Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 101–200, newest first.
Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0025-2027 · Official record ↗
Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0024-2027 · Official record ↗
Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0023-2027 · Official record ↗
Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0022-2027 · Official record ↗
Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0021-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0020-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0019-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0018-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0017-2027 · Official record ↗
Presence of particulate matter.
Company / brand: J&J INNOVATIVE MEDICINE recalls
Official ID D-0016-2027 · Official record ↗
Failed Impurities/Degradation Specifications
Company / brand: Cipla USA recalls
Official ID D-0014-2027 · Official record ↗
Failed Content Uniformity Specifications
Company / brand: Preferred Pharmaceuticals recalls
Official ID D-0013-2027 · Official record ↗
Failed stability specifications
Company / brand: BioSpectra recalls
Official ID D-0012-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: K.C. Pharmaceuticals recalls
Official ID D-0009-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: K.C. Pharmaceuticals recalls
Official ID D-0008-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: K.C. Pharmaceuticals recalls
Official ID D-0007-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: K.C. Pharmaceuticals recalls
Official ID D-0006-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: K.C. Pharmaceuticals recalls
Official ID D-0005-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: K.C. Pharmaceuticals recalls
Official ID D-0004-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: K.C. Pharmaceuticals recalls
Official ID D-0003-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: K.C. Pharmaceuticals recalls
Official ID D-0002-2027 · Official record ↗
An unprotected charge line can cause the wire to overheat, increasing the risk of a fire.
Company / brand: K.Z recalls
Official ID 26V672000 · Official record ↗
A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.
Company / brand: Temsa recalls
Official ID 26V669000 · Official record ↗
A detached head restraint cushion can increase the risk of injury during a crash.
Company / brand: Volvo Car Usa recalls
Official ID 26V671000 · Official record ↗
Referencing incorrect information can result in installing the wrong size replacement tires or underinflating the tires, increasing the risk of a crash.
Company / brand: Grand Design RV recalls
Official ID 26V668000 · Official record ↗
Underrated chains can allow the trailer to detach from the tow vehicle, increasing the risk of a crash.
Company / brand: Grand Design RV recalls
Official ID 26V667000 · Official record ↗
A missing rearview camera can reduce the driver's view behind the vehicle, increasing the risk of a crash.
Company / brand: Altec Industries recalls
Official ID 26V666000 · Official record ↗
A front bumper that detaches can become a road hazard and increase the risk of a crash. In addition, the bolts can fail suddenly during winch operation, increasing the risk of inju…
Company / brand: Altec Industries recalls
Official ID 26V665000 · Official record ↗
A fire increases the risk of injury.
Company / brand: Hyundai Motor America recalls
Official ID 26V664000 · Official record ↗
In the event of a short circuit, inadequate protection increases the risk of a fire.
Company / brand: Lippert recalls
Official ID 26E070000 · Official record ↗
A detached bottle cap can become a projectile and strike the user or others nearby, increasing the risk of injury.
Company / brand: Honda recalls
Official ID 26V663000 · Official record ↗
A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.
Company / brand: Tiffin Motorhomes recalls
Official ID 26V662000 · Official record ↗
A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.
Company / brand: Sutphen recalls
Official ID 26V661000 · Official record ↗
The recalled medals violate the mandatory safety standard for magnets because the high-powered magnets may detach, posing a deadly ingestion hazard to children. When high-powered m…
Company / brand: Actionary recalls
Official ID 27022 · Official notice ↗
The fireplace's lava rocks can ignite and explode when heated in the propane insert, posing a risk of serious injury or death from burn and fire hazards.
Company / brand: Snow Peak USA recalls
Official ID 27021 · Official notice ↗
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. T…
Company / brand: Zhangzhou Jinhao Sen Smart Home Co recalls
Official ID 27020 · Official notice ↗
The seats, metal carabiners or quick links, or webbing straps of the recalled swing seats can break during use, posing a risk of serious injury due to fall hazard.
Company / brand: Pacearth Direct recalls
Official ID 27019 · Official notice ↗
The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due t…
Company / brand: Hubei Youhong Trading Co recalls
Official ID 27018 · Official notice ↗
The recalled bicycles' front lock nut can loosen during use, causing the front wheel to dislodge or loosen over time, posing a crash hazard.
Company / brand: Decathlon America recalls
Official ID 27017 · Official notice ↗
Grass and debris can accumulate in the trimmer mowers and ignite, posing a risk of serious injury or death from fire and burn hazards.
Company / brand: Generac Power Systems recalls
Official ID 27016 · Official notice ↗
The LED-light key that was included with certain SureLock Bicycle Lock sets violates the mandatory safety standard for consumer products with button cell and coin batteries because…
Company / brand: Giant Bicycle recalls
Official ID 27015 · Official notice ↗
A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.
Company / brand: Daimler Trucks North America recalls
Official ID 26V660000 · Official record ↗
An unexpected powertrain shutdown can cause a loss of drive power, increasing the risk of a crash.
Company / brand: Toyota Motor Engineering & Manufacturing recalls
Official ID 26V659000 · Official record ↗
An overheated reverse gear control unit increases the risk of a fire.
Company / brand: BMW Of North America recalls
Official ID 26V658000 · Official record ↗
Discoloration: consumer complaints received for discolored tablets
Company / brand: Aurobindo Pharma USA recalls
Official ID EVT-99934-1f1l4x9 · Official record ↗
The potential for falsely elevated results.
Company / brand: Siemens Healthcare Diagnostics recalls
Official ID Z-3335-2026 · Official record ↗
Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads, which if used would preve…
Company / brand: Wright Medical Technology recalls
Official ID Z-3334-2026 · Official record ↗
Due to incorrect inside packaging label for eyepiece.
Company / brand: Karl Storz Endoscopy recalls
Official ID Z-3333-2026 · Official record ↗
Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may output the message System Stopped By Fatal Error: DBConnectionError AlarmDB when launching the …
Company / brand: Beckman Coulter Mishima K.K recalls
Official ID Z-3332-2026 · Official record ↗
Due to manufacturing issues reperfusion catheters may fracture.
Company / brand: Penumbra recalls
Official ID Z-3331-2026 · Official record ↗
A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a software issue preventing successful pairing of the t:slim application with Abbott FreeStyle …
Company / brand: Tandem Diabetes Care recalls
Official ID Z-3330-2026 · Official record ↗
While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.
Company / brand: Olympus of the Americas recalls
Official ID Z-3329-2026 · Official record ↗
Due to blood-to-glycol leak in the heat exchanger.
Company / brand: SPECTRUM MEDICAL SRL recalls
Official ID Z-3328-2026 · Official record ↗
Due to blood-to-glycol leak in the heat exchanger.
Company / brand: SPECTRUM MEDICAL SRL recalls
Official ID Z-3327-2026 · Official record ↗
Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter.
Company / brand: Micro Therapeutics recalls
Official ID Z-3326-2026 · Official record ↗
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o…
Company / brand: Percussionaire recalls
Official ID Z-3325-2026 · Official record ↗
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o…
Company / brand: Percussionaire recalls
Official ID Z-3324-2026 · Official record ↗
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o…
Company / brand: Percussionaire recalls
Official ID Z-3323-2026 · Official record ↗
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o…
Company / brand: Percussionaire recalls
Official ID Z-3322-2026 · Official record ↗
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o…
Company / brand: Percussionaire recalls
Official ID Z-3321-2026 · Official record ↗
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o…
Company / brand: Percussionaire recalls
Official ID Z-3320-2026 · Official record ↗
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o…
Company / brand: Percussionaire recalls
Official ID Z-3319-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3318-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3317-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3316-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3315-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3314-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3313-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3312-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3311-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3310-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3309-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3308-2026 · Official record ↗
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced …
Company / brand: Philips North America recalls
Official ID Z-3307-2026 · Official record ↗
Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors.
Company / brand: NOXBOX recalls
Official ID Z-3306-2026 · Official record ↗
Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the sterile barrier, whi…
Company / brand: Merit Medical Systems recalls
Official ID Z-3305-2026 · Official record ↗
Potential for monomer liquid leakage.
Company / brand: Heraeus Medical (Dental Division) recalls
Official ID Z-3304-2026 · Official record ↗
Potential for monomer liquid leakage.
Company / brand: Heraeus Medical (Dental Division) recalls
Official ID Z-3303-2026 · Official record ↗
Potential for monomer liquid leakage.
Company / brand: Heraeus Medical (Dental Division) recalls
Official ID Z-3302-2026 · Official record ↗
Potential for monomer liquid leakage.
Company / brand: Heraeus Medical (Dental Division) recalls
Official ID Z-3301-2026 · Official record ↗
There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese package insert.
Company / brand: Olympus of the Americas recalls
Official ID Z-3300-2026 · Official record ↗
There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese package insert.
Company / brand: Olympus of the Americas recalls
Official ID Z-3299-2026 · Official record ↗
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the fl…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3298-2026 · Official record ↗
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the fl…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3297-2026 · Official record ↗
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the fl…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3296-2026 · Official record ↗
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the fl…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3295-2026 · Official record ↗
Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. U…
Company / brand: American Contract Systems recalls
Official ID Z-3294-2026 · Official record ↗
Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. U…
Company / brand: American Contract Systems recalls
Official ID Z-3293-2026 · Official record ↗
Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. U…
Company / brand: American Contract Systems recalls
Official ID Z-3292-2026 · Official record ↗
Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading…
Company / brand: American Nitrile Operations recalls
Official ID Z-3291-2026 · Official record ↗
Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading…
Company / brand: American Nitrile Operations recalls
Official ID Z-3290-2026 · Official record ↗
Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading…
Company / brand: American Nitrile Operations recalls
Official ID Z-3289-2026 · Official record ↗
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …
Company / brand: Shanghai United Imaging Healthcare Co recalls
Official ID Z-3288-2026 · Official record ↗
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …
Company / brand: Shanghai United Imaging Healthcare Co recalls
Official ID Z-3287-2026 · Official record ↗
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …
Company / brand: Shanghai United Imaging Healthcare Co recalls
Official ID Z-3286-2026 · Official record ↗
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …
Company / brand: Shanghai United Imaging Healthcare Co recalls
Official ID Z-3285-2026 · Official record ↗
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …
Company / brand: Shanghai United Imaging Healthcare Co recalls
Official ID Z-3284-2026 · Official record ↗
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …
Company / brand: Shanghai United Imaging Healthcare Co recalls
Official ID Z-3283-2026 · Official record ↗
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …
Company / brand: Shanghai United Imaging Healthcare Co recalls
Official ID Z-3282-2026 · Official record ↗
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single …
Company / brand: Shanghai United Imaging Healthcare Co recalls
Official ID Z-3281-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.