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

7851–7875 of 89529

CriticalFDA (Devices)·Z-1289-2025·2025-03-19
Portex Endotracheal Tubes may deliver inadequate ventilation due to smaller diameter
Portex Endotracheal Tubes from Smiths Medical ASD, Inc. may have a smaller diameter than expected, potentially causing inadequate ventilation and patient hypoxia.
Product
Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127/035 100/141/025 100/141/030 100/141/035
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0633-2025·2025-03-19
Ulker Biskrem Cocoa Biscuits Recalled for Undeclared Wheat and Egg
ZB Importing LLC recalls Ulker Biskrem Cocoa Biscuits due to undeclared wheat and egg. Consumers with these allergies should not consume the product.
Product
Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628
Category
Food
Distribution
36 states
CriticalFDA (Food)·F-0609-2025·2025-03-19
Aleppo Tahini Sesame Paste recalled due to Salmonella contamination
Turkana Food Inc. is recalling Aleppo Tahini Sesame Paste because the product tested positive for Salmonella. The recalled product was distributed to 23 states.
Product
Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case
Category
Food
Distribution
23 states
SevereFDA (Food)·F-0631-2025·2025-03-19
Ulker Rulokat hazelnut wafers recalled nationwide for undeclared egg allergen
Ulker Rulokat Hazelnut Wafers are being recalled due to undeclared egg. The product was distributed to retail stores across Canada and 35 US states.
Product
Ulker Rulokat Hazelnut Wafers, item 3865, 6oz plastic cylinder, 6 per case, UPC 8690766086473
Category
Food
Distribution
36 states
SevereFDA (Food)·F-0637-2025·2025-03-19
Little Leaf Farms Southwest Salad Kit Recalled for Undeclared Fish and Wheat
Little Leaf Farms Southwest Salad Kit may contain incorrect dressing with undeclared fish and wheat. The recalled lot was distributed in Massachusetts, New Hampshire, and Connecticut.
Product
Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220
Category
Food
Distribution
3 states
SevereNHTSA·25V173000·2025-03-19
Nissan and INFINITI front brake calipers may break losing braking
Nissan is recalling certain 2025 Murano, Pathfinder and INFINITI QX60 vehicles because one or both front brake caliper assemblies may have reduced strength and could break, failing FMVSS 135.
Product
INFINITI — INFINITI, NISSAN QX60, PATHFINDER, MURANO
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1306-2025·2025-03-19
Aortic Root Cannula Recall for Loose Male Luer Component
Medtronic is recalling 316,205 aortic root cannulas due to unexpected loose material in the male luer connector. If not identified before use, this defect could cause stroke; if identified, it may delay surgery.
Product
Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014 AR FLOWGUARD 14GA, model no. 11014 2. MiAR Cannula: A. CANNULA 11012L AR FLOWGUARD LONG 12GA, model no 11012L B. CANNULA 11014L AR FLOWGUARD 14FR LONG, m
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0272-2025·2025-03-19
Injectable Phenylephrine Solution Recalled Due to Particulate Matter Contamination
The FDA is recalling phenylephrine injection solution due to particulate matter contamination. Three lot numbers distributed nationwide are affected.
Product
PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, 855-275-2270, NDC 71285-6092-1.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0268-2025·2025-03-19
Potassium Chloride Injection Strength Mislabeled on Packaging Overwrap
ICU Medical recalls Potassium Chloride Injection (lot 1023172) whose overwrap labeled as 10 mEq may contain 20 mEq containers, creating overdose risk. Product distributed nationwide.
Product
POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0636-2025·2025-03-19
Mauna Loa Milk Chocolate Macadamias recalled for undeclared almonds
Mauna Loa Macadamia Nut Company is recalling Milk Chocolate Covered Macadamias due to undeclared almonds. The product may cause allergic reactions in consumers with almond or tree nut allergies.
Product
Mauna Loa Milk Chocolate Covered Macadamias product is a snack product and packaged in plastic 1oz pouch. Each carton contains 12 pouches, and each master case contains 12 cartons. Retail Pouch (1oz pouch) UPC: 0 72992 04260 3 Carton (12 pouches) UPC: 72992 04261 Master Case (12
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-1304-2025·2025-03-19
BD Alaris Systems Manager Infusion Software Affected by Programming Request Issue
BD Alaris Systems Manager software may transmit outdated automated programming requests to progressive care units. The FDA has classified this as a Class I recall.
Product
BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
Category
Medical Device
Distribution
21 states
SevereFDA (Drugs)·D-0259-2025·2025-03-19
ChloraPrep One-Step Topical Drug Recalled for Fungal Contamination
CareFusion 213, LLC is recalling ChloraPrep One-Step, a preoperative skin preparation drug, due to non-sterility from a package lidding breach allowing fungal contamination. The recall affects 205,440 applicators distributed nationwide and in Canada.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0267-2025·2025-03-19
Potassium Chloride Injection Recalled: Overwrap Labeling Shows Incorrect Strength
ICU Medical recalls Potassium Chloride 20 mEq IV injection due to mislabeled overwrap showing 10 mEq instead of the correct strength. The correct dose is printed on the actual container.
Product
POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25E020000·2025-03-19
ZF Recalls Lemförder and TRW Track Control Arms for Subframe Cracking Risk
ZF North America is recalling specific Lemförder and TRW track control arms because a short bushing sleeve may crack the subframe, potentially causing loss of vehicle control.
Product
SUSPENSION:FRONT:CONTROL ARM recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0608-2025·2025-03-19
Raisin Bran Muffins Recalled Due to Undeclared Walnut Allergen
JE Bakery 2019 LLC is recalling Raisin Bran muffins sold under Cub Foods, Jerrys Foods, and County Market brands due to undeclared walnuts. The product was distributed in Minnesota and Wisconsin.
Product
Raisin Bran muffins, 6 count. Net Wt. 12.0 oz (0.75 lb) UPC 0 29341-00233 7. Labeled with the following store brands: Cub Foods, Jerrys Foods, and County Market
Category
Food
Distribution
2 states
SevereNHTSA·25V128000·2025-03-19
Vermeer Recalls 2020-2025 Vacuum Excavator Trailers Due to Frame Cracking
Vermeer is recalling 2020-2025 LPSDT, LPSGT, and LPXDT vacuum excavator trailers because the frame may crack or break, reducing stability while being towed.
Product
VERMEER — VERMEER LPSGT, LPXDT, LPSDT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1305-2025·2025-03-19
BD Care Coordination Engine Software May Send Outdated Programming Requests
BD Care Coordination Engine infusion software may send outdated automated programming requests to care units. Healthcare facilities in affected US states should review their systems.
Product
BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management Software
Category
Medical Device
Distribution
21 states
HighFDA (Devices)·Z-1327-2025·2025-03-19
Blood Pump Recalled for Potential Fluid Leakage During Clinical Use
Spectrum Medical is recalling Quantum Perfusion blood pumps due to potential fluid leakage during priming or clinical use. The issue affects approximately 1,487 units distributed nationwide.
Product
Brand Name: Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors Product Name: Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type Model/Catalog Number: CP22V-VT Software Version: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1315-2025·2025-03-19
Cartilage Transplant System Disposable Kits Recalled for Missing Component
DePuy Mitek is recalling COR Disposable Kit cartilage transplant systems because some units lack the pin in the graft loader component. The manufacturing defect may prevent proper device function during surgical use.
Product
COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0624-2025·2025-03-19
Green Chile Bean Burritos Recalled for Undeclared Milk Allergen
Mi Ranchito Foods is recalling Green Chile Bean Burritos because milk is not listed in the ingredient statement, posing a risk for consumers with milk allergies.
Product
Green Chile Bean Burrito, 15 days refrigerated at 33 45 degrees Fahrenheit. 120 days frozen at or below 32 degrees Fahrenheit. Packaged in cellophane wrapper. Net wt. 10 ounces, UPC #21856 11136. Mi Ranchito Foods, Inc. 606 Central Avenue, Bayard, NM 88023
Category
Food
Distribution
1 state
HighFDA (Drugs)·D-0261-2025·2025-03-19
Drug Recall: Alprostadil Affected by Manufacturing Practice Deviations
Alprostadil 3.0 gm is being recalled due to manufacturing practice deviations. Limited distribution affects product with lot number HAALC0020922 (expiration August 2025).
Product
Alprostadil Container Description: Amber color bottle
Category
Drug
Distribution
1 state
HighFDA (Devices)·Z-1324-2025·2025-03-19
Philips Spectral CT on Rails software recall due to scanning and movement issues
Philips is recalling one unit of Spectral CT on Rails software version 5.1.0 due to multiple software problems causing scanning issues, image errors, and unintended device movement.
Product
Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334;
Category
Medical Device
Distribution
1 state
HighFDA (Food)·F-0612-2025·2025-03-19
Trader Joe's Solid White Albacore Tuna Recalled for Defective Lid
Trader Joe's Solid White Albacore Tuna (5 oz cans) is being recalled due to improperly secured lids that may allow contamination with Clostridium botulinum. Affected products have Best By dates of 01/08/2028 or 01/09/2028.
Product
Trader Joe's branded Solid White Albacore Tuna in Water, no salt added; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 0099 2848
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0616-2025·2025-03-19
H-E-B Albacore Tuna recalled due to improper lid sealing and botulism risk
H-E-B branded Solid White Albacore Tuna is being recalled because its easy-pull lid may not be properly secured, risking contamination with Clostridium botulinum. The recalled products were distributed nationwide.
Product
HEB branded Solid White Albacore Tuna in water; Wild Caught; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Made with Pride and Care for H-E-B, San Antonio, TX 78204 UPC# 41220 14184 (can); UPC# 41220 43345 (4 pack shrink pack) Chunk White Albacore Tuna in water; wild caught; NET WT.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0618-2025·2025-03-19
Trader Joe's Solid White Albacore Tuna Recalled for Botulism Risk
Trader Joe's branded Solid White Albacore Tuna is being recalled because the easy-pull lids were not properly secured, potentially allowing Clostridium botulinum contamination. Approximately 14,147 cases were distributed nationwide.
Product
Trader Joe's branded Solid White Albacore Tuna in water, Low sodium; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 95836
Category
Food
Distribution
Distributed nationwide

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7851–7875 of 89529