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

2751–2775 of 36527

SevereFDA (Drugs)·D-0299-2025·2025-04-02
SinuCleanse Nasal Wash System Recalled for Bacterial Contamination
Ascent Consumer Products Inc. is recalling SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System nationwide due to bacterial contamination with Staphylococcus aureus. Affected lot number is 024122661Al with expiration date 12/2027.
Product
SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 Soft tip Squeeze Bottle, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1390-2025·2025-04-02
Shiley Adult Tracheostomy Tubes Recalled Due to Flange Disconnection Risk
Covidien is recalling 780 Shiley Adult Flexible Tracheostomy Tubes because the flange may disconnect from the outer cannula, potentially causing respiratory failure, aspiration, or death.
Product
Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula, REF: 7CN80R
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1396-2025·2025-04-02
CVAC Aspiration System Requires Labeling Update for Pressure Risk
The CVAC Aspiration System requires a labeling update to add safety instructions for high-viscosity kidney fluid. Continuing fluid inflow without adequate outflow can create dangerous intrarenal pressure imbalances.
Product
CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of urinary tract and kidney interior.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0300-2025·2025-04-02
SinuCleanse Nasal Saline Packets Recalled for Bacterial Contamination
SinuCleanse Premixed Saline Packets sold nationwide are being recalled due to contamination with Staphylococcus aureus, a bacterium that can cause infection.
Product
SinuCleanse Premixed SALINE PACKETS (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg) for Nasal Wash System, 60-count All Natural USP Grade Saline Packets, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00103 4
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25V203000·2025-04-01
Gillig Recalls 2023-2024 Low Floor Buses Due to Battery Fire Risk
Gillig is recalling 2023-2024 Low Floor transit buses because loose battery hardware may cause short circuits, increasing the risk of fire or loss of drive power.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V204000·2025-04-01
Bollinger Motors Recalls 2025 B4 Trucks Due to Battery Seal Defect
Bollinger Motors is recalling 2025 B4 trucks because the high-voltage battery pack may be improperly sealed, allowing liquid entry that could cause fire, shock, or loss of drive power.
Product
BOLLINGER MOTORS — BOLLINGER MOTORS B4
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25E022000·2025-03-31
Our Next Energy Recalls Aries LFP Battery Packs for Commercial Trucks
Our Next Energy is recalling Aries LFP battery packs for commercial trucks because improper sealing may allow liquid entry, increasing the risk of fire or shock.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V198000·2025-03-28
Ford 3.5L engines can leak oil rapidly from misaligned cup plug
Ford is recalling certain 2024-2025 F-150, Expedition and 2024 Lincoln Navigator vehicles with 3.5L GTDI engines because a misaligned engine cup plug can cause a rapid oil leak.
Product
FORD — FORD, LINCOLN EXPEDITION, F-150, NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V199000·2025-03-28
Ford Recalls 2025 F-150 Hybrid Vehicles Due to Fuse Defect
Ford is recalling 2025 F-150 Hybrid vehicles because an incorrect fuse in the high-voltage battery junction box may fail, causing a sudden loss of drive power.
Product
FORD — FORD F-150 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V200000·2025-03-28
Great Dane Recalls 2025-2026 Champion Trailers Due to Tire Defect
Great Dane is recalling 2025-2026 Champion Dry Van trailers equipped with specific Bridgestone tires that may fail due to incorrect manufacturing.
Product
GREAT DANE — GREAT DANE CHAMPION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V196000·2025-03-28
Ford Recalls 2019-2020 Transit Connect for Engine Overheating Risk
Ford is recalling 2019-2020 Transit Connect vehicles to update software that may delay engine cooling, increasing the risk of a fire.
Product
FORD — FORD TRANSIT CONNECT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V195000·2025-03-27
Honda ADV160 scooter oil pump gear can fail losing drive power
Honda is recalling certain 2024-2025 ADV160 scooters because the oil pump driven gear may fail, resulting in a loss of drive power.
Product
HONDA — HONDA ADV160
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V191000·2025-03-27
Chrysler Recalls 2025 Pacifica Plug-In Hybrids for Brake Caliper Bolt Issue
Chrysler is recalling 2025 Pacifica Plug-In Hybrids because improperly tightened front brake caliper bolts may cause brake failure and reduced steering control.
Product
CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1284-2025·2025-03-26
Smiths Medical ProPort Venous Access System Recalled for Port Separation Risk
Smiths Medical is recalling ProPort Plastic Venous Access Systems due to a manufacturing defect that can cause the port housing and reservoir to separate. This may result in device failure affecting patients worldwide.
Product
smiths medical ProPort Plastic Venous Access System, Pre-assembled with PolyFlow Polyurethane Catheter, 2.6mm O.D. (7.8Fr) x 1.6mm I.D., REF 21-4172-24
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1277-2025·2025-03-26
Smiths Medical ProPort Plastic Venous Access System Recalled
Smiths Medical is recalling the ProPort Plastic Venous Access System due to a manufacturing defect that may cause the plastic port housing and reservoir to separate.
Product
smiths medical ProPort Plastic Venous Access System, Silicone Catheter, 2.87,,O.D. (8.4Fr) s 1.0mm I.D., REF 21-4150-24
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1285-2025·2025-03-26
Smiths Medical ProPort Plastic Venous Access System Recalled for Port Housing Separation Risk
Smiths Medical is recalling certain ProPort Plastic Venous Access System devices due to a manufacturing defect that may cause the port housing and reservoir to separate.
Product
smiths medical ProPort Plastic Venous Access System, Pre-assembled with PolyFlow Polyurethane Catheter, 2.6mm (7.8Fr) O.D. x 1.6mm I.D., 8.5Fr Introducer, REF 21-4173-24
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1280-2025·2025-03-26
Smiths Medical ProPort Implantable Port Housing May Separate Due to Manufacturing Defect
Smiths Medical is recalling 9,506 ProPort implantable venous access ports due to a manufacturing defect that may cause the port housing and reservoir to separate. No injuries have been reported.
Product
smiths medical ProPort Plastic Venous Access System, PolyFlow Polyurethane Catheter, 1.9mm (5.8Fr) O.D. x 1.0mm I.D., 6Fr Introducer, REF 21-4153-24
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1288-2025·2025-03-26
Smiths Medical ProPort Implantable Port Plastic Housing May Separate
The ProPort Low Profile Plastic Venous Access System is being recalled because the port housing and port reservoir may separate due to a manufacturing defect, affecting approximately 2,236 units distributed worldwide.
Product
smiths medical ProPort Low Profile Plastic Venous Access System, Silicone Catheter, 2.8mm (8.4Fr) O.D. x 1.0mm I.D., 9Fr Introducer, REF 21-4187-24
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1278-2025·2025-03-26
Smiths Medical ProPort Implantable Venous Ports Recalled for Separation Defect
Smiths Medical has recalled 643 ProPort Plastic implantable venous access ports that may separate due to a manufacturing defect. The recall affects units distributed worldwide.
Product
smiths medical ProPort Plastic Venous Access System, Silicone Catheter, 2.8mm (8.4Fr) O.D. x 1.0mm I.D., 9 Fr Introducer, REF 21-4151-24
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1287-2025·2025-03-26
Smiths Medical ProPort Venous Ports Recalled for Potential Housing Separation
Smiths Medical is recalling ProPort Low Profile Plastic Venous Access Systems because the plastic port housing and reservoir may separate due to a manufacturing defect. Approximately 8,515 units worldwide are affected.
Product
smiths medical ProPort Low Profile Plastic Venous Access System, PolyFlow Polyurethane Catheter, 1.9mm (5.8Fr) O.D. x 1.0mm., 6Fr Introducer, REF 21-4183-24
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1282-2025·2025-03-26
Smiths Medical ProPort Plastic Venous Access System recalled for port separation defect
Smiths Medical is recalling its ProPort Plastic Venous Access System due to a manufacturing defect that may cause the plastic port housing and reservoir to separate, affecting 1,695 units distributed worldwide.
Product
smiths medical ProPort Plastic Venous Access System, Pre-assembled with PolyFlow Polyurethane Catheter, 2.6mm (7.8Fr) O.D. x 1.6mm I.D., 8.6Fr Introducer, REF 21-4165-24
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1283-2025·2025-03-26
Smiths Medical ProPort Plastic Implantable Ports Recalled for Port Housing Separation
Smiths Medical is recalling 1961 units of ProPort Plastic Implantable Ports worldwide due to a manufacturing defect that may cause the port housing and reservoir to separate. This Class I recall affects patients dependent on venous access systems.
Product
smiths medical ProPort Plastic Venous Access System, PolyFlow Catheter, 2.6 (7.8Fr) O.D. x 1.6mm I.D., 8.5Fr Introducer, REF 21-4171-24
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-0646-2025·2025-03-26
Enoki Mushrooms Recalled Due to Listeria Monocytogenes Contamination
Daily Veggies Enoki Mushroom from New Age International is being recalled because of Listeria monocytogenes contamination. Consumers who purchased this product should not consume it.
Product
Daily Veggies Enoki Mushroom; Product of Korea; Net WT. 200 g (7.05 oz); KEEP REFRIGERATED; Cook through before
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0657-2025·2025-03-26
Strawberry Nutritional Shake Recalled Due to Listeria Contamination Risk
Lyons Magnus is recalling Ready Care and Imperial brand Strawberry Shakes (No Sugar Added) due to potential Listeria monocytogenes contamination. The affected products were distributed to healthcare facilities nationwide.
Product
Ready Care Strawberry Shake No Sugar Added (4 oz), UPC 10045796017372; Imperial Strawberry Shake No Sugar Added (4 oz), UPC 00074865926843
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1286-2025·2025-03-26
Smiths Medical ProPort Implantable Port May Separate Due to Manufacturing Defect
Smiths Medical is recalling ProPort Plastic Venous Access Ports because the port housing and reservoir may separate due to a manufacturing defect. Contact your physician if you have an affected device.
Product
smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems, 82-24
Category
Medical Device
Distribution
0 states

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