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

16651–16675 of 27769

HighFDA (Devices)·Z-2416-2023·2023-08-23
Endoscopic Grasper Instrument Recalled for Rotation Knob Failure Risk
Carefusion 2200 Inc is recalling specific lots of the Snowden-Pencer DIAMOND-TOUCH GRASPER endoscopic surgical instrument due to a manufacturing defect that may cause the rotation knob to crack or break, potentially compromising surgical performance.
Product
Snowden-Pencer MIS DIAMOND-TOUCH GRASPER DIAMOND JAW BABCOCK 5MM, 32CM, RATCHETED, REF SP90-7018; endoscopic surgical device
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-1459-2023·2023-08-23
IO Inspired Organics Walnut Halves & Pieces recalled for undeclared walnuts
IO Inspired Organics Walnut Halves & Pieces are recalled because walnuts are not declared in the ingredient and contains statement. The 7oz packages were distributed in 11 states and may pose a risk to consumers with walnut allergies.
Product
IO Inspired Organics brand Organic Raw Walnut Halves & Pieces; 7oz plastic tubs; 9 packages per wholesale case; retail UPC 863669740065, Lipari #943469
Category
Food
Distribution
11 states
HighFDA (Food)·F-1406-2023·2023-08-23
Dilettante Mocha Cafe Truffles recalled for incomplete milk allergen labeling
Dilettante Chocolates Inc is recalling Mocha Cafe brand Light Ephemere Bulk Truffles sold from retail display cases in Washington due to incomplete allergen labeling on the display placard.
Product
Dilettante Mocha Cafe brand Light Ephemere Bulk Truffles, perishable, sold in individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sen
Category
Food
Distribution
1 state
HighFDA (Food)·F-1416-2023·2023-08-23
Dilettante Mocha Cafe Toffee Recalled for Incomplete Allergen Labeling
Dilettante Chocolates recalls Rheingold White Bulk Toffee sold at Washington retail locations due to display placard with incomplete allergen declarations. The placard did not fully identify milk and specific nut allergens present in the product.
Product
Dilettante Mocha Cafe brand Rheingold White Bulk Toffee, perishable, sold individual pieces out of retail display cases. The display placard declares milk, pecans and hazelnuts in the first Contains statement, and the 2nd Contains statement declares "Contains: Dairy, Nuts". Bu
Category
Food
Distribution
1 state
HighFDA (Food)·F-1432-2023·2023-08-23
Garden Cut Romaine Lettuce Recalled for Potential Deer Feces Contamination
Get Fresh Produce is recalling Garden Cut Romaine lettuce (product 9386) because it may be contaminated with deer feces. The recall affects 1,404 pounds distributed in Illinois and Florida.
Product
Garden Cut Romaine 1x1 Chopped 6/2 LB (product number 9386) packed in corrugated boxes with an inner plastic bag (6, 2lb bags per case)
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-2421-2023·2023-08-23
Surgical Clamp Recall: Rotation Knob May Crack or Break
Snowden-Pencer endoscopic surgical clamps may have rotation knobs that crack or break due to manufacturing defect. Lot B23 units should not be used.
Product
Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 50 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7045; endoscopic surgical device
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-1434-2023·2023-08-23
Benton's Snack Packs Recalled for Undeclared Peanut Allergen
Benton's 100 Calorie Snack Packs are recalled because they contain undeclared peanut, a major allergen. Consumers with peanut allergies may experience severe reactions if they consume this product.
Product
Benton's 100 Calorie Snack Packs Baked Chocolate Wafer Snacks 6-0.81 OZ (23g) Packs Net Wt. 4.86 oz UPC: 4 099100 040416 Packaged in a paper carton, 16 cartons per case.
Category
Food
Distribution
7 states
HighFDA (Food)·F-1435-2023·2023-08-23
Annie's Homegrown Graham Snack Recalled for Undeclared Peanut
Annie's Homegrown Gluten Free Bunny Grahams Cocoa & Vanilla 6.75 oz boxes are recalled due to undeclared peanut. Consumers with peanut allergies should not consume this product.
Product
Annie's Homegrown Gluten Free Bunny Grahams Cocoa & Vanilla Flavored With Other Natural Flavors Graham-Style Snacks Net Wt 6.75 oz (191g) UPC: 13562 00019 Packaged in cartons, 7 and 12 retails cartons per case
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-2423-2023·2023-08-23
Surgical grasper recalled for rotation knob cracking due to adhesive defect
Carefusion is recalling Snowden-Pencer endoscopic graspers due to potential rotation knob cracking from a manufacturing adhesive defect. Affected lot B23 was distributed in the US and Canada.
Product
Snowden-Pencer MIS DIAMOND-TOUCH GRASPER CRILE CURVED JAW 5MM, 32CM, RATCHETED, REF SP90-7048; endoscopic surgical device
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-1443-2023·2023-08-23
Brain Enhancer Capsules Recalled for Potential E. coli Contamination
Global Vitality Inc. is recalling Food Research International Serious Brain Enhancer Capsules due to potential E. coli contamination. The product was distributed to a single location in California.
Product
Food Research International - Serious Brain Enhancer Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-2414-2023·2023-08-23
FreeStyle Libre 2 Readers may fail to activate new sensors
FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.
Product
FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2427-2023·2023-08-23
Endoscopic surgical clamp recalled for potential rotation knob failure
Carefusion recalls Snowden-Pencer MIS Diamond-Touch Clamps (Lot B23) due to potential cracking of the rotation knob from incorrect adhesive use. The 7 affected units were distributed to the US and Canada.
Product
Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 25 MM JAW 5MM, 45CM, RATCHETED, REF SP90-7243; endoscopic surgical device
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2405-2023·2023-08-23
Hip Screw Labeled as Wrong Size: 30mm Screws Mislabeled as 25mm
Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.
Product
CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2401-2023·2023-08-23
UroPass Ureteral Access Sheaths Recalled for Dilator Tip Breakage
Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.
Product
UroPass Ureteral Access Sheaths, 5 pieces/box
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2422-2023·2023-08-23
Endoscopic Surgical Clamp Recalled Due to Potential Rotation Knob Failure
Carefusion is recalling specific lots of Snowden-Pencer MIS endoscopic surgical clamps due to potential cracking or breaking of the rotation knob caused by incorrect adhesive use during manufacturing.
Product
Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 60 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7046; endoscopic surgical device
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-1404-2023·2023-08-23
VEROCCA Alfajor Cookies Recalled for Undeclared Wheat, Milk, and Soy Allergens
VEROCCA Locally Handmade Alfajor cookies are being recalled due to undeclared wheat, milk, and soybean oil allergens. Consumers with allergies to these ingredients should not consume the product.
Product
VEROCCA, Locally Handmade, ALFAJOR
Category
Food
Distribution
0 states
HighFDA (Food)·F-1433-2023·2023-08-23
Garden Cut Lettuce Greek Mix Salad recalled for possible deer feces contamination
Get Fresh Produce, Inc. is recalling Garden Cut Lettuce Greek Mix Salad (product number 10149) due to possible contamination with deer feces. Affected product was distributed in Illinois and Florida.
Product
Garden Cut Lettuce Greek Mix Salad (product number 10149) 10 LB packed in corrugated boxes with an inner plastic bag. Product consists of: 1"x1" Romaine, 1/8" red cabbage, and 1/8" green cabbage.
Category
Food
Distribution
0 states
HighFDA (Food)·F-1424-2023·2023-08-23
Lettuce Salad Blend Monterey recalled due to potential deer feces contamination
G.O. Corporation is recalling Lettuce Salad Blend Monterey (Produce Code 404709) from Iowa, Minnesota, North Dakota, and Wisconsin due to potential contamination with deer feces. The recall affects 23,186 pounds across lot codes 130209 and 130212.
Product
Lettuce Salad Blend Monterey, Produce Code 404709, 4-5lb. bags per shipping case.
Category
Food
Distribution
4 states
HighFDA (Food)·F-1405-2023·2023-08-23
Dilettante Dark Ephemere Bulk Truffles Milk Allergen Mislabeling
Dilettante Mocha Cafe Dark Ephemere Bulk Truffles' display placard lists milk in ingredients but declares only 'Contains: Dairy,' not 'Contains: Milk.' Bulk boxes have correct allergen labeling.
Product
Dilettante Mocha Cafe brand Dark Ephemere Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk, cream, and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes
Category
Food
Distribution
1 state
HighFDA (Food)·F-1448-2023·2023-08-23
Frozen Sachertote Recalled for Undeclared Egg, Milk, and Wheat Allergens
Lidl US TRADING is recalling Alpenfest Style Sachertote frozen dessert because egg, milk, and wheat allergens are not declared on the label. Consumers with allergies to these ingredients should not consume the product.
Product
Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-2418-2023·2023-08-23
Endoscopic Dissector Surgical Tool Recalled for Cracking Knob Defect
Carefusion 2200 Inc is recalling Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR endoscopic surgical instruments due to potential cracking of the rotation knob from incorrect adhesive use in manufacturing. Lot B23 is affected.
Product
Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR FENESTRATED 16MM JAW 5MM, 32CM, NON RATCHETED, REF SP90-7036; endoscopic surgical device
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2413-2023·2023-08-23
HF Resection Electrodes Recalled for Wire Breakage and Patient Fragment Hazard
Olympus HF Resection Electrodes are being recalled due to reports of loop wire breakage when contacting metal objects. Broken fragments can fall inside the patient and require retrieval.
Product
HF Resection Electrodes - HF resection electrodes are part of a resectoscope system for endoscopic diagnosis and treatment in urological or gynecological applications. 64 Models: 1) A22201C 2) A22201D 3) A22202C 4) A22203C 5) A22205C 6) A22205D 7) A22206C 8) A2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1429-2023·2023-08-23
Romaine Lettuce Recalled Due to Potential Deer Feces Contamination
G.O. Corporation is recalling Romaine Lettuce All American sold in four states due to potential contamination with deer feces.
Product
Lettuce Romaine All American, packaged in the following sizes and configurations: 1. Produce Code 476702, 1-5 lb. bag per shipping case, Customer UPC 8398299; 2. Produce Code 476709, 4-5 lb. bags per shipping case, Customer UPC 476709, 8336156, and 8398281.
Category
Food
Distribution
4 states
CriticalCPSC·23263·2023-08-17
Zipadee Kids Convertible House Bed Frames Recalled for Entrapment and Strangulation Risk
Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds are being recalled due to spindle spacing that can trap a child's torso while preventing their head from passing through, creating a strangulation hazard. At least two children have become entrapped.
Product
Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23783·2023-08-17
Ubio Labs power banks recalled due to fire hazard
Costco is recalling approximately 350,000 Ubio Labs power banks (model PWB1071) that can overheat and ignite. The company has received three fire reports, including one on a commercial flight with four smoke inhalation reports and one minor burn injury.
Product
Ubio Labs power banks
Category
Consumer Product
Distribution
Distributed nationwide

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16651–16675 of 27769