Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 2,901–3,000, newest first.
Broken shock retainer bolt heads and washers may detach and become a road hazard, increasing the risk of a crash.
Company / brand: Lippert recalls
Official ID 26E032000 · Official record ↗
Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earl…
Company / brand: Medtronic Neuromodulation recalls
Official ID Z-2201-2026 · Official record ↗
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to …
Company / brand: MICROVENTION recalls
Official ID Z-2200-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2199-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2198-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2197-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2196-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2195-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2194-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2193-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2192-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2191-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2190-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2189-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2188-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2187-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2186-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2185-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2184-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2183-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2182-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2181-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2180-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2179-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2178-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2177-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2176-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2175-2026 · Official record ↗
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2174-2026 · Official record ↗
Out-of-specification endotoxin result that did not meet the acceptance criteria.
Company / brand: Integra LifeSciences (NeuroSciences) recalls
Official ID Z-2173-2026 · Official record ↗
Labeling update to provide warning if functionality of the valve replacement delivery system is compromised.
Company / brand: Edwards Lifesciences recalls
Official ID Z-2172-2026 · Official record ↗
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.
Company / brand: Aniara Diagnostica recalls
Official ID Z-2171-2026 · Official record ↗
Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to the forces …
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2170-2026 · Official record ↗
Product has the potential for false positive results
Company / brand: Quidel recalls
Official ID Z-2169-2026 · Official record ↗
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
Company / brand: Hologic recalls
Official ID Z-2168-2026 · Official record ↗
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
Company / brand: Hologic recalls
Official ID Z-2167-2026 · Official record ↗
Due to nonconforming products being inadvertently distributed.
Company / brand: Stryker recalls
Official ID Z-2166-2026 · Official record ↗
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app…
Company / brand: Dexcom recalls
Official ID Z-2165-2026 · Official record ↗
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app…
Company / brand: Dexcom recalls
Official ID Z-2164-2026 · Official record ↗
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app…
Company / brand: Dexcom recalls
Official ID Z-2163-2026 · Official record ↗
Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthri…
Company / brand: Technological Medical Advancements recalls
Official ID Z-2162-2026 · Official record ↗
Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service performed to justif…
Company / brand: Jolife AB recalls
Official ID Z-2161-2026 · Official record ↗
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Company / brand: ARROW INTERNATIONAL recalls
Official ID Z-2159-2026 · Official record ↗
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Company / brand: ARROW INTERNATIONAL recalls
Official ID Z-2158-2026 · Official record ↗
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Company / brand: ARROW INTERNATIONAL recalls
Official ID Z-2157-2026 · Official record ↗
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Company / brand: ARROW INTERNATIONAL recalls
Official ID Z-2156-2026 · Official record ↗
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2155-2026 · Official record ↗
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2154-2026 · Official record ↗
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2153-2026 · Official record ↗
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2152-2026 · Official record ↗
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2151-2026 · Official record ↗
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2150-2026 · Official record ↗
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2149-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2148-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2147-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2146-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2145-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2144-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2143-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2142-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2141-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2140-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2139-2026 · Official record ↗
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2138-2026 · Official record ↗
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Company / brand: DJO recalls
Official ID Z-2137-2026 · Official record ↗
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Company / brand: DJO recalls
Official ID Z-2136-2026 · Official record ↗
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Company / brand: DJO recalls
Official ID Z-2135-2026 · Official record ↗
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Company / brand: DJO recalls
Official ID Z-2134-2026 · Official record ↗
Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.
Company / brand: On-X Life Technologies recalls
Official ID Z-2133-2026 · Official record ↗
Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose …
Company / brand: Windstone Medical Packaging recalls
Official ID Z-2066-2026 · Official record ↗
Potential for mislabeled syringe produced by the i.v.STATION device.
Company / brand: Omnicell recalls
Official ID Z-2047-2026 · Official record ↗
Product has the potential to be contaminated with Salmonella.
Company / brand: Pure Ground Ingredients recalls
Official ID H-0853-2026 · Official record ↗
Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella.
Company / brand: Sugar Foods recalls
Official ID H-0781-2026 · Official record ↗
Undeclared allergen ingredient (fish)
Company / brand: Ocinet recalls
Official ID H-0780-2026 · Official record ↗
Products contain undeclared soy, specifically soy lecithin.
Company / brand: Prospector Popcorn recalls
Official ID H-0779-2026 · Official record ↗
Contains undeclared Blue 1
Company / brand: Raja Foods and Vegetables recalls
Official ID H-0778-2026 · Official record ↗
Contains undeclared FD&C Yellow 6
Company / brand: Raja Foods and Vegetables recalls
Official ID H-0777-2026 · Official record ↗
Contains undeclared allergens (cashews, milk, and soy).
Company / brand: WE R NUTS recalls
Official ID H-0775-2026 · Official record ↗
Undeclared allergens (wheat and soy).
Company / brand: Ferris Coffee and Nut Company recalls
Official ID H-0774-2026 · Official record ↗
Product may contain foreign objects, specifically glass.
Company / brand: FINESALER recalls
Official ID H-0773-2026 · Official record ↗
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0772-2026 · Official record ↗
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0771-2026 · Official record ↗
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0770-2026 · Official record ↗
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0769-2026 · Official record ↗
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0768-2026 · Official record ↗
Failed Dissolution Specifications
Company / brand: Ascend Laboratories recalls
Official ID D-0547-2026 · Official record ↗
Crystallization; identified as Buprenorphine free base
Company / brand: ENDO USA recalls
Official ID D-0527-2026 · Official record ↗
Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.
Company / brand: Oasis Medical recalls
Official ID D-0525-2026 · Official record ↗
Unexpected braking increases the risk of a crash.
Company / brand: Hyundai Motor America recalls
Official ID 26V316000 · Official record ↗
Missing weight information provided by the label may lead to unintentionally overloading the vehicle, increasing the risk of a crash.
Company / brand: Tesla recalls
Official ID 26V315000 · Official record ↗
A loss of vehicle control increases the risk of a crash.
Company / brand: Hyundai Motor America recalls
Official ID 26V314000 · Official record ↗
Inadequate rear lighting can reduce vehicle visibility or fail to alert other drivers when the vehicle is braking, turning, or reversing, increasing the risk of a crash.
Company / brand: Jerr-Dan recalls
Official ID 26E031000 · Official record ↗
Loose shock bolts may cause a loss of vehicle stability, increasing the risk of a crash.
Company / brand: Keystone RV Company recalls
Official ID 26V313000 · Official record ↗
An unsecured wheelchair can move during transit, increasing the risk of injury.
Company / brand: Endera Motors recalls
Official ID 26V312000 · Official record ↗
A loss of drive power can increase the risk of a crash.
Company / brand: Oshkosh recalls
Official ID 26V311000 · Official record ↗
Hydraulic functions that do not immediately stop when the ground level E-stop is pressed, increase the risk of injury.
Company / brand: Altec Industries recalls
Official ID 26V310000 · Official record ↗
Overheating in the HPCU increases the risk of a fire.
Company / brand: Hyundai Motor America recalls
Official ID 26V308000 · Official record ↗
An air bag inflator that ruptures may result in sharp metal fragments striking the driver or passengers, increasing the risk of injury or death.
Company / brand: Hyundai Motor America recalls
Official ID 26V307000 · Official record ↗
A rearview image that does not display correctly reduces the driver's view behind the vehicle, increasing the risk of a crash or injury.
Company / brand: Honda recalls
Official ID 26V306000 · Official record ↗
Corrosion on the electrical contacts may cause overheating, increasing the risk of a fire.
Company / brand: BMW Of North America recalls
Official ID 26V305000 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.