Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 1,001–1,100, newest first.
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Company / brand: Spectral Instruments recalls
Official ID Z-2939-2026 · Official record ↗
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may exp…
Company / brand: Bard Access Systems recalls
Official ID Z-2872-2026 · Official record ↗
Potential Salmonella contamination
Company / brand: GET FRESH PRODUCE recalls
Official ID H-1257-2026 · Official record ↗
Jalapenos may be contaminated with Salmonella.
Company / brand: Dairyland Produce recalls
Official ID H-1256-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1255-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1254-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1253-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1252-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1251-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1250-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1249-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1248-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1247-2026 · Official record ↗
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Company / brand: WFM Purchasing recalls
Official ID H-1246-2026 · Official record ↗
Potential foreign object contamination: rubber pieces
Company / brand: Gifford's Dairy recalls
Official ID H-1245-2026 · Official record ↗
Foreign object: May contain metal pieces
Company / brand: Grand Central Bakery - Oregon dba Grand Central Bakery recalls
Official ID H-1244-2026 · Official record ↗
Salmonella. The firm received a positive test result of Salmonella in the product.
Company / brand: Lidl US TRADING recalls
Official ID H-1243-2026 · Official record ↗
Potential Salmonella Javiana contamination
Company / brand: Coast Citrus Distributors recalls
Official ID H-1242-2026 · Official record ↗
Due to potential E. coli O145:H28 contamination
Company / brand: Publix Super Markets recalls
Official ID H-1241-2026 · Official record ↗
Due to potential E. coli O145:H28 contamination
Company / brand: Publix Super Markets recalls
Official ID H-1240-2026 · Official record ↗
Due to potential E. coli O145:H28 contamination
Company / brand: Publix Super Markets recalls
Official ID H-1239-2026 · Official record ↗
Due to potential E. coli O145:H28 contamination
Company / brand: Publix Super Markets recalls
Official ID H-1238-2026 · Official record ↗
Inaccurately declared nutrients including Iron (understated), and Vitamin D (overstated).
Company / brand: Prospector Popcorn recalls
Official ID H-1235-2026 · Official record ↗
Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated).
Company / brand: Prospector Popcorn recalls
Official ID H-1234-2026 · Official record ↗
Inaccurately declared nutrients including Potassium (overstated), Calcium (overstated), and Iron (understated).
Company / brand: Prospector Popcorn recalls
Official ID H-1233-2026 · Official record ↗
Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated).
Company / brand: Prospector Popcorn recalls
Official ID H-1232-2026 · Official record ↗
Soy not declared in the contains statement.
Company / brand: Nutrient Foods recalls
Official ID H-1231-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0802-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0801-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0800-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0799-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0798-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0797-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0796-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0795-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0794-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0793-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0792-2026 · Official record ↗
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Company / brand: American Regent recalls
Official ID D-0791-2026 · Official record ↗
Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.
Company / brand: Fresenius Kabi USA recalls
Official ID D-0788-2026 · Official record ↗
Failed Dissolution Specifications
Company / brand: Mylan Pharmaceuticals recalls
Official ID D-0774-2026 · Official record ↗
CGMP deviations: tablets with black specks.
Company / brand: Golden State Medical Supply recalls
Official ID D-0771-2026 · Official record ↗
CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0770-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Regeneron Pharmaceuticals recalls
Official ID D-0767-2026 · Official record ↗
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
Company / brand: Shilpa Medicare recalls
Official ID D-0765-2026 · Official record ↗
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
Company / brand: Shilpa Medicare recalls
Official ID D-0764-2026 · Official record ↗
Improperly tightened vehicle joints may lead to a loss of vehicle control, electrical failure, or detached parts, increasing the risk of a crash or fire.
Company / brand: Ford Motor Company recalls
Official ID 26V550000 · Official record ↗
A rearview image that does not display properly reduces the driver's view behind the vehicle, increasing the risk of a crash.
Company / brand: Mitsubishi Motors North America recalls
Official ID 26V549000 · Official record ↗
An unexpected loss of drive power increases the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V548000 · Official record ↗
A loss of driver power increases the risk of a crash. In addition, a loss of headlight function or windshield washing system function can reduce visibility, increasing the risk of …
Company / brand: Ford Motor Company recalls
Official ID 26V547000 · Official record ↗
A seat belt anchor with a missing connector plate may fail to properly restrain the driver and insufficient joint strength may not adequately protect passengers, increasing the ris…
Company / brand: Daimler Trucks North America recalls
Official ID 26V546000 · Official record ↗
A damaged subframe my lead to a loss of steering control, increasing the risk of a crash.
Company / brand: Rennline Automotive recalls
Official ID 26E060000 · Official record ↗
A child in the front seat may be at a greater risk of injury if the air bag deploys during a crash.
Company / brand: Kia America recalls
Official ID 26V545000 · Official record ↗
A short circuit increases the risk of a fire.
Company / brand: Paccar Incorporated recalls
Official ID 26V544000 · Official record ↗
Instability while towing increases the risk of a crash.
Company / brand: Cornell Pump Company recalls
Official ID 26V543000 · Official record ↗
An axle bracket that cracks or fails can result in a loss of control, increasing the risk of a crash.
Company / brand: T.a. Pelsue recalls
Official ID 26V542000 · Official record ↗
An improperly calibrated system may have a delayed braking response, increasing the risk of a crash.
Company / brand: Altec Industries recalls
Official ID 26V541000 · Official record ↗
A liftgate that falls unexpectedly increases the risk of injury.
Company / brand: Marathon Industries recalls
Official ID 26V568000 · Official record ↗
An overheated circuit increases the risk of a fire. A loss of the center brake light or front lights can also decrease visibility, increasing the risk of a crash.
Company / brand: Lucid Usa recalls
Official ID 26V540000 · Official record ↗
A rearview image that does not display correctly reduces the driver's view behind the vehicle, increasing the risk of a crash.
Company / brand: General Motors recalls
Official ID 26V539000 · Official record ↗
An overheated printed circuit board increases the risk of a fire.
Company / brand: Rossmonster Vans recalls
Official ID 26V538000 · Official record ↗
A child may fall after a partial detachment, increasing the risk of injury.
Company / brand: Britax Child Safety recalls
Official ID 26C006000 · Official record ↗
The recalled hockey visors and replacement visor accessories can crack upon impact, posing a risk of injury due to laceration or impact hazards.
Company / brand: CCM Hockey U.S recalls
Official ID 26716 · Official notice ↗
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or death from shock and ele…
Company / brand: Guangzhou Ao Lian Ya Wang Luo Ke Ji You Xian Gong Si recalls
Official ID 26715 · Official notice ↗
The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.
Company / brand: Dreams Bedding Technology PTE recalls
Official ID 26714 · Official notice ↗
The LED Tea Lights violate the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily by children, …
Company / brand: Shenzhen Jinhe Trade Co recalls
Official ID 26713 · Official notice ↗
The recalled power station's circuit board can overheat, posing a risk of serious injury from fire and burn hazards.
Company / brand: Goal Zero recalls
Official ID 26712 · Official notice ↗
The ventilation fan motor in the heat pumps can short circuit if water gets on the circuit board, causing the units to overheat and posing a fire hazard.
Company / brand: Modine Manufacturing Company recalls
Official ID 26711 · Official notice ↗
The rear brake caliper can crack or break, reducing the brake system's effectiveness, posing a risk of serious injury or death due to crash hazard.
Company / brand: KTM North America recalls
Official ID 26710 · Official notice ↗
The inability to extend or retract the outriggers can delay emergency response, increasing the risk of injury.
Company / brand: E-One Incorporated recalls
Official ID 26V537000 · Official record ↗
Unexpected vehicle movement may increase the risk of a crash.
Company / brand: Avride recalls
Official ID 26E059000 · Official record ↗
Undeclared Soy. Finished product ingredients statement declares Worcestershire sauce but does not declare sub-ingredients Soy Flavoring and Soy Lecithin.
Company / brand: Lyle Style recalls
Official ID EVT-99517-9nos1e · Official record ↗
Presence of Particulate Matter
Company / brand: Baxter Healthcare recalls
Official ID EVT-99463-1krekt6 · Official record ↗
Potential Cyclospora contamination.
Company / brand: Taylor Farms de Mexico S. de R.L. de C.V recalls
Official ID EVT-99453-wgl5uq · Official record ↗
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200 recalls
Official ID Z-2949-2026 · Official record ↗
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200 recalls
Official ID Z-2948-2026 · Official record ↗
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200 recalls
Official ID Z-2947-2026 · Official record ↗
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200 recalls
Official ID Z-2946-2026 · Official record ↗
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200 recalls
Official ID Z-2945-2026 · Official record ↗
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200 recalls
Official ID Z-2944-2026 · Official record ↗
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200 recalls
Official ID Z-2943-2026 · Official record ↗
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200 recalls
Official ID Z-2942-2026 · Official record ↗
Products may not have received adequate sterilization processing.
Company / brand: BD SWITZERLAND SARL recalls
Official ID Z-2941-2026 · Official record ↗
A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in CO2 leaking into the r…
Company / brand: Erbe USA recalls
Official ID Z-2938-2026 · Official record ↗
The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or inappropriate monitoring o…
Company / brand: Bioporto Diagnostics A/S recalls
Official ID Z-2937-2026 · Official record ↗
Due to increase in false negative results
Company / brand: BioFire Diagnostics recalls
Official ID Z-2936-2026 · Official record ↗
Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling would suggest…
Company / brand: Straumann USA recalls
Official ID Z-2935-2026 · Official record ↗
The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified s…
Company / brand: Waldemar Link & Co. KG (Mfg Site) recalls
Official ID Z-2934-2026 · Official record ↗
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the hea…
Company / brand: OBP Medical recalls
Official ID Z-2933-2026 · Official record ↗
Two software related issues: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2932-2026 · Official record ↗
Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropria…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2931-2026 · Official record ↗
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
Company / brand: Terumo Medical recalls
Official ID Z-2930-2026 · Official record ↗
There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the i…
Company / brand: Straumann USA recalls
Official ID Z-2929-2026 · Official record ↗
Firmware issue potentially leading to loss of geometry movements.
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2928-2026 · Official record ↗
Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.
Company / brand: Remel Europe recalls
Official ID Z-2927-2026 · Official record ↗
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life.…
Company / brand: Medline Industries recalls
Official ID Z-2926-2026 · Official record ↗
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life.…
Company / brand: Medline Industries recalls
Official ID Z-2925-2026 · Official record ↗
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life.…
Company / brand: Medline Industries recalls
Official ID Z-2924-2026 · Official record ↗
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life.…
Company / brand: Medline Industries recalls
Official ID Z-2923-2026 · Official record ↗
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v…
Company / brand: Covidien recalls
Official ID Z-2922-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.