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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

976–1000 of 26077

HighFDA (Food)·H-0665-2026·2026-04-22
Booey's Dragon's Breath sauce recalled for missing allergen declarations
Booey's Dragon's Breath sauce is recalled because the label fails to declare anchovy (fish) and sesame allergens in the allergen warning section, despite listing these ingredients. This poses a risk to consumers with fish and sesame allergies.
Product
Booey's Dragon's Breath sauce, 15.2oz ringneck glass bottle. UPC on bottle: 7 01936 29222 3. There are 12 bottles per case. Manufactured Exclusively for BOOEYS GOURMET 3924 N. Cannon St. Spokane, WA 99205. Label declares: INGREDIENTS: Contains Soy and Wheat. *** Soy Sauce (Wat
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1814-2026·2026-04-22
Medical imaging device may deliver unintended radiation exposure during 3D acquisitions
Siemens ARTIS Pheno imaging systems may expose patients to unintended low-dose radiation during 3D image acquisition due to unregulated radiation dose combined with system rotation. The recall affects 73 units distributed in the U.S. and internationally.
Product
ARTIS Pheno VE30A and VE40A, Model 10849000
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1824-2026·2026-04-22
CENTURION Circumcision Kits recalled for missing sterilization process
Medline's CENTURION Circumcision Kits (Lot 25KLA002) were distributed non-sterile. Healthcare facilities and patients who received them should not use the affected kits.
Product
CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1819-2026·2026-04-22
Cytal Burn Matrix recalled for out-of-specification endotoxin contamination
Integra LifeSciences Corp. is recalling Cytal Burn Matrix 7x10 cm burn treatment devices due to endotoxin contamination exceeding acceptable specifications. Seven units were distributed nationwide.
Product
Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1817-2026·2026-04-22
Cytal Wound Matrix 2-Layer Recalled for Out-of-Specification Endotoxin
Integra LifeSciences is recalling 46 units of Cytal Wound Matrix 2-Layer (Product ID: WSM0710) due to an increased rate of out-of-specification endotoxin results. The product was distributed nationwide across 31 states.
Product
Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1818-2026·2026-04-22
Cytal Wound Matrix 10x15 cm Recalled for Out-of-Specification Endotoxin
Integra LifeSciences has recalled Cytal Wound Matrix 2-Layer due to increased endotoxin levels above specification. The recall affects 452 units across 12 lot numbers distributed nationwide.
Product
Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0483-2026·2026-04-22
Epinephrine injection recalled for lack of sterility assurance
International Medication Systems Ltd. is recalling epinephrine injection due to lack of assurance of sterility. The recall affects 81,520 units of lot EA038A5 distributed nationwide.
Product
EPINEPHRINE — EPINEPHRINE (EPINEPHRINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0681-2026·2026-04-22
Pure Palm Medjool Dates Recalled for Coconut Allergen Mislabeling
Pure Palm Medjool Dates (UPC 852160007005, LOT PP0576D1) are being recalled because the product contains coconut but the label does not disclose this allergen, posing a risk to consumers with coconut allergies.
Product
Label is predominantly green with white lettering in a clear plastic clamshell container. Pure Palm dates- Medjool Dates Net Wt. 16OZ UPC: 852160007005
Category
Food
Distribution
0 states
HighFDA (Drugs)·D-0485-2026·2026-04-22
Memantine Hydrochloride Capsules Recalled for Failed Dissolution Specifications
The Harvard Drug Group LLC recalls Memantine Hydrochloride Extended-Release Capsules (7 mg, Lot N02425) distributed nationwide due to failed dissolution specifications that may impair drug absorption and efficacy.
Product
MEMANTINE HYDROCHLORIDE — MEMANTINE HYDROCHLORIDE (MEMANTINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0449-2026·2026-04-22
Cinacalcet tablets recalled due to N-nitroso impurity above acceptable limits
Cipla USA recalls Cinacalcet 30 mg tablets nationwide due to manufacturing deviations that resulted in N-nitroso Cinacalcet above acceptable daily intake limits. No illnesses have been reported.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0479-2026·2026-04-22
Albuterol Sulfate Inhalation Solution Recalled Due to Illegible Label
Nephron SC, LLC is recalling 146,280 vials of Albuterol Sulfate Inhalation Solution due to illegible labels. Illegible labels on prescription medications could prevent proper dosing and use.
Product
Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*), 30x5 mL Sterile Unit-Dose Vials, Rx only, nephron 503B Outsourcing facility, 4600 12th Street Extension, West Columbia, SC 29172, NDC 69374-330-05.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0471-2026·2026-04-22
Compounded Semaglutide Injectable Recalled Due to Sterility Failure
Payless Compounders is recalling a compounded semaglutide injectable due to lack of sterility assurance. The recall affects 91 vials distributed in Oregon.
Product
Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL vials, Rx only, Northwest Compounders, Beaverton, OR
Category
Drug
Distribution
1 state
HighFDA (Devices)·Z-1812-2026·2026-04-22
Endoscopic Clipping Device Recall Due to Malfunction Risk
Wilson-Cook Medical is recalling the Instinct Plus Endoscopic Clipping Device due to increased complaints indicating potential device malfunction. Approximately 713,702 units were distributed nationwide and internationally.
Product
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1820-2026·2026-04-22
Burn Matrix Medical Device Recalled for Out-of-Specification Endotoxin
Integra LifeSciences is recalling Cytal Burn Matrix devices due to out-of-specification endotoxin levels. The 226 affected units were distributed nationwide across 31 U.S. states and DC.
Product
Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1809-2026·2026-04-22
Insulin pump security vulnerability allows unauthorized access to dosing controls
Beta Bionics iLet Ace Pump Kit software versions 1.3.7, 1.4.2, and 1.4.3 contain a security flaw that allows status bar icons to bypass access screens. Unauthorized users could make unauthorized insulin delivery changes, risking severe hypoglycemia.
Product
iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0452-2026·2026-04-22
FHF Farmhouse Fresh acne lotion recalled for benzene contamination
Owen Biosciences is recalling 7,975 tubes of FHF Farmhouse Fresh Midnight Clearing Night Lotion nationwide due to benzene contamination. No illnesses have been reported. Consumers should stop using the affected product.
Product
FHF Farmhouse Fresh, Midnight Clearing, NIGHT LOTION, 2.5% BENZOYL PEROXIDE ACNE TREATMENT, OTC a) 0.5 fl. oz./15ml; and b)1 fl. oz./30ml tubes; Made in the USA for FarmHouse Fresh, 8797 CR 858 McKinney, Texas
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0451-2026·2026-04-22
Cinacalcet prescription drug recalled for nitrosamine impurity and manufacturing deviations
Cipla USA is recalling Cinacalcet Hydrochloride tablets due to the presence of N-Nitroso Cinacalcet above acceptable daily intake limits and manufacturing process deviations. The recall affects 63,192 bottles distributed nationwide.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0454-2026·2026-04-22
Acne Spot Treatment Recalled Nationwide for Benzene Contamination
SLMD BP Acne Spot Treatment (10% Benzoyl Peroxide, 15 mL bottles) is recalled due to benzene contamination. The recall affects 2,269 bottles distributed nationwide.
Product
SLMD BP Acne Spot Treatment, 10% Benzoyl Peroxide, 0.5 fl. oz - 15 mL bottles, Sandra Lee MD, Distributed by Skin PS Brands, Culver City, CA90232.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0459-2026·2026-04-22
Discount Drug Mart Cough Drops Recalled for Manufacturing Quality Concerns
Discount Drug Mart Cough Drops (Honey Lemon) nationwide recall at FDA recommendation following manufacturing facility inspection observations.
Product
DISCOUNT DRUG MART — DISCOUNT DRUG MART (COUGH DROPS HONEY LEMON)
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·26409·2026-04-16
nvyue Magic Pocket Staffs Recalled Due to Projectile and Laceration Hazards
nvyue Magic Pocket Staffs are being recalled after 163 reported injuries from sudden expansion despite protective pins. Injuries include corneal lacerations, temporary vision loss, and cuts requiring stitches, affecting children as young as nine.
Product
nvyue Magic Pocket Staffs
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26414·2026-04-16
SEGMART 55-Inch Mini Toddler Trampolines Recalled for Strangulation Hazard
SEGMART is recalling about 1,200 mini trampolines sold at Walmart.com and TikTok Shop because children can become entangled in accessory straps (hammock, punching bag, hand rings), posing a strangulation hazard. One child suffered a rope burn around the neck from entanglement.
Product
SEGMART 55" Indoor/Outdoor Mini Round Toddler Trampolines with Enclosure Nets and Accessory Kits
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26413·2026-04-16
Children's Metal Multi-Point Swing Frames Recalled Due to Fall Hazard Risk
Fun and Function is recalling approximately 1,300 children's metal multi-point swing frames that can crack or break during use. The firm received 10 reports of frame cracks or breaks with children falling, resulting in 2 documented injuries.
Product
Multi-Point Swing Frames
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26423·2026-04-16
Sweetcrispy Electric Pressure Washers Recalled for Electrocution Hazards
Sweetcrispy is recalling electric pressure washers (model XCJ-K01) sold online because they lack ground-fault circuit-interrupter (GFCI) protection, creating a serious electrocution hazard. No injuries have been reported.
Product
Sweetcrispy Electric Pressure Washers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26419·2026-04-16
Fisher & Paykel Gas Ranges Recalled for Delayed Ignition Burn Hazard
About 433 Fisher & Paykel gas ranges are recalled due to delayed oven ignition causing gas accumulation and combustion, creating a burn hazard. One minor burn injury has been reported.
Product
Fisher & Paykel Gas Ranges
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26422·2026-04-16
Le Hao Tool Electric Pressure Washers Recalled for Electrocution Risk
Le Hao Tool electric pressure washers lack a ground-fault circuit-interrupter (GFCI), creating a serious risk of electrocution. About 3,100 units were sold online between November 2023 and January 2026.
Product
Le Hao Tool Electric Pressure Washers
Category
Consumer Product
Distribution
Distributed nationwide

Filters

976–1000 of 26077