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

8801–8825 of 113902

HighFDA (Devices)·Z-1948-2025·2025-06-18
Solana Bordetella Complete Assay Kit Recalled for False Positive Results
Ortho-Clinical Diagnostics is recalling the Solana Bordetella Complete Assay Kit (Model M308) because it may produce false positive results for Bordetella parapertussis at a rate of up to 16.7%.
Product
Brand Name: Solana¿ Bordetella Complete Assay Product Name: Solana Bordetella kit Model/Catalog Number: M308 Software Version: not applicable Product Description: One sales unit (kit) contains materials for 48 tests. One kit contains 48 tubes of 1.45 mL Process Buffer and
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1940-2025·2025-06-18
Femoral Nail RIGHT T2 GTN 8x300 mm labeled incorrectly
Stryker GmbH is recalling Femoral Nail RIGHT T2 GTN 8x300 mm devices because some lots were labeled as left or right but contained the opposite orientation.
Product
Femoral Nail, RIGHT T2 GTN 8x300 mm. Catalog Number: 1851-0830S.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0460-2025·2025-06-18
Celecoxib Capsules Recalled for Foreign Tablet Contamination
AvKARE is recalling Celecoxib 200 mg capsules because one tadalafil 5 mg tablet was found in a 500-count bottle. The contamination poses a risk of unintended drug exposure to patients.
Product
CELECOXIB — CELECOXIB (CELECOXIB)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1917-2025·2025-06-18
SCD Comfort Knee Length sleeves recalled for software logic errors
Cardinal Health is recalling SCD Comfort Knee Length Small sleeves (SKU 84021) due to incorrect software logic that may cause frequent E1 errors and delay patient treatment.
Product
SCD Comfort Knee Length Small, SKU 84021; Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow Controller
Category
Medical Device
Distribution
5 states
HighFDA (Food)·H-0044-2025·2025-06-18
Post Honey Bunches of Oats with Almonds Cereal Recall
Post Consumer Brands is recalling Post Honey Bunches of Oats with Almonds cereal (48 oz boxes) due to the presence of metal fragments. Consumers who have purchased affected products should not consume them.
Product
Post Honey Bunches of Oats with Almonds. Sweetened Cereal with Oats and Honey. Net Wt 48 oz (3 lbs) 1.36kg. 2 Bags inside for freshness. UPC 8 84912-01428 3. Post Consumer Brands, LLC, Lakeville, MN 55044.
Category
Food
Distribution
2 states
ModerateFDA (Drugs)·D-0461-2025·2025-06-18
Chlorthalidone Tablets Recalled Due to Failed Dissolution Specifications
AvKARE is recalling Chlorthalidone Tablets USP 25 mg due to failed dissolution specifications. The defect may affect the drug's therapeutic effectiveness.
Product
CHLORTHALIDONE — CHLORTHALIDONE (CHLORTHALIDONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1947-2025·2025-06-18
Thermo SCIENTIFIC Sensititre Mueller-Hinton Broth diagnostic device recalled
Remel, Inc. is recalling one lot of Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth due to off-color that may affect performance of this in-vitro diagnostic device.
Product
Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; invitro diagnostic device
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0015-2025·2025-06-18
Comvita Manuka Honey Cordyceps recalled for faulty packaging seal
Comvita Manuka Honey + Cordyceps is being recalled due to a leaking induction seal on the packaging. The defect affects approximately 2,730 units distributed across multiple states.
Product
Comvita branded Manuka Honey + Cordyceps for energy; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode# 658196001037
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-0497-2025·2025-06-18
Icosapent Ethyl Capsules Recalled for Failed Tablet Specifications
Zydus Pharmaceuticals is recalling Icosapent Ethyl Capsules due to burnt or melted capsules caused by oxidation from leakage of capsule contents. The recall affects 11,616 bottles distributed in Illinois, Pennsylvania, and Mississippi.
Product
ICOSAPENT ETHYL — ICOSAPENT ETHYL (ICOSAPENT ETHYL)
Category
Drug
Distribution
3 states
ModerateFDA (Drugs)·D-0469-2025·2025-06-18
Cephalexin Oral Suspension Recalled for Failed Impurities Specifications
Ascend Laboratories is recalling Cephalexin for Oral Suspension due to an out-of-specification result in impurity testing that identified Cephalexin Glucose Adduct during stability analysis.
Product
CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0014-2025·2025-06-18
Comvita Manuka Honey Lion's Mane product recall packaging defect
Comvita Manuka Honey + Lion's Mane for Focus is recalled due to a leaking induction seal on the packaging. Approximately 2,730 units distributed across multiple U.S. states are affected.
Product
Comvita branded Manuka Honey + Lion's Mane for Focus; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode# 658196001020
Category
Food
Distribution
7 states
ModerateFDA (Food)·F-0932-2025·2025-06-18
Instant Milk Tea Taro Flavor Recalled for Undeclared Milk Allergen
R&M Refresher brand Instant Milk Tea Powder in Taro Flavor is recalled nationwide because the label does not declare milk, though the product contains Whey Powder and Sodium Caseinate derived from milk.
Product
Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLBH, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D72CMLBH 3-pack ASIN #B0D72D6589 Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder,
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0016-2025·2025-06-18
Comvita Manuka Honey + Reishi recalled for leaking induction seal
Comvita Manuka Honey + Reishi is recalled due to a leaking induction seal on the packaging. The product may not be properly sealed.
Product
Comvita branded Manuka Honey + Reishi; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode# 658196001013
Category
Food
Distribution
7 states
ModerateFDA (Devices)·Z-1967-2025·2025-06-18
Guardian System 2 Controller Software Battery Alert Display Issue
Turncare is recalling Guardian System 2 Controllers due to a software issue where low and terminal battery alerts do not display on the screen in certain circumstances when the device is not running patient therapy.
Product
Brand Name: Guardian 2 System Product Name: Guardian System 2 Controller Model/Catalog Number: GS-2.5-C Software Version: 2.5.4-59 (Fix)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1937-2025·2025-06-18
BD BBL CultureSwab EZ Collection and Transport System Swabs Breakage
BD BBL CultureSwab EZ Collection and Transport System (REF 220144) is being recalled because swabs may break during use. The recall affects units distributed nationwide in Maryland.
Product
BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1964-2025·2025-06-18
Baxter Novum IQ Syringe Pump Design Issue Recall
Baxter is recalling certain Novum IQ Syringe Pumps manufactured or repaired after July 4, 2023, due to a design issue that may falsely detect a syringe flange when none is loaded, causing the pump interface to become stuck or display a System Error 21502.
Product
Baxter Novum IQ Syringe Pump, product code 40800BAXUS,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0468-2025·2025-06-18
Cephalexin Oral Suspension Recalled for Failed Impurity Specifications
Ascend Laboratories is recalling Cephalexin for Oral Suspension due to failed impurity specifications identified during stability testing. An out-of-specification result for Cephalexin Glucose Adduct was observed at six months.
Product
CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1968-2025·2025-06-18
Guardian System 2 Controller units recalled for battery alert display defect
Turncare has recalled certain Guardian 2 System controllers because a software issue prevented "low" and "terminal" battery alerts from displaying on the screen in specific circumstances when the device was not running patient therapy.
Product
Brand Name: Guardian 2 System Product Name: Guardian System 2 Controller Model/Catalog Number: GS-2.5-C Software Version: 2.5.4-69 (Fix)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1926-2025·2025-06-18
DxI 9000 Access Immunoassay Analyzer software version 1.20 recall
Beckman Coulter is recalling certain DxI 9000 Access Immunoassay Analyzers due to incorrect motor/encoder and cable installation that causes error codes, prevents assays from running, and delays result generation.
Product
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software versions 1.20
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0041-2025·2025-06-18
Supreme Produce Celery & PB Snack Cup Recalled for Plastic
GBC Food Services is recalling Supreme Produce Celery & PB Snack Cup (9oz) due to the possible presence of plastic foreign material. Affected products have Best By dates from 4/12/2025 to 5/6/2025.
Product
Supreme Produce Celery & PB Snack Cup. Net Wt: 9oz (225g). Keep Refrigerated. UPC 8 50065-40308 3. GBC Food Services, 14043 Distribution Way, Farmers Branch, Texas
Category
Food
Distribution
4 states
ModerateFDA (Food)·H-0042-2025·2025-06-18
Supreme Produce Apple & PB Snack Cup Recalled for Plastic
GBC Food Services is recalling Supreme Produce Apple & PB Snack Cup due to possible plastic foreign material in the product. Affected units were distributed in GA, MI, IN, and TN with Best By dates from 4/12/2025 to 5/6/2025.
Product
Supreme Produce Apple & PB Snack Cup. Net Wt: 8oz (226g). Keep Refrigerated. UPC 8 50065-403 1. GBC Food Services, 14043 Distribution Way, Farmers Branch, Texas
Category
Food
Distribution
4 states
ModerateFDA (Food)·F-0930-2025·2025-06-18
Preconception Multi for Women 60 capsules Batch 42469 recalled
NRC Nutrition Pty Ltd is recalling Preconception Multi for Women 60 capsules, Batch 42469, due to inconsistent blending of iodine in the product.
Product
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Category
Drug
Distribution
5 states
ModerateFDA (Food)·F-0933-2025·2025-06-18
Instant Milk Tea Matcha Flavor recalled for undeclared milk allergen
R&M Refresher Instant Milk Tea Matcha Flavor is recalled because its label declares "Non-Dairy Creamer" but does not specify that the product contains milk (whey powder and sodium caseinate). The product may cause allergic reactions in consumers with milk allergies.
Product
Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y85TG, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D71Y85TG 3-pack ASIN #B0D71YBV1X Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder,
Category
Food
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0470-2025·2025-06-18
Levothyroxine Sodium tablets recalled for foreign substance contamination
Macleods Pharmaceuticals is recalling Levothyroxine Sodium 112 mcg tablets (Lot #MLF2401A, expiration 01/31/2026) distributed nationwide due to black hair found embedded in tablets.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0462-2025·2025-06-18
Ezetimibe and Simvastatin Tablets Recalled for Failed Impurity Specifications
Glenmark Pharmaceuticals Inc., USA is recalling Ezetimibe and Simvastatin Tablets (10mg/40mg) due to out-of-specification results for related substances in a stability study. The recall affects approximately 6,759 bottles distributed nationwide.
Product
EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
Category
Drug
Distribution
Distributed nationwide

How to read this listing

Filters

8801–8825 of 113902