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

9801–9825 of 31231

ModerateFDA (Devices)·Z-0652-2025·2024-12-18
ICU Medical ChemoLock Closed System Transfer Device Packaging Recall
ICU Medical is recalling 6,000 units of ChemoLock Close Vial Spike (Model CL-80) due to incorrect packaging and labeling of finished goods. Units were distributed in Illinois and Canada.
Product
ChemoLock Close Vial Spike REF CL-80 The Chemolock Closed System Transfer Device prevents the transfer of environmental contaminants. The Chemolock is needle free and cannot be deactivated, which will passively aid in preventing needlestick injuries and the exposure to cytoto
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0113-2025·2024-12-18
Varithena Administration Pack Recalled Due to Incorrect Syringe Connector Type
Biocompatibles is recalling 432 Varithena (polidocanol injectable foam) Administration Packs due to incorrect syringe connectors. The packs contain luer lock syringes instead of the required luer slip connection syringes.
Product
Varithena (polidocanol injectable foam) Administration Pack, Contains: 3 silicone-free syringes, 2 compression pads, 1 Varithena Transfer Unit, 1 manometer tubing, Rx Only, Distributed by Biocompatibles Inc., a BTG International Group company. CN01114.3
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0669-2025·2024-12-18
Hologic Sizer Set Missing Instructions for Use and Sterilization
Hologic is recalling 178 units of Sizer Set surgical instruments nationwide because instructions for use and revised sterilization instructions were not provided with the product.
Product
Hologic Sizer Set- sterilization tray and 6 individual sizers, intended as a Surgical instrument guide Model/Catalog Number: F0101
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·25066·2024-12-12
HTRC C240 Battery Chargers Recalled for Fire and Burn Hazards
HTRC C240 battery chargers may ignite or cause connected batteries to ignite, posing fire and burn hazards. The recall affects about 34,600 units sold online from December 2017 through June 2024.
Product
HTRC C240 battery chargers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25063·2024-12-12
Stanley Recalls 2.6 Million Travel Mugs for Burn Hazard
Stanley is recalling 2.6 million Switchback and Trigger Action travel mugs whose lids can detach during use, causing burn injuries. The company has received 91 reports worldwide (16 in the U.S.) of lid detachment resulting in 38 burn injuries, with 11 requiring medical attention.
Product
Switchback and Trigger Action travel mugs
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·24V926000·2024-12-12
2024 Jeep Grand Cherokee Radiator Crossmember Bolts May Not Be Properly Secured
Chrysler is recalling 631 units of the 2024 Jeep Grand Cherokee and Grand Cherokee L due to unsecured radiator crossmember bolts that may cause improper airbag deployment and fuel leaks during crashes, increasing injury and fire risks.
Product
JEEP — 2024 JEEP GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25067·2024-12-12
Wireless Tree Light Controllers Recalled Due to Fire Hazard
Wireless tree light controllers sold at Walmart, Target, and Cracker Barrel are being recalled because the receiver can overheat and catch fire. Ten overheating incidents and one fire have been reported, with no injuries.
Product
Wireless Decorative Tree Light Controllers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V925000·2024-12-12
2025 Chevrolet Equinox EV Pedestrian Alert Sound System Defect
General Motors is recalling 7,606 2025 Chevrolet Equinox EV vehicles due to incorrect pedestrian alert sound software that fails to produce sufficient volume. This violates federal safety standards and may increase the risk of pedestrian injury.
Product
CHEVROLET — 2025 CHEVROLET EQUINOX EV
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25065·2024-12-12
Yoto Mini speakers recalled for battery fire and burn hazards
Yoto Inc. is recalling approximately 251,165 Yoto Mini speakers because the lithium-ion battery can overheat and catch fire. No injuries have been reported, but consumers should stop using the product and contact Yoto for a free battery replacement kit.
Product
Yoto Mini speakers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25064·2024-12-12
Wall Teester Bed Crowns Recalled Due to Mounting Tab Failure
Touch of Class is recalling about 890 Wall Teester Bed Crowns because their welded mounting tabs can weaken and fail, causing the crown to fall from the wall. One injury has been reported.
Product
Wall Teester Bed Crowns
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0248-2025·2024-12-11
Albertsons Ready-Meal Salads Recalled for Listeria Contamination
Albertsons Companies LLC recalls multiple ready-meal salad products due to Listeria monocytogenes contamination in cooked chicken. Products were distributed across 21 US states with sell-through dates through October 13, 2024.
Product
(1) GINGER CHICKEN BROCCOLI SALAD FS (UPC 27110800000) (2) READY MEALS GINGER CHICKEN BROCOLLI SALAD SS (UPC 29105700000) (3) GINGER BROCOLLI SALAD FS (UPC 29233600000) (4) CHICKEN CAESAR SALAD FS (UPC 29130700000) (5) CAESAR CHICKEN BOWL (UPC 29125500000) (6) READY MEALS CHICKEN
Category
Food
Distribution
21 states
SevereFDA (Drugs)·D-0083-2025·2024-12-11
VitalityXtra Capsules Recalled for Undeclared Sildenafil and Diclofenac
VitalityXtra Capsules containing undeclared sildenafil and diclofenac are being recalled nationwide. The product was marketed without required FDA approval and poses health risks from undeclared pharmaceutical ingredients.
Product
VitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtra, San Francisco, CA www.vitalityxtra.com
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0086-2025·2024-12-11
ZapMax Capsules Recalled for Undeclared Sildenafil and Diclofenac
ZapMax Capsules, 500 mg are recalled for containing undeclared sildenafil and diclofenac without FDA approval. The product was distributed nationwide; consumers should stop using immediately and consult their healthcare provider.
Product
ZapMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZapMax, 2108 N St. Sacramento, CA 95816, www.zapmax.com
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0084-2025·2024-12-11
PeakMax Capsules Recalled for Undeclared Sildenafil and Diclofenac
PeakMax Capsules contain undeclared sildenafil and diclofenac and were marketed without FDA approval. This Class I recall affects capsules distributed nationwide.
Product
PeakMax Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: PeakMax, San Francisco, CA, www.PeakMax.com
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0085-2025·2024-12-11
ZoomMax Capsules contain undeclared sildenafil and diclofenac
ZoomMax Capsules have been recalled by the FDA due to containing undeclared sildenafil and diclofenac. The product was marketed without FDA approval.
Product
ZoomMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZoomMax, 2108 N St. Sacramento, CA 95816, www.zoommax.com
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0257-2025·2024-12-11
Fresh Express Salad Bowls Recalled for Potential Listeria Contamination
Fresh Express Gourmet Cafe Santa Fe Greek salad bowls are being recalled due to potential Listeria monocytogenes contamination linked to a chicken ingredient recall. No illnesses have been reported.
Product
Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279 40713 5 and Case Code :71279-56704
Category
Food
Distribution
12 states
SevereFDA (Food)·F-0256-2025·2024-12-11
Fresh Express Chicken Caesar Salad Bowls Recalled for Listeria Monocytogenes
Fresh Express Gourmet Cafe Chicken Caesar salad bowls are being recalled due to potential Listeria monocytogenes contamination linked to a Bruce Pac recall. The recall affects products distributed across multiple U.S. states.
Product
Fresh Express Gourmet Cafe Chicken Caesar 5.75oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279407074 and Case Code:071279565620
Category
Food
Distribution
12 states
SevereFDA (Food)·F-0245-2025·2024-12-11
Wegmans Asian Sesame Salad recalled for undeclared egg
Wegmans Large Asian Sesame Salad with Chicken contains undeclared egg, a common allergen. The recall affects 365 units distributed across nine states.
Product
Wegmans Large Asian Sesame Salad with Chicken and Asian Peanut Dressing.
Category
Food
Distribution
9 states
SevereFDA (Food)·F-0255-2025·2024-12-11
Enoki Mushrooms Recalled for Potential Listeria Contamination
HH Fresh Trading is recalling enoki mushrooms distributed to West Virginia retail stores due to potential Listeria monocytogenes contamination. Consumers should not consume this product.
Product
ENOKI MUSHROOM; 200g/package (25 packages/case); vacuum packed; refrigerated "***ENOKI MUSHROOM***Net WT***200g(1.05oz)***To keep sealed & cold Product of Taiwan Distributed by: HH Fresh Trading Los Angeles CA 90063 Exported by JIA YANG INTERNATIONAL ENTERPRISES CO., LTD. Produc
Category
Food
Distribution
0 states
HighFDA (Food)·F-0235-2025·2024-12-11
Vanilla Pudding Mix Recalled Due to Metal Fragment Contamination
Sysco Classic Vanilla Instant Pudding & Pie Filling Mix is recalled for metal fragments found in the product due to a damaged sifter used during dextrose production.
Product
Sysco Classic Vanilla Instant Pudding & Pie Filling Mix Natural and Artificial Flavor, NET WT. 32 OZ (2 LB) 907g, UPC 0 74865 20116 2, Case UPC 10074865201169, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077
Category
Food
Distribution
30 states
HighFDA (Drugs)·D-0109-2025·2024-12-11
Cinacalcet Tablets Recalled for Elevated Nitrosamine Impurity
AvKARE is recalling 2,396 bottles of Cinacalcet Tablets 60 mg (Lot #44550) distributed nationwide due to CGMP deviations. The tablets contain N-Nitroso-Cinacalcet, a nitrosamine impurity, above acceptable intake limits.
Product
Cinacalcet Tablets, 60 mg, 30-count bottle, Rx only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 42291-460-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0639-2025·2024-12-11
Medline Convenience Kits Recalled Due to Defective Smoke Evacuation Component
Medline is recalling L&D convenience kits distributed nationwide because they were manufactured with smoke evacuation pencils that Stryker subsequently recalled. The affected kits contain components from lot 23HMI048.
Product
MEDLINE convenience kits labeled as: L&D MINOR PACK, REF DYNJ82672
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0228-2025·2024-12-11
REJUV ORIGINALS Orange Drink Mix Recalled for Metal Fragments
DYMA BRANDS is recalling REJUV ORIGINALS Low Calorie Orange Drink Mix due to metal fragments introduced during production. The contaminated product was distributed across 29 states.
Product
REJUV ORIGINALS LOW CALORIE ORANGE DRINK MIX NATURAL FLAVOR, NET WT. 8.6 OZ. (244g), UPC 8 22486 14388 6, Case UPC 30822486143887, MARKETED BY INDEPENDENT MARKETING ALLIANCE HOUSTON, TX 77043
Category
Food
Distribution
30 states
HighFDA (Devices)·Z-0579-2025·2024-12-11
Ziehm Vision RFD 3D Hand Switch Defect May Cause Unintended Radiation
The Ziehm Vision RFD 3D hand switch can fail when exposed to mechanical stress like dropping, potentially initiating unintended radiation from the x-ray system.
Product
Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0222-2025·2024-12-11
AROMA VITA Hot Cocoa Mix Recalled for Metal Fragments
AROMA VITA Hot Cocoa Mix is being recalled due to metal fragments in the product caused by a damaged sifter used during dextrose production.
Product
AROMA VITA HOT COCOA MIX, NET WT. 32OZ (2LBS) 907g, UPC 7 1908 50007 0, Case UPC 50719098500075, Distributed by DYMA Brands, Inc. Atlanta, GA 30328
Category
Food
Distribution
30 states

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9801–9825 of 31231