNF,SETINSLV,L,20/CS, Model Number: DYNJP2001S; 3) GOWN,ECLIPSE,NONRNF,XL,ST,30/CS, Model Number: DYNJP2002; 4) GOWN,SIRUS,NONRNF,SETINSLV,XL,20/CS, Model Number: DYNJP2002S; 5) GOW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1364-2026·2026-02-25

    Medihoney Calcium Alginate Dressings Recalled Due to Potential Sterile Barrier Breach

    Integra LifeSciences Corp. is recalling certain Medihoney Calcium Alginate dressings because packaging failures could lead to a breach in the sterile barrier.

    Product
    MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers: (1) 31012, (2) 31022, (3) 31045. MEDIHONEY CALCIUM ALGINATE DRESSING WITH ACTIVE LEPTOSPERMUM HONEY supports and aids autolytic debridement and is indicated for the management of moderately to heavily
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1408-2026·2026-02-25

    PPE kits recalled over sterilization equipment calibration issues

    Medline is recalling 7,575 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) PPE KIT, Model Number: DYK1011945P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1398-2026·2026-02-25

    Lithotomy packs recalled over sterilization equipment calibration issues

    Medline is recalling 808 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) LITHOTOMY PACK, Model Number: DYNJ83185; 2) LITHOTOMY PACK, Model Number: DYNJ83185A;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26C002000·2026-02-25

    Evenflo Recalls LiteMax Child Seats Due to Incorrect Spanish Manual

    Evenflo is recalling LiteMax Factory Select child seats because the Spanish manual lists incorrect weight and height limits, which could lead to improper restraint.

    Product
    EQUIPMENT:OTHER:OWNERS/SERVICE/OTHER MANUAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1373-2026·2026-02-25

    Thunderbeat Type S devices removed after continued adverse event reports

    Olympus is removing the Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S from the market, stating the action is due to continued reports of adverse events.

    Product
    Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1401-2026·2026-02-25

    Line insertion kits recalled over sterilization equipment calibration issues

    Medline is recalling 553 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) KIT ACES INSERT PEG, Model Number: DYKMBNDL130; 2) KIT ACES INSERT PEG, Model Number: DYKMBNDL130A; 3) KIT ACES INSERT PERCUTANEOUS T, Model Number: DYKMBNDL4; 4) NICU LINE CHANGE TRAY, Model Number: LC295; 5) OSC SHERMAN KNEE ARTHRO BASIC, M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0537-2026·2026-02-25

    Liquid Dietary Supplements Recalled Due to Undeclared Milk Allergen

    Pure Solutions, Inc. is recalling Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset because the labels do not declare milk as an allergen.

    Product
    Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid dietary supplement, Glass bottle with dropper cap. (Individual 1 fl oz bottles (not sold in case lots)
    Category
    Food
    Distribution
    36 states
  • HighFDA (Devices)·Z-1368-2026·2026-02-25

    Infusion pumps recalled after being released without full testing

    Baxter Healthcare is recalling 5 Spectrum IQ Infusion Pumps because they were released without full testing being performed, including occlusion alarm testing.

    Product
    Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Description: Infusion Pump, one unit per carton Component: N/A
    Category
    Medical Device
    Distribution
    1 state
  • ModerateNHTSA·26V110000·2026-02-25

    2026 Toyota Corolla front headlights missing aim markings

    Toyota is recalling certain 2026 Corolla vehicles due to missing headlight aim markings that can result in improperly aimed headlights, increasing crash risk and glare for oncoming drivers.

    Product
    TOYOTA — TOYOTA COROLLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V108000·2026-02-24

    Newmar motorhome hood stop adhesive may fail allowing detachment in transit

    Newmar is recalling certain 2018-2026 Bay Star and Bay Star Sport motorhomes because the hood stops mounting adhesive may fail, allowing the hood stop to detach while the vehicle is in transit.

    Product
    NEWMAR — NEWMAR BAY STAR, BAY STAR SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V107000·2026-02-24

    Newmar Recalls 2026 Freedom Aire Motorhomes Due to Wiring Defect

    Newmar is recalling 2026 Freedom Aire motorhomes because a wiring error may cause the heating system to activate unintentionally, producing harmful gas.

    Product
    NEWMAR — NEWMAR FREEDOM AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V109000·2026-02-24

    Thomas Built Buses Recalls 2027 Saf-T-Liner C2 School Buses for Heater Hose Defect

    Daimler Trucks North America is recalling 2027 Thomas Built Buses Saf-T-Liner C2 school buses because a heater hose may rupture, causing hot coolant to leak into the passenger compartment.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V105000·2026-02-23

    Kia Telluride front seat back frames may not restrain occupants

    Kia is recalling certain 2025 Telluride vehicles with power front seats because a manufacturing error may leave the driver and passenger seat back frame assemblies unable to properly restrain occupants in a crash.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V106000·2026-02-23

    Subaru Recalls 2025-2026 Hybrid Vehicles for Fuel Cap Seal Defect

    Subaru is recalling 2025 Forester and 2026 Crosstrek hybrids because a faulty fuel cap seal may cause fuel to spill when the tank is near full and temperatures rise.

    Product
    SUBARU — SUBARU FORESTER HYBRID, CROSSTREK HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·006-2026·2026-02-22

    Rosina Recalls Frozen Meatballs Due To Possible Metal Contamination

    Rosina Food Products is recalling approximately 9,462 pounds of frozen Bremer meatballs due to possible metal contamination. The products were distributed to Aldi locations nationwide.

    Product
    Rosina Food Products, Inc. — Rosina Food Products, Inc. Recalls Ready-To-Eat Frozen Meatball Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V103000·2026-02-20

    Volvo EX30 high voltage battery may short circuit and overheat

    Volvo is recalling certain 2025 EX30 vehicles because the high voltage battery may experience a short circuit and overheat. Owners are advised to limit charging to a maximum of 70%.

    Product
    VOLVO — VOLVO EX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V100000·2026-02-20

    Rossmonster Recalls 2023-2025 Baja Motorhomes Due to Brake Line Routing

    Rossmonster is recalling 2023-2025 Baja Ex and Baja LX motorhomes because incorrectly routed front brake lines may contact tires, causing leaks and reduced braking performance.

    Product
    ROSSMONSTER — ROSSMONSTER BAJA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V098000·2026-02-20

    Demers Ambulances Recall FXP174 Models for Seat Floor Strength Defect

    Braun Industries is recalling 2025-2026 Demers FXP174 ambulances because the floor may not securely hold seats during a crash, increasing injury risk.

    Product
    Demers Ambulances — Demers Ambulances FXP174
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V099000·2026-02-20

    Mercedes-Benz eSprinter Recalled for Insufficient Pedestrian Warning Sounds

    Daimler Vans USA is recalling 2025 Mercedes-Benz eSprinter vehicles because they fail to make sufficient pedestrian warning sounds when in reverse, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ESPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V104000·2026-02-20

    Ford Vehicles Recalled for Integrated Trailer Module Software Defect

    Ford is recalling multiple 2021–2026 trucks, vans, and sport utility vehicles because the integrated trailer module may lose communication with the vehicle when towing, causing loss of trailer brake and turn signal lights or brake function.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR, F-600 SD, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V102000·2026-02-20

    Orange EV Recalls T-Series and e-TRIEVER Trucks for Door Lock Defect

    Orange EV is recalling 2018-2026 T-Series and e-TRIEVER trucks because driver's side door handles may lack a lock, potentially failing federal safety standards.

    Product
    ORANGE EV — ORANGE EV T-SERIES ELECTRIC TRUCK, E-TRIEVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2026·2026-02-19

    Sobico USA Recalls Frozen Siluriformes Fish Imported Without Reinspection

    Sobico USA LLC is recalling approximately 13,464 pounds of frozen, raw Siluriformes fish products imported from Vietnam without the benefit of import reinspection.

    Product
    Sobico USA LLC Recalls Siluriformes Fish Products Imported Without The Benefit of Import Reinspection
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·26V097000·2026-02-19

    Range Rover panoramic sunroof side trim may not be properly secured

    Land Rover is recalling certain 2023-2026 Range Rover and Range Rover Sport vehicles because the panoramic sunroof side finisher trim may not be properly secured and can detach.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V096000·2026-02-19

    BMW Recalls Multiple Models for Air Conditioning Wiring Fire Risk

    BMW is recalling specific 2023-2026 models because the air conditioning wiring harness may be damaged during filter replacement, increasing the risk of a fire.

    Product
    BMW — BMW I7 EDRIVE50, I7 XDRIVE60, I5 EDRIVE40, I5 XDRIVE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2026·2026-02-19

    Ajinomoto Recalls Frozen Chicken Fried Rice Due to Glass Contamination

    Ajinomoto Foods North America is recalling frozen chicken fried rice products due to possible glass contamination. No injuries have been reported.

    Product
    Ajinomoto Foods North America — Ajinomoto Foods North America, Inc. Recalls Chicken Fried Rice Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·26272·2026-02-19

    Magnetic balls and rods sets recalled over a deadly choking hazard

    About 782 Huaker Magnetic Balls and Rods sets are being recalled because they contain small balls and are intended for children under three years of age.

    Product
    Huaker Magnetic Balls and Rods Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E008000·2026-02-19

    Prevost Recalls Exterior Driver Side Mirrors Due to Detachment Risk

    Prevost is recalling specific exterior driver side mirrors that may detach due to excessive play, posing a visibility and road hazard risk.

    Product
    VISIBILITY:REARVIEW MIRRORS/DEVICES:EXTERIOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26275·2026-02-19

    Children's footed sleepwear recalled over the flammability standard for sleepwear

    About 211,520 MCS and Lullaby Lane one-piece footed sleepwear items sold at Meijer are being recalled because they violate the mandatory flammability standard for children's sleepwear.

    Product
    Meijer one-piece footed 12-, 18-and 24-month children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V095000·2026-02-19

    Prevost Recalls 2026 H3-45 Buses Due to Mirror Detachment Risk

    Prevost is recalling 2026 H3-45 and H3-45 VIP buses because aftermarket driver-side mirrors may detach, creating a road hazard.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26276·2026-02-19

    Book nook decorations recalled over an accessible spare coin battery

    About 1,770 Prismatic 3D Prints Book Nooks with Lights are being recalled because the spare lithium coin battery can be easily accessed by children.

    Product
    Prismatic 3D Prints Book Nooks with Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26277·2026-02-19

    Youth helmets recalled over failure to meet positional stability requirements

    About 3,295 SAMIT youth multi-purpose helmets are being recalled because they do not comply with the positional stability and certification requirements of the bicycle helmet standard.

    Product
    SAMIT Youth Multi-Purpose Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26274·2026-02-19

    LED balloon lights recalled over easily accessible button cell batteries

    About 3,400 JJGoo LED Balloon Lights are being recalled because children can easily access the button cell batteries and the lights lack the warnings required by Reese's Law.

    Product
    JJGoo LED Balloon Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0487-2026·2026-02-18

    White truffle hummus recalled over undeclared sesame in the product

    Carrot Top Kitchens is recalling 12 units of White Truffle Hummus, 8 oz, because it contains undeclared sesame.

    Product
    Carrot Top Kitchens White Truffle Hummus; contains chickpeas, tahini, truffle oil, lemon, salt; 8 oz.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-1322-2026·2026-02-18

    Reprocessed electrophysiology catheters recalled over residual material particles

    Medline is recalling 48 reprocessed St. Jude Supreme and Response diagnostic electrophysiology catheters because these lots may contain small particles of residual material.

    Product
    Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology Catheters: St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 2-5-2mm 401211RH 401222RH 401223RH 401226RH 401227RH 401260RH 401261RH 401306RH 401309RH 401312RH 401430RH 40143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0489-2026·2026-02-18

    Lime ginger hummus recalled over undeclared sesame in the product

    Carrot Top Kitchens is recalling 12 units of Lime Ginger Hummus, 8 oz, because it contains undeclared sesame.

    Product
    Carrot Top Kitchens Lime Ginger Hummus; contains chickpeas, tahini, fresh ginger, lime juice & zest, salt; 8 oz.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-1323-2026·2026-02-18

    Reprocessed ViewFlex ICE catheters recalled over residual material particles

    Medline is recalling 650 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0353-2026·2026-02-18

    UDENYCA syringes recalled after cartons were stored at room temperature

    McKesson is recalling 116 cartons of UDENYCA pegfilgrastim-cbqv injection because they were stored in a controlled room temperature environment instead of the required refrigerated environment.

    Product
    UDENYCA — UDENYCA (PEGFILGRASTIM-CBQV)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1325-2026·2026-02-18

    Reprocessed AcuNav catheters recalled over residual material particles inside

    Medline is recalling 511 reprocessed Siemens ACUSON AcuNav diagnostic ultrasound catheters because these lots may contain small particles of residual material.

    Product
    Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav Ultrasound Catheter, Use on GE Systems 10135910RH; 10043342RH ACUSON AcuNav Ultrasound Catheter, Use on Siemens Systems 10135936RH, 08255790RH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0491-2026·2026-02-18

    Mini beignets recalled over undeclared hazelnut in the filled product

    Costco Wholesale is recalling 8,073 packages of Kirkland Signature Mini Beignets filled with Caramel over undeclared hazelnut.

    Product
    Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged in a clear clamshell container. ALLERGENS INFORMATION: CONTAINS WHEAT, EGG, MILK, SOY. Distributed by Costco Wholesale Corp. PO Box 34535 Seattle, WA.
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Devices)·Z-1321-2026·2026-02-18

    Reprocessed Livewire catheters recalled over residual material particles

    Medline is recalling 41 reprocessed Livewire steerable diagnostic electrophysiology catheters because these lots may contain small particles of residual material.

    Product
    Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters: Livewire Steerable Electrophysiology Catheter,10 Elec. 2-5-2mm 401582RH 401940RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-10-2mm 401904RH; Livewire Steerable Electrophysiology Cath
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1319-2026·2026-02-18

    Reprocessed Webster CS catheters recalled over residual material particles

    Medline is recalling 228 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer BD710DF282RRH BD710FJ282RRH; Webster CS Catheter 10 Electrodes, 2-8-2mm S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0485-2026·2026-02-18

    Lemon and garlic hummus recalled over undeclared sesame in the product

    Carrot Top Kitchens is recalling 12 units of Lemon & Garlic Hummus, 8 oz, because it contains undeclared sesame.

    Product
    Carrot Top Kitchens Lemon & Garlic Hummus; contains chickpeas, tahini, lemon juice & zest, garlic, salt; 8 oz.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-1324-2026·2026-02-18

    Reprocessed ultrasound catheters recalled over residual material particles inside

    Medline is recalling 94 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on GE Systems 10439072RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on Siemens Systems 10438577RH; Bios
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0486-2026·2026-02-18

    Sundried tomato hummus recalled over undeclared sesame in the product

    Carrot Top Kitchens is recalling 12 units of Sundried Tomato and Caper Hummus, 8 oz, because it contains undeclared sesame.

    Product
    Carrot Top Kitchens Sundried Tomato and Caper Hummus; contains chickpeas, sundried tomatoes, tahini, capers, vinegar, salt; 8 oz.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-0488-2026·2026-02-18

    Cherry pepper hummus recalled over undeclared sesame in the product

    Carrot Top Kitchens is recalling 12 units of Cherry Pepper Hummus, 8 oz, because it contains undeclared sesame.

    Product
    Carrot Top Kitchens Cherry Pepper Hummus; contains chickpeas, tahini, pickled cherry peppers, vinegar, garlic, salt; 8 oz.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-1320-2026·2026-02-18

    Reprocessed Inquiry catheters recalled over residual material particles inside

    Medline is recalling 311 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH; Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm 81202RH; Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1313-2026·2026-02-18

    Adult intubation trays recalled over a smaller catheter packed inside

    Medline is recalling 130 Adult Intubation Trays because an 8 Fr suction catheter may have been packed in place of the required 14 Fr catheter.

    Product
    Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0323-2026·2026-02-18

    Testosterone 100mg single pellets recalled over potential metal particulate

    Asteria Health is recalling 153,498 pellets of Testosterone, 100 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 100 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC:79559-1100-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0333-2026·2026-02-18

    Acyclovir injection bags recalled over a lack of assurance of sterility

    Fresenius Kabi Compounding is recalling 1,057 bags of acyclovir sodium 200 mg in 100 mL sodium chloride injection over a lack of assurance of sterility.

    Product
    acyclovir sodium, 200 mg, 200mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, For Intravenous Use, Single-Use Bag, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-035-56
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0521-2026·2026-02-18

    Liquid supplement shots recalled over possible coliforms and E. coli

    TKS Co-pack Manufacturing is recalling 780 bottles of Aonic Complete His liquid dietary supplement over possible coliforms, E. coli and Pseudomonas aeruginosa contamination.

    Product
    Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, induction sealed closed with plastic lid. Each bottle is a serving intended to be taken orally as a dietary supplement. Sipping unit: two 15 count decorated boxes
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1338-2026·2026-02-18

    Transport bag kits recalled over a Tyvek bag seal issue

    AVID Medical is recalling 1,500 Halyard Transport Bag Kits because a Tyvek bag seal issue may compromise the sterility of the kit.

    Product
    Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1312-2026·2026-02-18

    Suction catheter kits recalled over a smaller catheter packed inside

    Medline is recalling 141,971 of its 14 Fr Suction Catheter Kits because an 8 Fr catheter may have been packed in place of the required 14 Fr catheter.

    Product
    Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0308-2026·2026-02-18

    Estradiol 10mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 24,099 pellets of ESTRADIOL, 10 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 10 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3010-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0498-2026·2026-02-18

    Artisan dark chocolate recalled over undeclared milk in the ingredients

    Cacao Art is recalling 128 Crunchy Caramel artisan dark chocolate bars because the product contains butter but milk is not declared in the ingredients or a contains statement.

    Product
    Crunchy Caramel artisan dark chocolate with crunch brown sugar caramel pieces 60% Cacao, NET WT 2 oz (60g), Ingredients *Cocoa Butter, Soy Lecithin (Emulsifier), Butter (Cream, Natural Flavor) CONTAINS: SOY. Garcia Nevett chocolatier de miami, packaged in plastic envelope insid
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0506-2026·2026-02-18

    Punjabi pinni recalled because milk is undeclared in the ingredient statement

    Karison Foods & Snacks is recalling 230 cases of Karison brand Punjabi Pinni, 12 oz, because the product contains milk which is undeclared in the ingredient statement.

    Product
    Karison brand PUNJABI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00215 4; Distributed By: Karison Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that p
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0504-2026·2026-02-18

    Peanut butter and jam packs recalled over blue plastic pieces

    Ventura Foods is recalling 379 cases of Poco Pac creamy peanut butter and strawberry jam after the firm found pieces of blue plastic in a filter during production.

    Product
    CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/STRAWBERRY JAM NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328 CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/STRAWBERRY JAM NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328
    Category
    Food
    Distribution
    40 states
  • HighFDA (Devices)·Z-1327-2026·2026-02-18

    Catheter securement dressing kits recalled over open swabstick seals

    Medline is recalling 1,350 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG, Kit SKU DYNDC3109
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1344-2026·2026-02-18

    Azurion 3 M12 systems recalled over tables that may move unexpectedly

    Philips is recalling 291 units of the Azurion 3 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0505-2026·2026-02-18

    Besan laddoo recalled because milk is undeclared in the ingredient statement

    Karison Foods & Snacks is recalling 230 cases of Karison brand Besan Laddoo, 12 oz, because the product contains milk which is undeclared in the ingredient statement.

    Product
    Karison brand BESAN LADDOO; NET WT. 12 oz.; Ingredients: Gram Flour, Butter, Sugar, Zero Trans Fat Vegetable Shortening, Almonds, Cardamom; UPC: 8 9730700240 6; Distributed By: Karson Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility t
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1350-2026·2026-02-18

    Azurion 5 M12 systems recalled over tables that may move unexpectedly

    Philips is recalling 326 units of the Azurion 5 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1330-2026·2026-02-18

    Vascular access kits and trays recalled over open swabstick seals

    Medline is recalling 21,854 units of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    1) UNIVERSAL KIT, Kit SKU DT22010B; 2) VAD ACCESS KIT, Kit SKU DT22790C; 3) VAD ACCESS KIT, Kit SKU DT22790C; 4) PROCEDURE TRAY, Kit SKU DYNDA2966A; 5) PROCEDURE TRAY, Kit SKU DYNDA2966A; 6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C; 7) PORT DRESSING KIT, Kit S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1346-2026·2026-02-18

    Azurion 7 B12 systems recalled over tables that may move unexpectedly

    Philips is recalling 655 units of the Azurion 7 B12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0334-2026·2026-02-18

    Ketamine injection bags recalled over a lack of assurance of sterility

    Fresenius Kabi Compounding is recalling 1,410 bags of Ketamine HCl injection over a lack of assurance of sterility.

    Product
    ketamine HCl, 1,000 mg, 1,000 mg per 100 mL (10 mg per mL) in Sodium Chloride Injection, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-050-56
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0509-2026·2026-02-18

    Panjiri recalled because milk is undeclared in the ingredient statement

    Karison Foods & Snacks is recalling 230 cases of Karison brand Panjiri, 12 oz, because the product contains milk which is undeclared in the ingredient statement.

    Product
    Karison brand PANJIRI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Almonds, Sugar, Lotus Seeds, Fennel Seeds, Flax Seeds, Edible Gum, Ginger Powder, Zero Trans Fat Vegetable Shortening; UPC: 8 97307 00243 7; Distributed By: Karison Foods & Snacks Inc.; 34 Willowdale Ave., P
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1347-2026·2026-02-18

    Azurion 7 B20 systems recalled over tables that may move unexpectedly

    Philips is recalling 1 of the Azurion 7 B20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0317-2026·2026-02-18

    Testosterone 18mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 146 pellets of Testosterone, 18.0 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 18.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1018-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1348-2026·2026-02-18

    Azurion 7 M12 systems recalled over tables that may move unexpectedly

    Philips is recalling 1 of the Azurion 7 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1314-2026·2026-02-18

    Breast biopsy needles recalled over particulates that can enter tissue

    Hologic is recalling 681,870 Brevera Breast Biopsy System disposable 9 gauge needles because particulates in affected devices can be deposited into breast tissue during use.

    Product
    Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0311-2026·2026-02-18

    Estradiol 18mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 1,699 pellets of ESTRADIOL, 18 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 18 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 3521, NDC: 79559-3018-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1329-2026·2026-02-18

    Port and line access kits recalled over open swabstick applicator seals

    Medline is recalling 7,570 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT, Kit SKU DT22710; 2) LINE KIT, Kit SKU DYNDA1857A; 3) PICC REMOVAL KIT, Kit SKU DYNDC1978A; 4) PORT ACCESS TRAY, Kit SKU DYNDC2367; 5) NICU CENTRAL LINE TRAY, Kit SKU DYNDC2407B; 6) CVC DRESSING
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0336-2026·2026-02-18

    Vancomycin injection bags recalled over a lack of assurance of sterility

    Fresenius Kabi Compounding is recalling 1,578 bags of Vancomycin HCl injection over a lack of assurance of sterility.

    Product
    vancomycin HCl, 1.5 grams, 1.5 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-016-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1318-2026·2026-02-18

    Spectral CT 7500 scanners recalled over rotor fasteners that may loosen

    Philips is recalling 3 units of the Spectral CT 7500 on Rails because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.

    Product
    Spectral CT 7500 on Rails; Product Code (REF): 728334;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0493-2026·2026-02-18

    Sonic Tots recalled over small hard plastic fragments in product

    McCain Foods USA is recalling 67 cases of Sonic Tots frozen potato product over foreign material described as small hard plastic fragments.

    Product
    Sonic Tots, item number SON00543. Frozen potato product is packaged in clear unlabeled poly bags (6/5 lb), Net Wt 30 lbs (13.61 kg)/ case. UPC 0 00 72714 00543 5. Manufactured By: McCain Foods USA Inc. Oakbrook Terrace, IL.
    Category
    Food
    Distribution
    28 states
  • HighFDA (Devices)·Z-1351-2026·2026-02-18

    Azurion 5 M20 systems recalled over tables that may move unexpectedly

    Philips is recalling 922 units of the Azurion 5 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1340-2026·2026-02-18

    GammaPlan software recalled over plans that may irradiate the wrong location

    Elekta is recalling Leksell GammaPlan versions 11.3 and 11.4 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.

    Product
    Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11,3, 11.4 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1334-2026·2026-02-18

    Dressing change trays recalled over open swabstick applicator seals

    Medline is recalling 8,445 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C; 2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A; 3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615; 4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660; 5) CENTRAL LINE DRESS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1349-2026·2026-02-18

    Azurion 7 M20 systems recalled over tables that may move unexpectedly

    Philips is recalling 5 of the Azurion 7 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1339-2026·2026-02-18

    GammaPlan 11.1 recalled over plans that may irradiate the wrong location

    Elekta is recalling Leksell GammaPlan version 11.1 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.

    Product
    Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1345-2026·2026-02-18

    Azurion 3 M15 systems recalled over tables that may move unexpectedly

    Philips is recalling 802 units of the Azurion 3 M15 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0316-2026·2026-02-18

    Testosterone 12.5mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 3,871 pellets of Testosterone, 12.5 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 12.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1012-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0325-2026·2026-02-18

    Testosterone 303mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 1,015 pellets of Testosterone, 303 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 303 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1303-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0313-2026·2026-02-18

    Estradiol 22mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 133 pellets of ESTRADIOL, 22 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 22 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3022-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0520-2026·2026-02-18

    Aonic Complete Hers shots recalled over possible coliforms and E. coli

    TKS Co-pack Manufacturing is recalling 3,630 bottles of Aonic Complete Hers liquid dietary supplement over possible coliforms, E. coli and Pseudomonas aeruginosa contamination.

    Product
    Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, induction sealed closed with plastic lid. Each bottle is a serving intended to be taken orally as a dietary supplement. Shipping unit: two 15 count decorated box
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0328-2026·2026-02-18

    Testosterone 100mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 4,599 pellets of Testosterone 100mg, Triamcinolone Acetonide 20mcg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone 100mg, Triamcinolone Acetonide 20mcg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC:79559-6100-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0495-2026·2026-02-18

    Spicy breakfast burritos recalled over small hard plastic fragments

    MG Foods-Compass Group is recalling 3,099 Spicy Breakfast Burritos, 10 oz, over foreign material described as small hard plastic fragments.

    Product
    Spicy Breakfast Burrito in a flour tortilla. Net Weight 10 oz (283g) Scrambled eggs, Salsa, Potatoes, Jalapenos, Cheddar, Green Pepper & Onion. UPC 1 00001-00029 7. Keep Refrigerated. Manufactured By: MG Foods, Oak Creek, WI 53154.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Drugs)·D-0337-2026·2026-02-18

    Vancomycin 2 gram bags recalled over a lack of assurance of sterility

    Fresenius Kabi Compounding is recalling vancomycin HCl 2 grams in 500 mL sodium chloride injection over a lack of assurance of sterility.

    Product
    vancomycin HCl, 2 grams, 2 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-019-59.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0318-2026·2026-02-18

    Testosterone 25mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 89,074 pellets of Testosterone, 25.0 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 25.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1025-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0507-2026·2026-02-18

    No sugar besan laddoo recalled because milk is undeclared in ingredients

    Karison Foods & Snacks is recalling 230 cases of Karison brand No Sugar Added Besan Laddoo because the product contains milk which is undeclared in the ingredient statement.

    Product
    Karison brand NO SUGAR ADDED BESAN LADDOO; Ingredients: Gram Flour, Butter, Zero Trans Fat Vegetable Shortening (Hydrogenated Soybean Oil), Pistachio, Almonds, Sweetener with Nutrasweet; UPC: 8 97397 00221 5; Distributed By: Karison Foods & Snacks, Inc, 34 Willowdale Ave., Port W
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0331-2026·2026-02-18

    Testosterone and anastrozole pellets recalled over potential metal particulate

    Asteria Health is recalling 1,464 pellets of Testosterone 100mg, Anastrozole 4mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone 100mg Anastrozole 4mg , 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V094000·2026-02-18

    2025 Lexus LX vehicles recalled for transmission control software defect

    Toyota is recalling certain 2025-2026 Lexus LX600 vehicles due to a potential transmission solenoid failure that can damage the transmission, causing loss of drive power or fluid leaks that increase crash and fire risk.

    Product
    LEXUS — LEXUS LX, LS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0502-2026·2026-02-18

    Peanut butter cups recalled over blue plastic found in a filter

    Ventura Foods is recalling 17 after the firm found pieces of blue plastic in a filter during production.

    Product
    CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018; PEANUT BUTTER NET WT. 0.5OZ & NET WT 0.75OZ DIST BY: DYMA BRANDS, INC. ATLANTA, GA 30328; Product also sold under the following brand names: FLAVOR Fresh PEANUT BUTTER NET WT 0.75 OZ(21g) DISTR
    Category
    Food
    Distribution
    40 states

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