Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 1,701–1,800, newest first.
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm ge…
Company / brand: Medline Industries recalls
Official ID Z-2696-2026 · Official record ↗
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm ge…
Company / brand: Medline Industries recalls
Official ID Z-2695-2026 · Official record ↗
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to…
Company / brand: Boston Scientific Neuromodulation recalls
Official ID Z-2694-2026 · Official record ↗
Surgical dressing manufactured out of specification (greater thickness).
Company / brand: ConvaTec recalls
Official ID Z-2677-2026 · Official record ↗
Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers.
Company / brand: Olympus of the Americas recalls
Official ID Z-2676-2026 · Official record ↗
Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging.
Company / brand: Lehi Valley Trading Company recalls
Official ID H-1150-2026 · Official record ↗
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the pote…
Company / brand: Fresh & Ready Foods recalls
Official ID H-1149-2026 · Official record ↗
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due …
Company / brand: Fresh & Ready Foods recalls
Official ID H-1148-2026 · Official record ↗
Foreign material: small metal pieces
Company / brand: Wondermade recalls
Official ID H-1147-2026 · Official record ↗
The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.
Company / brand: Wise Foods recalls
Official ID H-1146-2026 · Official record ↗
Undeclared Allergen (Soy)
Company / brand: Specialty Bakers recalls
Official ID H-1145-2026 · Official record ↗
Potential contamination with Salmonella
Company / brand: Trafa Pharmaceutical recalls
Official ID H-1144-2026 · Official record ↗
undeclared soy
Company / brand: Bear Stewart Co recalls
Official ID H-1143-2026 · Official record ↗
Undeclared Sesame allergen
Company / brand: Adams Extract & Spice recalls
Official ID H-1142-2026 · Official record ↗
Undeclared Sesame allergen
Company / brand: Adams Extract & Spice recalls
Official ID H-1141-2026 · Official record ↗
Undeclared Sesame allergen
Company / brand: Adams Extract & Spice recalls
Official ID H-1140-2026 · Official record ↗
Undeclared Sesame allergen
Company / brand: Adams Extract & Spice recalls
Official ID H-1139-2026 · Official record ↗
Undeclared Sesame allergen
Company / brand: Adams Extract & Spice recalls
Official ID H-1138-2026 · Official record ↗
cGMP deviations
Company / brand: Shimoga Chemicals recalls
Official ID D-0691-2026 · Official record ↗
Lack of Sterility Assurance
Company / brand: Reliance Life Sciences Private recalls
Official ID D-0674-2026 · Official record ↗
Lack of Sterility Assurance
Company / brand: Reliance Life Sciences Private recalls
Official ID D-0673-2026 · Official record ↗
Lack of Sterility Assurance
Company / brand: Reliance Life Sciences Private recalls
Official ID D-0672-2026 · Official record ↗
Lack of Sterility Assurance
Company / brand: Reliance Life Sciences Private recalls
Official ID D-0671-2026 · Official record ↗
Subpotent drug
Company / brand: Gasco Industrial recalls
Official ID D-0670-2026 · Official record ↗
Subpotent drug
Company / brand: Gasco Industrial recalls
Official ID D-0669-2026 · Official record ↗
Subpotent drug
Company / brand: Gasco Industrial recalls
Official ID D-0668-2026 · Official record ↗
Subpotent drug
Company / brand: Gasco Industrial recalls
Official ID D-0667-2026 · Official record ↗
Subpotent drug
Company / brand: Gasco Industrial recalls
Official ID D-0666-2026 · Official record ↗
Subpotent drug
Company / brand: Gasco Industrial recalls
Official ID D-0665-2026 · Official record ↗
Failed Impurities/Degradation Specifications
Company / brand: QuVa Pharma recalls
Official ID D-0664-2026 · Official record ↗
Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification.
Company / brand: BioMed Laboratories recalls
Official ID D-0663-2026 · Official record ↗
Failed Impurities/Degradation Specifications
Company / brand: ONESOURCE SPECIALTY PHARMA recalls
Official ID D-0662-2026 · Official record ↗
A seat belt buckle that fails to properly restrain an occupant in a crash increases the risk of injury.
Company / brand: Hyundai Motor America recalls
Official ID 26V452000 · Official record ↗
A seat that moves unexpectedly may not properly restrain an occupant during a crash, increasing the risk of injury.
Company / brand: Ford Motor Company recalls
Official ID 26V451000 · Official record ↗
An overheated printed circuit board increases the risk of a fire.
Company / brand: Winnebago Industries recalls
Official ID 26V450000 · Official record ↗
A liftgate that falls unexpectedly increases the risk of injury.
Company / brand: Wabash National recalls
Official ID 26V449000 · Official record ↗
A detached roof rail cover can create a road hazard, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V448000 · Official record ↗
A loss of trailer brakes or lights can reduce the driver’s ability to control the trailer and decrease the trailers visibility to other road users, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26E046000 · Official record ↗
An overheated printed circuit board increases the risk of a fire.
Company / brand: Grand Design RV recalls
Official ID 26V446000 · Official record ↗
A loss of steering increases the risk of a crash.
Company / brand: Tenneco Automotive recalls
Official ID 26E045000 · Official record ↗
Failing to respond to low visibility conditions can increase the risk of a crash or impede first responders.
Company / brand: Zoox recalls
Official ID 26E044000 · Official record ↗
A loose steering arm can result in a loss of vehicle steering control, increasing the risk of a crash.
Company / brand: Volvo Trucks North America recalls
Official ID 26V444000 · Official record ↗
Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit, posing a risk of serio…
Company / brand: Greenworks North America recalls
Official ID 26611 · Official notice ↗
The lithium-ion battery in the recalled power banks (chargers) can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards.
Company / brand: iDecoz dba Flaunt recalls
Official ID 26610 · Official notice ↗
The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk …
Company / brand: Zhangzhoushi Jingqu Trading Co recalls
Official ID 26609 · Official notice ↗
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of th…
Company / brand: shenzhenshiyuezhangwangluokejiyouxiangongsi (Shenzhen Yuezhang Network Technology Co recalls
Official ID 26608 · Official notice ↗
The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
Company / brand: Jomani International recalls
Official ID 26607 · Official notice ↗
The recalled ranges' front-mounted knobs can be activated accidentally by humans or pets, posing a risk of serious injury from a fire hazard.
Company / brand: Best Buy Purchasing recalls
Official ID 26606 · Official notice ↗
The tempered glass window in the pizza oven can shatter during use, posing a risk of serious injury from laceration hazard.
Company / brand: Conair recalls
Official ID 26605 · Official notice ↗
Cracks or breaks in the rear brake caliper can reduce braking ability, increasing the risk of a crash.
Company / brand: KTM North America recalls
Official ID 26V443000 · Official record ↗
An incorrectly installed quick release valve that does not function properly can increase the risk of a crash.
Company / brand: Paccar Incorporated recalls
Official ID 26V442000 · Official record ↗
A short circuit in the starter relay may increase the risk of a fire.
Company / brand: BMW Of North America recalls
Official ID 26V441000 · Official record ↗
An electrical short increases the risk of a fire.
Company / brand: SHYFT Group recalls
Official ID 26V440000 · Official record ↗
Referencing the incorrect GVWR may lead to unintentionally overloading the vehicle, increasing the risk of a crash.
Company / brand: Forest River recalls
Official ID 26V439000 · Official record ↗
Fire increases the risk of injury.
Company / brand: BMW Of North America recalls
Official ID 26V438000 · Official record ↗
A broken rear axle carrier can cause a sudden loss of vehicle stability and control, increasing the risk of a crash.
Company / brand: Toyota Motor Engineering & Manufacturing recalls
Official ID 26V437000 · Official record ↗
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
Company / brand: Lupin Pharmaceuticals recalls
Official ID EVT-99296-c9qbin · Official record ↗
undeclared colors (yellow#5)
Company / brand: Le Chef Bakery recalls
Official ID EVT-99205-115w1r1 · Official record ↗
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insigni…
Company / brand: Zimmer Surgical recalls
Official ID Z-2674-2026 · Official record ↗
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insigni…
Company / brand: Zimmer Surgical recalls
Official ID Z-2673-2026 · Official record ↗
Due to catheter separation
Company / brand: W L Gore & Associates recalls
Official ID Z-2672-2026 · Official record ↗
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate pati…
Company / brand: Masimo recalls
Official ID Z-2671-2026 · Official record ↗
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate pati…
Company / brand: Masimo recalls
Official ID Z-2670-2026 · Official record ↗
Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the h…
Company / brand: Laborie Medical Technologies recalls
Official ID Z-2669-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2668-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2667-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2666-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2665-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2664-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2663-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2662-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2661-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2660-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2659-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2658-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2657-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2656-2026 · Official record ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Company / brand: Bard Access Systems recalls
Official ID Z-2655-2026 · Official record ↗
Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
Company / brand: BD SWITZERLAND SARL recalls
Official ID Z-2654-2026 · Official record ↗
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.
Company / brand: Covidien recalls
Official ID Z-2653-2026 · Official record ↗
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
Company / brand: Carl Zeiss Meditec AG recalls
Official ID Z-2649-2026 · Official record ↗
Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws that keep the monitor attached to the suspension may gradual…
Company / brand: Siemens Medical Solutions USA recalls
Official ID Z-2648-2026 · Official record ↗
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session,…
Company / brand: RAYSEARCH LABORATORIES AB recalls
Official ID Z-2647-2026 · Official record ↗
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session,…
Company / brand: RAYSEARCH LABORATORIES AB recalls
Official ID Z-2646-2026 · Official record ↗
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritiona…
Company / brand: Medela recalls
Official ID Z-2645-2026 · Official record ↗
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and i…
Company / brand: Accuray Incorporated recalls
Official ID Z-2644-2026 · Official record ↗
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
Company / brand: Siemens Medical Solutions USA recalls
Official ID Z-2643-2026 · Official record ↗
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
Company / brand: Siemens Medical Solutions USA recalls
Official ID Z-2642-2026 · Official record ↗
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
Company / brand: Siemens Medical Solutions USA recalls
Official ID Z-2641-2026 · Official record ↗
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and i…
Company / brand: Accuray Incorporated recalls
Official ID Z-2640-2026 · Official record ↗
Due to out-of-specification, or potential out-of-specification, levels of endotoxins
Company / brand: TELEFLEX recalls
Official ID Z-2639-2026 · Official record ↗
The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of the Upper Back Secti…
Company / brand: Baxter Healthcare recalls
Official ID Z-2638-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2637-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2636-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2635-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2634-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2633-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2632-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2631-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2630-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.