The Recall Desk
US Product Recalls, Verified and Explained
Plain-English summaries of US product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — always linked back to the original government notice. Severity is scored from objective criteria, never vibes.
- Recalls tracked
- 113,671
- Agencies monitored
- 5
- Most recent announcement
- Sep 9, 2026
Critical now
See all critical →Severity-5 recalls announced in the last 30 days. These involve documented or strongly suspected risk of serious injury or death.
- CriticalFDA (Food)·2026-09-02Sirna & Sons Jalapeno Peppers Recalled for Potential Salmonella Javiana
- CriticalFDA (Food)·2026-09-02FDA Recalls Addall XR Shot Liquid Dietary Supplement
- CriticalFDA (Food)·2026-09-02FDA Recalls Glutinous Rice Balls with Undeclared Peanuts
- CriticalFDA (Food)·2026-09-02Jaime's Foods ATX Recalls Jalapeno Ranch Due to Undeclared Egg Allergen
- CriticalFDA (Food)·2026-08-26Whole Foods Guacamole Recalled for Potential Salmonella Contamination
Most severe recent recalls
See all →- CriticalFDA (Food)
Jaime's Foods ATX Recalls Jalapeno Ranch Due to Undeclared Egg Allergen
Jaime's Foods ATX, LLC is recalling Jalapeno Ranch in 16 oz. glass jars because the product contains an undeclared egg allergen. The recall affects 102 cases distributed in Texas.
2026-09-02
- CriticalFDA (Food)
Sirna & Sons Jalapeno Peppers Recalled for Potential Salmonella Javiana
Sirna & Sons Produce is recalling 249 bags of 1 lb jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed for food service use in Ohio and Pennsylvania.
2026-09-02
- CriticalFDA (Food)
FDA Recalls Addall XR Shot Liquid Dietary Supplement
ZMB Enterprises is recalling Addall XR Shot liquid dietary supplements because they contain undeclared ingredients 1,4-DMAA, Phenylethylamine, and Phenibut.
2026-09-02
By category
- Food recalls30447 records
FDA + USDA FSIS recalls of human food products.
- Drug recalls17978 records
FDA recalls of prescription and over-the-counter drugs.
- Medical device recalls39923 records
FDA recalls of medical devices including diagnostics, implants, and consumer health hardware.
- Vehicle recalls15364 records
NHTSA recalls of passenger vehicles, motorcycles, tires, and child seats.
- Consumer product recalls9950 records
CPSC recalls of household, juvenile, recreational, and electrical consumer products.
By agency
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Set up recall alerts →Why plain-English recalls matter
Government recall notices are written for compliance, not for shoppers. A typical FDA enforcement report identifies a product by its 21 CFR regulatory citation, the firm’s establishment number, the drug’s NDC code, and a one-line hazard description in regulatory shorthand. NHTSA notices use the NHTSA Campaign Number and reference Federal Motor Vehicle Safety Standards by number. None of that helps you decide whether the bag of spinach in your fridge or the car parked in your driveway is the one being recalled.
We translate every notice into a one-paragraph summary that tells you what the product is, what the hazard is, who’s at risk, and what to do. The full agency notice is one click away on every recall page, and the raw source data — UPC codes, lot numbers, distribution states, establishment numbers — is preserved verbatim so you can verify a recall against the product in front of you.
How we score severity
Every recall is scored 1 to 5 against objective criteria — agency classification, documented injuries or deaths, distribution scope, and hazard type. If the agency classified the recall Class I or if deaths are reported in the source text, the score is at least 4 regardless of other factors. If the source text explicitly says no illnesses have been reported and the hazard is theoretical, the score is capped at 3. Our reasoning is shown on every recall page in the “why this score” block. The methodology page has the full rubric.