The Recall Desk

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.

Filters

Agency

All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

126–150 of 5601

  • SevereFDA (Drugs)·D-0618-2026·2026-07-01

    Pediatric Total Parenteral Nutrition Bag Recalled for Incorrect Formulation

    Central Admixture Pharmacy Services recalls a patient-specific pediatric TPN (Total Parenteral Nutrition) bag because it did not contain copper and famotidine as labeled.

    Product
    Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Rx# 24-1269856-0-1Compound Volume 1295 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Boston, 55 6th Rd Woburn, Massachusetts 01801-1767
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2591-2026·2026-07-01

    Medline angiography and radiology convenience kits recalled for unapproved design changes

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and to Barbados.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO PACK DYNJ30565C DYNJ32555B ANGIO PACK-LF DYNJ0774765U ANGIO TRAY DYNJ46153A ANGIOGRAM TRAY DYNJ33638K ANGIOGRAPHY DRAPE PK QVH-LF DYNJ35110D ANGIOGRAPHY P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1122-2026·2026-07-01

    Sunflower Seeds Recalled for Undeclared Cashew Allergen

    George J Howe Company is recalling 5# Sunflower Seeds C/NS due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across 24 states.

    Product
    5# Sunflower Seeds C/NS
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·H-1081-2026·2026-07-01

    Joy Mango Lassi recalled due to inadequate pasteurization

    Joy Gourmet Foods LLC is recalling Joy Mango Lassi 16 oz. and 64 oz. beverages due to inadequate pasteurization, which may allow harmful bacteria to survive.

    Product
    Joy Mango Lassi 16 oz., 64 oz.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·H-1088-2026·2026-07-01

    Joy Mango-Pina-Orange Lassi Recalled for Inadequate Pasteurization

    Joy Gourmet Foods LLC is recalling Joy Mango-Pina-Orange Lassi in 16 oz. and 64 oz. sizes because the product was not adequately pasteurized. The affected bottles have expiry dates between June 30 and July 30, 2026.

    Product
    Joy Mango-Pina-Orange Lassi 16 oz., 64 oz.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·H-1103-2026·2026-07-01

    Spring & Mulberry Date-Sweetened Chocolate Recalled for Salmonella

    Spring & Mulberry Inc. is recalling Pure Dark and Pure Dark Minis date-sweetened chocolate products nationwide due to potential Salmonella contamination. Consumers should not consume the affected products and should discard or return them.

    Product
    1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a navy blue box, UPC 850055470002, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1113-2026·2026-07-01

    Zapp's Brand Bayou Blackened Ranch Potato Chips Recalled for Salmonella

    Utz Quality Foods is recalling Zapp's Brand Bayou Blackened Ranch Potato Chips in 2.5oz and 8oz bags due to potential Salmonella contamination. Affected products were distributed across 32 states.

    Product
    2.5oz , 8oz , Zapp's Brand Bayou Blackened Ranch Potato Chips, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2455-2026·2026-07-01

    Medline Convenience Kits Medical Devices Recalled for Quality Issues

    Medline Industries is recalling four models of Convenience Kits containing Lidocaine and Bupivacaine injections due to quality issues identified during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, Model Number: ACC010890; 2) OPEN HEART A OVERHEAD, Model Number: DYNJ910066; 3) OPEN HEART, Model Number: DYNJ9855016V; 4) OPEN HEART, Model Number: DYNJ9855016X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2574-2026·2026-07-01

    Dexcom G7 Continuous Glucose Monitoring System sensors recalled

    Dexcom is recalling two lots of G7 glucose sensors that were stolen during destruction and sold through unauthorized channels. These sensors were designated for destruction due to improper sterilization, increased infection risk, and potential for inaccurate or missing readings.

    Product
    Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US Retail Sensor/Transmitter 1-pack Model/Catalog Number: STP-AT-012 Software Version: N/A Product Description: Dexcom G7 US Retail Sensor/Transmitter 1-pack Component: Dexcom G7 Continuous Gl
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·H-1097-2026·2026-07-01

    Spring & Mulberry Mixed Berry Date-Sweetened Chocolate recalled for potential Salmonella

    Spring & Mulberry Inc. is recalling Spring & Mulberry Mixed Berry Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects approximately 66,779 individual bars distributed nationwide.

    Product
    Spring & Mulberry Mixed Berry Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470026, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indiv
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2454-2026·2026-07-01

    Medline Convenience Kits with Central Line Insertion recalled for quality issues

    Medline Industries is recalling two models of Convenience Kits (ACC011142 and DYNJ8407) distributed nationwide. The kits contain injectable anesthetics that were recalled due to quality issues found during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC011142; 2) CENTRAL AND ARTERIAL LINE TOTE, Model Number: DYNJ8407
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1106-2026·2026-07-01

    Spring & Mulberry Blood Orange Date-Sweetened Chocolate recalled for Salmonella

    Spring & Mulberry Inc. is recalling Blood Orange Date-Sweetened Chocolate bars due to potential Salmonella contamination. Affected products were distributed nationwide.

    Product
    Spring & Mulberry Blood Orange Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470200, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold in
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0624-2026·2026-07-01

    ChloraPrep One-Step Topical Antiseptic Recalled for Non-Sterility

    CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) topical applicators due to non-sterility caused by the presence of Aspergillus penicillioides fungal contamination.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0625-2026·2026-07-01

    ChloraPrep One-Step Antiseptic Solution Recall Due to Sterility Concerns

    CareFusion is recalling 178,000 ChloraPrep One-Step antiseptic applicators (Lot #4073005) nationwide due to potential non-sterility from fungal contamination and seal breaches from paper lidding wrinkles.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1101-2026·2026-07-01

    Spring & Mulberry Mulberry Fennel Chocolate Bars Recalled for Salmonella

    Spring & Mulberry Inc. is recalling Mulberry Fennel Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recalled product was distributed nationwide.

    Product
    Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a burgundy box, UPC 850055470149, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1105-2026·2026-07-01

    Spring & Mulberry Coffee Date-Sweetened Chocolate bars recalled for Salmonella

    Spring & Mulberry Inc. is recalling Spring & Mulberry Coffee Date-Sweetened Chocolate bars due to potential Salmonella contamination. The affected product was distributed nationwide.

    Product
    Spring & Mulberry Coffee Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light brown box, UPC 850055470224, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1112-2026·2026-07-01

    Zapp's Bayou Blackened Ranch Kettle Chips Recalled for Salmonella

    Utz Quality Foods, LLC is recalling 1.5oz bags of Zapp's Bayou Blackened Ranch Kettle Chips due to the potential presence of Salmonella. The product was distributed across 32 states.

    Product
    1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereCPSC·26527·2026-06-04

    Crenlux Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    Crenlux pool drain covers violate federal safety standards and pose risks of entrapment and drowning. About 200 units sold on Amazon from June 2025 through March 2026 are affected.

    Product
    Crenlux Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26524·2026-06-04

    Wyze Solar Cam Pan Security Cameras recalled for fire and burn hazard

    Wyze Labs is recalling about 321,360 Solar Cam Pan security cameras because incorrect assembly instructions can cause the lithium-ion battery to overheat and catch fire. The firm has received 13 reports of overheating, six of fires, and six reports of minor burns.

    Product
    Wyze Solar Cam Pan Security Cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26531·2026-06-04

    Residential Elevator Interlock Switches Recalled for Fall and Crushing Hazard

    SUNS International is recalling about 7,000 SS6291 Solenoid Interlock Switches used in residential elevators because they can become stuck, allowing the exterior door to remain unlocked and creating a risk of death or serious injury.

    Product
    SUNS SS6291 Solenoid Interlock Switches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26529·2026-06-04

    Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    Broqixin pool drain covers violate federal safety standards and pose a risk of serious injury or death from entrapment and drowning. About 370 units sold on Amazon from January to April 2026 should be removed immediately.

    Product
    Broqixin Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26532·2026-06-04

    Vornado SRTH Small Room Tower Heaters Recalled for Fire Hazard

    Vornado is recalling about 255,000 SRTH small room tower heaters because the fan blade can detach, causing overheating and fire. Vornado has received 32 overheating reports, including eight fires and one smoke inhalation.

    Product
    SRTH Small Room Tower Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide