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

3326–3350 of 6105

CriticalFDA (Food)·F-0925-2023·2023-05-31
Lay's Potato Chips Recalled for Undeclared Milk Allergen
Frito-Lay is recalling Lay's Classic Potato Chips due to undeclared milk. The recall affects specific products distributed in Connecticut, Massachusetts, Maine, and New Hampshire.
Product
Lay s Classic Party Size Potato Chips 13 oz. (368.5 g) UPC 028400310413 packaged in a yellow flexible bag and Lay s Classic Mix and Match Potato Chips 15 5/8 oz (442.9 g) UPC 0028400720151 packaged in a yellow flexible bag
Category
Food
Distribution
0 states
CriticalFDA (Devices)·Z-1618-2023·2023-05-31
Pediatric Ventricular Assist Device Blood Pumps Recalled for Potential Membrane Disruption
BERLIN HEART GMBH recalls EXCOR Pediatric Ventricular Assist Device Blood Pumps due to potential disruption in triple-layer membranes. The 335 affected units were distributed to multiple US states and Canada.
Product
EXCOR Pediatric Ventricular Assist Device Blood Pumps, Models: P10P-001 (10 ml blood pump); P15P-001 (10 ml blood pump); P25P-001x01 (25 ml blood pump); P30P-001x01 (30 ml blood pump), P50P-001 (50 ml blood pump); P60P-001 (60 ml blood pump). Recall occurred in 2018, and was r
Category
Medical Device
Distribution
16 states
SevereFDA (Food)·F-0924-2023·2023-05-31
Lancaster Spinach Recalled for Possible Listeria Contamination
Lancaster Spinach, 10-ounce packages, is recalled due to possible contamination with Listeria monocytogenes. Products were distributed in Massachusetts, Maryland, Pennsylvania, New York, New Jersey, and Virginia.
Product
LANCASTER SPINACH, 10 OZ, UPC:8-13055-01145-3. Packaged in sealed plastic bags, 12 in a case.
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-1594-2023·2023-05-31
COVID-19 At-Home Test Kits Recalled for Bacterial Buffer Contamination
SD Biosensor is recalling 2,712,767 Pilot COVID-19 At-Home Test kits nationwide due to bacterial contamination in the liquid buffer component. Users may notice an odor from affected kits.
Product
Pilot COVID-19 At-Home Test, Reference Number 9901-NCOV-10G, Catalog Number 99COV200L-EN02, UPC Code: 887473000207 (EAN-13: 08800111707728)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0929-2023·2023-05-31
Washington Crab Crabcakes Recalled Due to Undeclared Allergens
Washington Crab & Seafood Company recalls crabcakes due to undeclared allergens: egg, wheat, and soy. The product was distributed to North Carolina and South Carolina.
Product
CRABCAKE Ingredients: Blue Crabmeat, mayonnaise, onion bread crumbs, egg solids, salt, spices paprika WASHINGTON CRAB Carolina seafood
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0923-2023·2023-05-31
Collard Greens Recalled Due to Possible Listeria Contamination
Lancaster Foods is recalling Robinson Fresh and Giant collard greens due to possible contamination with Listeria monocytogenes. Affected products distributed in the Northeast and Mid-Atlantic should not be consumed.
Product
ROBINSON FRESH COLLARD GREENS, 16 OZ, UPC:0-95829-60006-7. Packaged in sealed plastic bags, 8 in a case. GIANT COLLARD GREENS, 16 OZ, UPC: 6-88267-05311-5. Packaged in sealed plastic bags, 8 in a case.
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0932-2023·2023-05-31
Ultra Tuna Salad Sandwich recall: undeclared egg and wheat allergens
Ultra Tuna Salad Sandwich sold in Washington contains undeclared egg and wheat allergens. The label fails to declare these common allergens, posing a risk to allergic consumers.
Product
Ultra Tuna Salad Sandwich, brand DishD'Lish. The label declares Albacore Tuna with Fresh Herbs, Mayo, Capers, Cucumbers, and pickles on Organic Whole Grain Bread. Served with Sweet Pickle Chips.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0921-2023·2023-05-31
Multiple kale greens products recalled for possible Listeria contamination
Lancaster Foods LLC is recalling ROBINSON FRESH and LANCASTER kale greens products due to possible Listeria monocytogenes contamination. Affected products have a best-by date of May 1, 2023, and were distributed in MA, MD, PA, NY, NJ, and VA.
Product
ROBINSON FRESH KALE GREENS, NET WT 16 OZ, UPC:0-95829-60015. Packaged in sealed plastic bags, 8 in a case. ROBINSON FRESH KALE GREENS NET WT 32 OZ UPC: 0-95829-60016-6. Packaged in sealed plastic bags, 8 in a case. LANCASTER Chopped Kale NET WT 4 OZ CHOPPED KALE. Packaged in
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0922-2023·2023-05-31
Giant Curly Leaf Spinach Recalled for Possible Listeria Contamination
Lancaster Foods LLC is recalling Giant Curly Leaf Spinach due to possible Listeria monocytogenes contamination. The product was distributed in MA, MD, PA, NY, NJ, and VA.
Product
GIANT CURLY LEAF SPINACH, 12 /8 OZ, UPC: 6-88267-09813-0. Packaged in sealed plastic bags, 12 in a case.
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0955-2023·2023-05-31
Safeway Oatmeal Raisin Cookies Recalled for Undeclared Peanut and Soy Allergens
Safeway brand Oatmeal Raisin Cookies (18 count) are being recalled due to undeclared peanut and soy allergens. Consumers with allergies to these ingredients should not consume the product.
Product
Oatmeal Raisin Cookies 18 Count, Safeway brand, packaged in a clear plastic hinged container, Net wt. 14oz. UPC 0 227862 70500 7. Distributed by Safeway Inc. Pleasanton, CA 94588. The Oatmeal Raisin scale label does include allergen advisory statement: Made in a facility that
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0928-2023·2023-05-31
Cole Slaw Recalled Due to Undeclared Egg and Soy Allergens
Washington Crab & Seafood Company recalls 463 cases of 16-ounce Cole Slaw sold in North Carolina and South Carolina. The product contains undeclared egg and soy allergens not listed on the label.
Product
COLE SLAW Ingredients: cabbage, mayonaise sugar, vinegar, celery seed, salt WT 16 oz WASHINGTON CRAB Carolina seafood
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0933-2023·2023-05-31
House Made Tarragon Chicken Salad Sandwich—undeclared egg and wheat allergens
FDA recalls House Made Tarragon Chicken Salad Sandwich by DishD'Lish because the label fails to declare egg and wheat, which are common allergens present in the product.
Product
House Made Tarragon Chicken Salad Sandwich, brand DishD'Lish. The label declares House Roasted Chicken Breast, Herbs, Fresh Tarragon, Arugula, Mayonnaise, and Whole Grain Bread.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0931-2023·2023-05-31
Tuna Salad Cup Recalled Due to Undeclared Egg Allergen
Ultra Tuna Salad Cup (DishD'Lish brand) distributed in Washington is recalled because the label does not declare egg as an ingredient. Consumers with egg allergies should not consume this product.
Product
Ultra Tuna Salad Cup, brand DishD'Lish, packaged in plastic cup. Label declares Housemade Albacore Tuna Salad, Arugula, Cucumber and Cherry Tomatoes.
Category
Food
Distribution
1 state
SevereNHTSA·23V384000·2023-05-30
2023 Toyota Corolla Cross instrument panel airbag deployment risk
Toyota is recalling 2022-2023 Corolla Cross vehicles because the instrument panel may lack required perforations, preventing proper front-passenger airbag deployment in a crash.
Product
TOYOTA — 2023 TOYOTA COROLLA CROSS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V373000·2023-05-25
2021-2023 Autocar Xpeditor trucks recalled for defective door latch
Autocar is recalling 2021-2023 Xpeditor commercial trucks due to incorrectly assembled right-side door latches that may open unexpectedly during operation. Owners should contact Autocar for a free inspection and reassembly.
Product
AUTOCAR — 2021 AUTOCAR XPEDITOR
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0893-2023·2023-05-24
SW Texas Nut Blend Recalled for Undeclared Almonds and Cashews
SW Texas Nut Blend (Item #5180819) is being recalled due to undeclared almonds and cashews. The product label lists only hazelnuts and walnuts as ingredients.
Product
SW Texas Nut Blend, Item #5180819, Packed in cardboard box with poly liner; net wt. 25 lbs. No UPC. Label declares: SW Texas Nut Blend, ingredients: Hazelnuts, Walnuts. Manufactured by: Ardent Mills Ave. Tualatin, OR.
Category
Food
Distribution
1 state
CriticalFDA (Food)·F-0885-2023·2023-05-24
Highkey Soft Baked Mini Treats recalled for undeclared egg allergen
Highkey Soft Baked Mini Treats Birthday Cake was recalled because egg allergen was not listed on the label, causing an allergic reaction in a consumer. The product was distributed to seven U.S. states.
Product
Highkey Soft Baked MINI TREATS BIRTHDAY CAKE NET WT 2 OZ (57g) CONTAINS: ALMONDS, MILD, AND COCONUT. DISTRIBUTED BY SUMMIT NATURALS INC ORLANDO, FL 32826 UPC 8 50020 43374 2
Category
Food
Distribution
7 states
CriticalFDA (Food)·F-0920-2023·2023-05-24
Gold Medal Flour Recalled Nationwide for Potential Salmonella Contamination
General Mills is recalling Gold Medal Bleached All Purpose Flour nationwide due to potential Salmonella contamination. Approximately 271,454 bags are affected.
Product
Gold Medal Bleached All Purpose Flour, Enriched, Presifted, packaged in the following sizes: 1. Net Wt 32 oz (2lb) 907g, UPC 0 16000-10710 6; and 2. Net Wt 5lb (2.26kg), UPC 0 16000-10610 9. Dist. By General Mills Sales, Inc., Minneapolis, MN 55440.
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1447-2023·2023-05-24
Draeger VentStar Anesthesia Breathing Circuit Connections May Detach
Draeger Medical recalls VentStar Anesthesia (N) 180 breathing circuits. Glued connections can loosen or detach during ventilation, potentially creating a critical disconnection risk.
Product
VentStar Anesthesia (N) 180, MP00333
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1440-2023·2023-05-24
Draeger VentStar Basic ventilator breathing circuit connections may detach during use
Draeger Medical is recalling 325 VentStar Basic (P)180 ventilators because glued breathing circuit connections can become loose before or during ventilation, potentially causing partial or complete detachment of circuit pieces.
Product
VentStar Basic (P)180, MP00351
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1460-2023·2023-05-24
Anesthesia circuit kit may detach during ventilation due to loose glued connections
Draeger Medical is recalling its Anesthesia Circuit Kit Coax HEPA (720 units) because glued connections can become loose during ventilation, potentially causing partial or complete detachment that could interrupt oxygen delivery during surgery.
Product
Anesthesia Circuit Kit Coax HEPA, MP17102
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1458-2023·2023-05-24
Anesthesia Set Coax 180 Breathing Circuit Connection Risk
Draeger Medical is recalling the Anesthesia Set Coax 180 because glued breathing circuit connections can become loose during ventilation, causing partial or complete detachment.
Product
Anesthesia Set Coax 180, MP03384
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1566-2023·2023-05-24
Plum A+ & A+3 Infusion System Batteries Recalled Due to Manufacturing Defect
ICU Medical Inc is recalling replacement batteries used in Plum A+ and A+3 infusion pump systems. A manufacturing defect may cause batteries to lose capacity earlier than expected.
Product
Replacement Battery List Number SUB0000594 found in Plum A+ & Plum A+3 Infusion Systems, List Numbers: a) 11005, b) 11971, c) 12391, d) 12618, e) 20678, f) 20679, g) 20792, h) 60629, i) 12348, j) 11973
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1567-2023·2023-05-24
ASM Replacement Battery Recalled for Manufacturing Defect and Capacity Loss
ICU Medical is recalling the ASM Replacement Battery due to a manufacturing defect from the battery supplier. The defect may cause batteries to lose capacity and experience decreased runtime earlier than expected.
Product
ASM Replacement Battery, Component Number SUB0000864
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1448-2023·2023-05-24
VentStar Basic Ventilator Recall: Risk of Breathing Circuit Detachment
Draeger Medical is recalling 1,725 VentStar Basic ventilators because glued breathing circuit connections can become loose and detach before or during ventilation. This may disrupt patient breathing support.
Product
VentStar Basic (N) 180, MP00353
Category
Medical Device
Distribution
Distributed nationwide

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3326–3350 of 6105