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

23151–23175 of 26062

HighFDA (Food)·F-0399-2022·2022-01-19
Raw Vegan Protein Peanut Butter Recalled for Undeclared Coconut
NutraCap Labs LLC is recalling Raw Vegan Protein Peanut Butter dietary supplement because it contains undeclared coconut, which poses a risk to consumers with coconut allergies.
Product
RAW VEGAN PROTEIN PEANUT BUTTER NET WEIGHT 2.04LBS (925 GRAMS) DIETARY SUPPLEMENT Other Ingredients: Pea Protein Isolate, Brown Rice Protein, ***Sunflower (Non-Dairy) Creamer, Salt, Steviol Glycoside (95%) Manufactured in the U.S.A. for RAW, 838 SW Federal Highway, Stuart, Florid
Category
Food
Distribution
26 states
HighFDA (Food)·F-0419-2022·2022-01-19
BlakeFit Everyday All-in-one Lime Watermelon Recalled for Undeclared Milk
NutraCap Labs LLC is recalling BlakeFit Everyday All-in-one Lime Watermelon 44oz jars because the product contains undeclared milk, which poses a risk to consumers with milk allergies.
Product
BlakeFit Everyday All-in-one Lime Watermelon 44oz Jar UPC CODE X002J9E9KD 323359000058
Category
Food
Distribution
26 states
HighFDA (Food)·F-0390-2022·2022-01-19
Local Fixe LLC Frozen Dinner Rolls Wheat Allergen Not Declared
Local Fixe LLC is recalling frozen dinner rolls because wheat is not declared on the label, even though flour (which contains wheat) is listed as an ingredient. This poses a serious risk to consumers with wheat allergies.
Product
Dinner Rolls are shaped in rounds and sold frozen. Packaged in clear plastic Ziploc style plastic bags. The weight per package s 1.323 lbs/600 grams. The label is read in parts: "***Dinner rolls ***Flour, sourdough starter, water, egg, sugar, salt, grape seed oil, active dry y
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0488-2022·2022-01-19
Orthopaedic Stem Implants Recalled for Undersized Bore Manufacturing Defect
DePuy Orthopaedics is recalling approximately 870 GLOBAL UNITE STD STEM implants worldwide because an undersized spigot bore may prevent proper separation, causing potential surgical delay or bone damage.
Product
GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0378-2022·2022-01-19
Bosket Bread Jalapeño Cheese Bread Recall: Undeclared Allergens
Bosket Bread Company is recalling Jalapeño Cheese Bread sold in Washington because the packaging lacks an ingredient statement, leaving major allergens (wheat, milk, egg, soy, sesame) undeclared.
Product
Jalape¿o Cheese Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0475-2022·2022-01-19
CT Scanner Software Update Causes Head Image Quality Degradation
Siemens SOMATOM Definition Edge CT scanners with software version VB20_SP5 may produce degraded head images, increasing the risk of patient misdiagnosis. Devices have been distributed nationwide.
Product
SOMATOM Definition Edge -Computed tomography system Model 10590000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0393-2022·2022-01-19
Squid Ink Fettuccine Pasta Recall: Undeclared Wheat Allergen
Local Fixe LLC is recalling Squid Ink Fettuccine fresh pasta because wheat is not declared on the label, despite flour being an ingredient. The product poses a risk to consumers with wheat allergies.
Product
Squid Ink- Fettucine is raw fresh pasta portioned into 4 ounce portions. Each portion is rolled in a wax deli sheet and bulk packaged into a reusable plastic container with varying weight. Each container will have 40-60 portions, net wt. 10-15 lbs (4.536-6.804 kg). The label
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0477-2022·2022-01-19
OCT-Camera Laser Shut-Off Malfunction Poses Patient Safety Risk
Haag-Streit OCT-Camera devices with automatic laser shut-off malfunction may fail to recognize when the laser is safely switched off, posing a potential safety risk.
Product
OCT-Camera 211 01 A1, Running software iOCT-Control 3 v1.4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0381-2022·2022-01-19
Bosket Bread Sourdough Bread Lacks Required Ingredient Statement
Bosket Bread Company is recalling sourdough bread products sold in Washington because packages are missing required ingredient statements, leaving consumers unable to identify potential allergens including wheat, milk, egg, soy, and sesame.
Product
Sourdough Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
Category
Food
Distribution
1 state
HighFDA (Food)·F-0395-2022·2022-01-19
Vemondo Vegan Dessert Cones Recalled for Undeclared Milk Allergen
Lidl US Operations is recalling Vemondo Vegan Caramel & Pannacotta Non-Dairy Dessert Cones because they contain undeclared milk, posing a risk to consumers with milk allergies.
Product
Vemondo Vegan Caramel & Pannacotta Non-Dairy Dessert Cones. 4-3.7 fl oz (110 mL) UPC 4 056489 468653
Category
Food
Distribution
3 states
HighFDA (Food)·F-0389-2022·2022-01-19
Pie Dough Recall: Undeclared Wheat Allergen
Local Fixe LLC is recalling frozen pie dough products because wheat is not declared on the label, even though flour—which contains wheat—is an ingredient. The recall affects 181 packages distributed in Oregon.
Product
Pie Dough are packaged two crusts per pack and sold frozen. They are wrapped in white butcher paper. The weight per package is 1.257 lbs/540 grams. The label is read in parts: "***Pie Dough*** Flour, Butter (cream, milk, salt), Organic Palm Shortening, water, salt ***www.local
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0491-2022·2022-01-19
Medtronic Perfusion Kits Recalled: Missing Endotoxin Testing
Medtronic is recalling approximately 6,653 Custom Perfusion kits used in cardiac procedures because they were labeled as non-pyrogenic without completing required endotoxin testing.
Product
Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM PACK BB10Q85R FILTER (Model BB10Q85R); 2. CUSTOM PACK BB11C01R MIDI DEEP (Model BB11C01R); 3. CUSTOM PACK BB7H95R22 HYP MAIN (Model B7H95R22); 4.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0497-2022·2022-01-19
Vaxxen Labs Norexx Lean Mass Capsules Recalled for Undeclared Milk
NutraCap Labs is recalling Vaxxen Labs Norexx Lean Mass Agent Capsules (90ct bottle, UPC 0 612524 173315, Lot #2109041) because the product contains undeclared milk, which poses a risk to consumers with milk allergies.
Product
Vaxxen Labs Norexx Lean Mass Agent Capsules 90ct Bottle UPC CODE 0 612524 173315
Category
Consumer Product
Distribution
26 states
HighFDA (Food)·F-0391-2022·2022-01-19
Classic Lasagna Pasta Sheets Recalled for Undeclared Wheat Allergen
Local Fixe LLC is recalling Classic Lasagna Pasta sheets because the label declares flour as an ingredient but fails to declare wheat, which is present in the product. Consumers with wheat allergies may face serious health risks.
Product
Classic Lasagna Pasta sheets sold frozen and wrapped in brown freezer paper. The weight per package is 1 lb/453.6 grams. The label is read in parts: "***Classic Lasagna sheets *** Ingredients: Flour, Semolina, Egg, water ***www.localfixe.com***".
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0476-2022·2022-01-19
Philips wireless footswitches for Allura Xper and Azurion X-ray systems recalled for connection issues
Philips wireless footswitches used with Allura Xper and Azurion X-ray systems may experience connection issues that interrupt fluoroscopic imaging during patient procedures. The recall affects 1,971 systems distributed worldwide.
Product
Wireless Footswtich used with the following Philips Allura Xper and Azurion Interventional Fluoroscopic X-ray System . Model Number: 722001, 722002, 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022, 722023, 722024, 722025, 72
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0369-2022·2022-01-19
Bosket Bread Sourdough Dinner Rolls Lack Required Ingredient Labels
Bosket Bread Company is recalling Sourdough Dinner Rolls distributed in Washington because the products lack ingredient statements, leaving consumers unable to identify undeclared wheat, milk, egg, soy, or sesame allergens.
Product
Sourdough Dinner Rolls, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
Category
Food
Distribution
1 state
HighCPSC·22054·2022-01-19
FRIGG Silicone Pacifiers Recalled Due to Choking Hazard
Mushie & Co is recalling about 333,725 FRIGG Silicone Pacifiers because the silicone nipple can detach from the plastic shield, posing a choking hazard. Eight detachments have been reported in the U.S. with no injuries.
Product
FRIGG Silicone Pacifiers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0465-2022·2022-01-19
Subdermal Needle Electrode Corkscrew Recall: Risk of Blue Hub Detachment
Technomed Europe is recalling 117,672 disposable subdermal needle electrodes due to risk of the blue hub detaching, potentially leaving the needle in the patient's scalp.
Product
Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0475-2022·2022-01-19
First Finisher/Ouro Vitae Mito Male Cherry Limeade contains undeclared milk
NutraCap Labs LLC is recalling First Finisher/Ouro Vitae Mito Male Cherry Limeade 16oz jars because they contain undeclared milk, a common allergen.
Product
First Finisher/Ouro Vitae Mito Male Cherry Limeade 16oz Jar NO UPC CODE
Category
Food
Distribution
26 states
HighFDA (Devices)·Z-0495-2022·2022-01-19
LigaSure Blunt Tip Laparoscopic Sealer Devices Recalled for Jaw Opening Defect
Covidien is recalling LigaSure Blunt Tip Laparoscopic Sealer/Divider devices (lot 11320187X) due to an assembly defect that may prevent the device jaws from opening after tissue application, creating a risk of bleeding and tissue injury.
Product
LigaSure Blunt Tip Laparoscopic Sealer/Divider, Nano-Coated, Product Number LF1837
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0371-2022·2022-01-19
Bosket Bread Ciabatta Loaves Recalled for Undeclared Allergens
Bosket Bread Company is recalling Ciabatta Loaves sold in Washington because the packages lack ingredient statements, leaving wheat, milk, egg, soy, and sesame undeclared. Consumers with allergies to these ingredients face a health risk.
Product
Ciabatta Loaves, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
Category
Food
Distribution
1 state
HighFDA (Food)·F-0394-2022·2022-01-19
Vemondo Vegan Coconut & Cocoa Dessert Cones Recall for Undeclared Milk
Lidl US Operations is recalling Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones due to undeclared milk allergen. The product was distributed to retail stores in Maryland, Virginia, and Pennsylvania.
Product
Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl ounces (110 mL) cones UPC 4 056489 468646
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0473-2022·2022-01-19
CT Scanner Software Defect May Degrade Image Quality
Software version VB20_SP5 in certain Siemens CT scanners may degrade head image quality, increasing misdiagnosis risk. The recall affects 794 units distributed nationwide.
Product
SOMATOM Definition AS-Computed tomography system Model 8098027
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0504-2022·2022-01-19
Everything Swapples Recalled for Potential Plastic Contamination
SWAP FOODS LLC is recalling Everything Swapples (11.14 oz) due to an ingredient that may be contaminated with small pieces of plastic. Affected product was distributed to retail stores in Pennsylvania and Wisconsin.
Product
Everything Swapples, Net Wt. 11.14 OZ, UPC 8 64390 00021 3
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0470-2022·2022-01-19
RefleXion Medical Radiotherapy System Recall Due to Dose Discrepancy
Reflexion Medical is recalling three RefleXion X1 radiotherapy systems due to a potential dose discrepancy when delivering treatment in Feet First Supine patient orientation.
Product
RefleXion Medical Radiotherapy System - System Label: "*** refleXion REF RXM1000 ***" Physics Guide/Treatment Delivery User Manual/Treatment Planning User Manual: "RefleXion X1 Model: RXM1000"
Category
Medical Device
Distribution
Distributed nationwide

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23151–23175 of 26062