1 recall — Utz Quality Foods, LLC
Potential presence of Salmonella.
Company / brand: Utz Quality Foods recalls
Official ID H-1112-2026 · Official record ↗
Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 2,001–2,100, newest first.
Potential presence of Salmonella.
Company / brand: Utz Quality Foods recalls
Official ID H-1112-2026 · Official record ↗
Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich
Company / brand: Produce Innovations recalls
Official ID H-1111-2026 · Official record ↗
Undeclared colors (FD&C Yellow 5 and FD&C Red 40).
Company / brand: Alb-USA Enterprises recalls
Official ID H-1110-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: Spring & Mulberry recalls
Official ID H-1106-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: Spring & Mulberry recalls
Official ID H-1105-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: Spring & Mulberry recalls
Official ID H-1104-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: Spring & Mulberry recalls
Official ID H-1103-2026 · Official record ↗
Potential Salmonella contamination.
Company / brand: Spring & Mulberry recalls
Official ID H-1102-2026 · Official record ↗
Potential Salmonella contamination.
Company / brand: Spring & Mulberry recalls
Official ID H-1101-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: Spring & Mulberry recalls
Official ID H-1100-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: Spring & Mulberry recalls
Official ID H-1099-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: Spring & Mulberry recalls
Official ID H-1098-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: Spring & Mulberry recalls
Official ID H-1097-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: Spring & Mulberry recalls
Official ID H-1096-2026 · Official record ↗
potential salmonella contamination
Company / brand: Champion Foods recalls
Official ID H-1095-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1094-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1093-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1092-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1091-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1090-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1089-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1088-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1087-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1086-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1085-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1084-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1083-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1082-2026 · Official record ↗
Product not adequately pasteurized
Company / brand: Joy Gourmet Foods recalls
Official ID H-1081-2026 · Official record ↗
Improperly eviscerated which may result in Clostridium botulinum contamination
Company / brand: Prime Food Processing recalls
Official ID H-1080-2026 · Official record ↗
Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0628-2026 · Official record ↗
sub potency
Company / brand: Elevate Oral Care recalls
Official ID D-0627-2026 · Official record ↗
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
Company / brand: Annora Pharma Private recalls
Official ID D-0626-2026 · Official record ↗
Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
Company / brand: CareFusion 213 recalls
Official ID D-0625-2026 · Official record ↗
Non-Sterility: Due to presence of Aspergillus penicillioides.
Company / brand: CareFusion 213 recalls
Official ID D-0624-2026 · Official record ↗
Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
Company / brand: CareFusion 213 recalls
Official ID D-0623-2026 · Official record ↗
Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
Company / brand: CareFusion 213 recalls
Official ID D-0622-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: PReye recalls
Official ID D-0621-2026 · Official record ↗
Presence of foreign substance
Company / brand: ANI Pharmaceuticals recalls
Official ID D-0619-2026 · Official record ↗
Incorrect product formulation: bag did not contain copper and famotidine per label.
Company / brand: Central Admixture Pharmacy Services recalls
Official ID D-0618-2026 · Official record ↗
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Company / brand: Direct Rx recalls
Official ID D-0617-2026 · Official record ↗
CGMP Deviations
Company / brand: Amgen recalls
Official ID D-0616-2026 · Official record ↗
Presence of Foreign Substance.
Company / brand: Amgen recalls
Official ID D-0615-2026 · Official record ↗
CGMP Deviations
Company / brand: Amgen recalls
Official ID D-0614-2026 · Official record ↗
CGMP Deviations
Company / brand: Amgen recalls
Official ID D-0613-2026 · Official record ↗
Presence of Foreign Substance.
Company / brand: Amgen recalls
Official ID D-0612-2026 · Official record ↗
CGMP Deviations
Company / brand: Ajanta Pharma USA recalls
Official ID D-0611-2026 · Official record ↗
Subpotent Drug
Company / brand: The Harvard Drug Group recalls
Official ID D-0609-2026 · Official record ↗
A vehicle that does not make a sound may fail to alert pedestrians of an approaching vehicle, increasing the risk of a crash or injury.
Company / brand: Teko recalls
Official ID 26V420000 · Official record ↗
A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.
Company / brand: Nissan North America recalls
Official ID 26V419000 · Official record ↗
Windshield wipers or a washing system that fails to function as intended can reduce visibility, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V418000 · Official record ↗
Differential pinion shaft fracture may result in a loss of drive power, or unintended vehicle movement if the vehicle is in park without the parking brake applied, increasing the r…
Company / brand: Ford Motor Company recalls
Official ID 26V417000 · Official record ↗
A dinette that moves during transit may increase the risk of injury.
Company / brand: Jayco recalls
Official ID 26V416000 · Official record ↗
A vehicle that does not produce a warning sound may fail to alert pedestrians of an approaching vehicle, increasing the risk of injury.
Company / brand: Ford Motor Company recalls
Official ID 26V415000 · Official record ↗
A loss of electronic stability control and/or electronic brake assist increases the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26V414000 · Official record ↗
A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26V413000 · Official record ↗
An instrument panel display that does not show critical information, such as gear selection, increases the risk of a crash.
Company / brand: Nissan North America recalls
Official ID 26E039000 · Official record ↗
An overheated printed circuit board increases the risk of a fire.
Company / brand: Tiffin Motorhomes recalls
Official ID 26V412000 · Official record ↗
Referencing incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.
Company / brand: Jayco recalls
Official ID 26V411000 · Official record ↗
An unexpected loss of drive power can increase the risk of a crash. In addition, a driveshaft that is not fully engaged can result in a vehicle rollaway if the parking brake is not…
Company / brand: Nissan North America recalls
Official ID 26V410000 · Official record ↗
While using the pole rack at full capacity, an incorrect high vertical center of gravity during braking and cornering may lead to a loss of vehicle control, increasing the risk of …
Company / brand: Altec Industries recalls
Official ID 26V409000 · Official record ↗
A door that fails to open or close increases the risk of injury to occupants in a crash.
Company / brand: Daimler Trucks North America recalls
Official ID 26V408000 · Official record ↗
A door that fails to open or close increases the risk of injury to occupants in a crash.
Company / brand: Daimler Trucks North America recalls
Official ID 26V407000 · Official record ↗
An unsecured wheelchair can move during transit, increasing the risk of injury.
Company / brand: Diamond Coach recalls
Official ID 26V406000 · Official record ↗
The recalled detectors can fail to alert consumers of a fire, posing a risk of serious injury or death from smoke inhalation or burns.
Company / brand: Treatlife Technology Co recalls
Official ID 26582 · Official notice ↗
The heating element can remain energized during a ground fault, despite being turned off, posing a risk of fire or burn injury to consumers.
Company / brand: Daikin Comfort Technologies Manufacturing recalls
Official ID 26581 · Official notice ↗
The LED party favors violate the mandatory safety standard for consumer products because the battery compartment within the light-up products contains button cell batteries that ca…
Company / brand: ABGA Advanced Trading Co recalls
Official ID 26580 · Official notice ↗
The busy boards violate the mandatory safety standard for toys because magnets can detach, posing a deadly ingestion hazard. When high-powered magnets are swallowed, the ingested m…
Company / brand: Lesonic Technology Co recalls
Official ID 26579 · Official notice ↗
The recalled sneakers violate the mandatory standard for consumer products with button cell and coin batteries because the lithium coin batteries can be accessed easily by children…
Company / brand: Shenzhen Qicheng Trading Co recalls
Official ID 26578 · Official notice ↗
The baby oil contains low-viscosity hydrocarbons, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The baby oil's packaging is not ch…
Company / brand: Shield Line recalls
Official ID 26577 · Official notice ↗
The roll-on warmers' power cord can overheat and short circuit, posing a risk of serious injury or death from fire, burn and electrical shock hazards.
Company / brand: Southern Telecom recalls
Official ID 26576 · Official notice ↗
The solar power bank's lithium-ion battery can swell and overheat, posing a burn hazard to consumers.
Company / brand: Spector & Co recalls
Official ID 26575 · Official notice ↗
The recalled youth ATVs violate the mandatory safety standard for ATVs because they are missing brake lights, reducing visibility of the youth ATV to other vehicles, posing a deadl…
Company / brand: Yongkang Ruihe Metal Products Co recalls
Official ID 26574 · Official notice ↗
The recalled children's loungewear sets violate the mandatory flammability standards for children's sleepwear, posing a risk of serious burn injuries.
Company / brand: Kith Retail of Brooklyn recalls
Official ID 26507 · Official notice ↗
Broken or loose steering gear bolts can cause a loss of steering control, increasing the risk of a crash.
Company / brand: Harbinger Motors recalls
Official ID 26V405000 · Official record ↗
The defective batteries may overheat, increasing the risk of a fire.
Company / brand: Elgin Sweeper Company recalls
Official ID 26V404000 · Official record ↗
A detached fender flare can become a road hazard and increase the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V403000 · Official record ↗
Park system damage may result in a vehicle rollaway, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V402000 · Official record ↗
An overheated printed circuit board increases the risk of a fire.
Company / brand: Airstream recalls
Official ID 26V401000 · Official record ↗
An instrument panel display that fails to show critical safety information, such as the speedometer or warning lights, increases the risk of a crash.
Company / brand: Hyundai Motor America recalls
Official ID 26V400000 · Official record ↗
Due to 11 volt Backup Battery failures.
Company / brand: Thoratec recalls
Official ID Z-2520-2026 · Official record ↗
Due to 11 volt Backup Battery failures.
Company / brand: Thoratec recalls
Official ID Z-2519-2026 · Official record ↗
Due to 11 volt Backup Battery failures.
Company / brand: Thoratec recalls
Official ID Z-2518-2026 · Official record ↗
Due to unsealed portions of pouches.
Company / brand: Merit Medical Systems recalls
Official ID Z-2517-2026 · Official record ↗
Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By D…
Company / brand: Inspire Medical Systems recalls
Official ID Z-2516-2026 · Official record ↗
Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By D…
Company / brand: Inspire Medical Systems recalls
Official ID Z-2515-2026 · Official record ↗
Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has …
Company / brand: BD SWITZERLAND SARL recalls
Official ID Z-2514-2026 · Official record ↗
The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfu…
Company / brand: Beta Bionics recalls
Official ID Z-2513-2026 · Official record ↗
Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses.
Company / brand: Staar Surgical AG recalls
Official ID Z-2509-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2508-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2507-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2506-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2505-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2504-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2503-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2502-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2501-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2500-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2499-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2498-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.