Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

3926–3950 of 113838

HighFDA (Devices)·Z-1419-2026·2026-02-25
Robotic surgery kits recalled over sterilization equipment calibration issues
Medline is recalling 7,725 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) BAP NORTH ROBOTIC SURGERY CDS, Model Number: CDS982407N; 2) TOT/ GYN LITHOTOMY CDS, Model Number: CDS985431K; 3) TOT/ GYN LITHOTOMY CDS, Model Number: CDS985431O; 4) KIT ROBOTICS GYN, Model Number: DYKMBNDL109A; 5) KIT ROBOTICS UROLOGY PROSTA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1363-2026·2026-02-25
MediHoney wound gel recalled over potential packaging failures
Integra LifeSciences is recalling 49,367 units of MediHoney Gel with Active Leptospermum Honey over potential packaging failures that could breach the sterile barrier.
Product
MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with Active Leptospermum Honey provides a moist environment conducive to wound healing and is indicated for light to moderately exuding wounds.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1377-2026·2026-02-25
Thunderbeat pistol grip devices removed after continued adverse event reports
Olympus is removing the Olympus Thunderbeat, 5 mm, 45 cm, Pistol Grip from the market, stating the action is due to continued reports of adverse events.
Product
Olympus Thunderbeat, 5 mm, 45 cm, Pistol Grip
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1413-2026·2026-02-25
Medline Convenience Kits Recalled Due to Potential Sterility Assurance Issues
Medline Industries, LP is recalling various Medline Convenience Kits because equipment calibration issues may have impacted the sterility assurance level of the products.
Product
Medline Convenience Kits: 1) NEURO SHUNT- CODMAN, Model Number: CDS860018G; 2) NEURO SHUNT- CODMAN, Model Number: CDS860018I; 3) KIT NEUR FUS LUM POST CRANDALL, Model Number: DYKMBNDL138; 4) KIT NEURO FUS LUM POST SANSUR, Model Number: DYKMBNDL142; 5) KIT NEURO FUS LUM P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1379-2026·2026-02-25
Olympus Thunderbeat Grip Medical Device Recall for Adverse Events
Olympus Corporation is recalling 30 Thunderbeat 5 mm, 45 cm Inline Grips due to continued reports of adverse events during medical procedures.
Product
Olympus Thunderbeat, 5 mm, 45 cm Inline Grip
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1391-2026·2026-02-25
PICC line and code cart kits recalled over sterilization calibration issues
Medline is recalling 5,346 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) PICC LINE TRAY, Model Number: 00-401993O; 2) CODE CART ADULT 4 CENTRAL LINE, Model Number: ACC010268B; 3) CODE CART ADULT 4 CENTRAL LINE, Model Number: ACC010268C; 4) TRAY 6 CENTRAL LINE A, Model Number: ACC010487; 5) PEDS PICC INSERTION TRAY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1422-2026·2026-02-25
Arthroscopy kits recalled over sterilization equipment calibration issues
Medline is recalling 175 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) ARTHROSCOPY CDS, Model Number: CDS984609B; 2) ARTHROSCOPY TRAYS, Model Number: DYNJ22501G; 3) ARTHROSCOPY PACK, Model Number: DYNJ32715F; 4) CHS ARTHROSCOPY PACK, Model Number: DYNJ50834C; 5) ARTHROSCOPY TRAY-LF, Model Number: DYNJ51069
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1423-2026·2026-02-25
Surgical drapes recalled over sterilization equipment calibration issues
Medline is recalling 14,927,765 units of surgical drapes because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Product
Medline Surgical Drapes: 1) SHEET,DRAPE,40X58,STERILE, Model Number: DYNJP2410; 2) DRAPE,SHEET,ECONOMY,40X58",ST,20/CS, Model Number: DYNJP2411; 3) SHEET,DRAPE, 40X70,STERILE, Model Number: DYNJP2412; 4) DRAPE,MEDIUM,TAPE,40X70",ST,50/CS, Model Number: DYNJP2412T; 5) SHE
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-1427-2026·2026-02-25
Stryker MOLLI 2 System Recall: Marker Dislodgement Risk
Stryker is recalling the MOLLI 2 System due to magnetized surgical tools that may dislodge markers during target tissue removal procedures. The recall affects 5,864 units distributed worldwide.
Product
MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195028 MS-00009 (Pack of 10) - MOLLI Introducer (12cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195134 MP2001 - MOLLI 2 Wand UDI (GTIN): 008500241951
Category
Medical Device
Distribution
Distributed nationwide
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-1370-2026·2026-02-25
Capillary tubes recalled over a positive bias in potassium results
Medica Corporation is recalling 1,578 capillary tube kits after a systematic positive bias of up to 20% was identified across the reportable potassium range.
Product
Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit.
Category
Medical Device
Distribution
0 states
ModerateFDA (Food)·H-0513-2026·2026-02-25
Aluminum Kadai with Metal Handles Recalled Due to Potential Lead Contamination
Lotus Mom Corporation is recalling Aluminum Kadai with Metal Handles (Size 5) due to the potential for lead leaching.
Product
Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN INDIA SIZE 5 Sticker label: $$24.99+TX
Category
Consumer Product
Distribution
2 states
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
HighCPSC·26287·2026-02-24
Magnetic chess games recalled over loose magnets that can be swallowed
About 5,300 Christmas-themed magnetic chess games are being recalled because they contain loose magnets posing an ingestion hazard to children.
Product
Christmas-themed Magnetic Chess Games
Category
Consumer Product
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·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
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·26V101000·2026-02-20
Ford Recalls 2017-2019 Explorers for Rear Suspension Toe Link Fracture Risk
Ford is recalling 2017-2019 Explorers because rear suspension toe links may fracture, potentially causing loss of steering control and increasing crash risk.
Product
FORD — FORD EXPLORER
Category
Vehicle
Distribution
Distributed nationwide

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3926–3950 of 113838