Latest recalls — page 17
Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 1,601–1,700, newest first.
FDA Class I · Medical device · July 22, 2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2689-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2688-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2687-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2686-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2685-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2684-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2683-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2682-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2681-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub …
Company / brand: Oscor recalls
Official ID Z-2680-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub …
Company / brand: Oscor recalls
Official ID Z-2679-2026 ·
Official record ↗
FDA Class I · Medical device · July 22, 2026
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub …
Company / brand: Oscor recalls
Official ID Z-2678-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
Potential E. coli O145:H28 Contamination
Company / brand: Frutas y Hortalizas del Sur recalls
Official ID H-1181-2026 ·
Official record ↗
FDA Class II · Food · July 22, 2026
Foreign material (Glass) was found in the product.
Company / brand: GELLERT GLOBAL GROUP recalls
Official ID H-1176-2026 ·
Official record ↗
FDA Class II · Food · July 22, 2026
Undeclared peanuts
Company / brand: Fayus recalls
Official ID H-1175-2026 ·
Official record ↗
FDA Class II · Food · July 22, 2026
Potential for spoilage.
Company / brand: AMY'S KITCHEN recalls
Official ID H-1174-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1173-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1172-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1171-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1170-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1169-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1168-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1167-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1166-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1165-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1164-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1163-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1162-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1161-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1160-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1159-2026 ·
Official record ↗
FDA Class I · Food · July 22, 2026
May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Company / brand: D'Dioses Fruit Pops recalls
Official ID H-1158-2026 ·
Official record ↗
FDA Class II · Food · July 22, 2026
Product may contain metal fragments.
Company / brand: W.Y. Industries recalls
Official ID H-1157-2026 ·
Official record ↗
FDA Class II · Food · July 22, 2026
Undeclared milk allergen.
Company / brand: Chocolate Bar Holdings recalls
Official ID H-1156-2026 ·
Official record ↗
FDA Class II · Food · July 22, 2026
Potential foreign material (glass)
Company / brand: General Mills James Ford Bell Technical Center recalls
Official ID H-1155-2026 ·
Official record ↗
FDA Class II · Food · July 22, 2026
Potential foreign material (glass)
Company / brand: General Mills James Ford Bell Technical Center recalls
Official ID H-1154-2026 ·
Official record ↗
FDA Class II · Food · July 22, 2026
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A…
Company / brand: Nutricia North America recalls
Official ID H-1153-2026 ·
Official record ↗
FDA Class II · Food · July 22, 2026
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A…
Company / brand: Nutricia North America recalls
Official ID H-1152-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator
Company / brand: CareFusion 213 recalls
Official ID D-0690-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
Lack of Assurance of Sterility
Company / brand: Chiesi USA recalls
Official ID D-0689-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0688-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0687-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0686-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0685-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0684-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0683-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0682-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0681-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0680-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0679-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Company / brand: Bell Pharmaceuticals recalls
Official ID D-0678-2026 ·
Official record ↗
FDA Class II · Drug · July 22, 2026
Subpotent Drug: Low out of specification assay results performed during long-term stability testing.
Company / brand: Padagis US recalls
Official ID D-0677-2026 ·
Official record ↗
NHTSA · Vehicle · July 21, 2026
Unexpected movement of the driver’s seat back may trap a second-row occupant, increasing the risk of injury.
Company / brand: Ford Motor Company recalls
Official ID 26V470000 ·
Official record ↗
NHTSA · Vehicle · July 21, 2026
An incorrect VIN on the label can make it difficult for owners to recognize that their vehicle is involved in a safety recall, increasing the risk of crash or injury.
Company / brand: Ember Recreational Vehicles recalls
Official ID 26V469000 ·
Official record ↗
NHTSA · Vehicle · July 20, 2026
A short circuit in the engine compartment can create heat or spark, increasing the risk of a fire.
Company / brand: Ford Motor Company recalls
Official ID 26V468000 ·
Official record ↗
NHTSA · Vehicle · July 20, 2026
A brake fluid leak in the presence of an ignition source such as hot engine or exhaust components can increase the risk of a fire. Additionally, a brake fluid leak can extend the d…
Company / brand: Blue Bird Body Company recalls
Official ID 26V467000 ·
Official record ↗
NHTSA · Vehicle · July 20, 2026
A brake fluid leak in the presence of an ignition source such as hot engine or exhaust components can increase the risk of a fire. Additionally, a brake fluid leak can extend the d…
Company / brand: Blue Bird Body Company recalls
Official ID 26V466000 ·
Official record ↗
NHTSA · Vehicle · July 17, 2026
A rear impact guard that is not properly installed can increase the risk of injury during a crash.
Company / brand: Great Dane Trailers recalls
Official ID 26V465000 ·
Official record ↗
NHTSA · Vehicle · July 17, 2026
An overheated printed circuit board increases the risk of a fire.
Company / brand: Foretravel recalls
Official ID 26V464000 ·
Official record ↗
NHTSA · Vehicle · July 17, 2026
A fastener that has not been heat treated could fail, resulting in separation of the pedestal and turntable, increasing the risk of injury.
Company / brand: Altec Industries recalls
Official ID 26V463000 ·
Official record ↗
NHTSA · Vehicle · July 17, 2026
A wheelchair lift that continues to move while occupied increases the risk of injury.
Company / brand: Turtle Top recalls
Official ID 26V462000 ·
Official record ↗
NHTSA · Child car seat · July 17, 2026
A headrest that shifts unexpectedly may increase the risk of injury in a crash.
Company / brand: Evenflo Company recalls
Official ID 26C004000 ·
Official record ↗
NHTSA · Vehicle · July 16, 2026
The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.
Company / brand: International Motors recalls
Official ID 26V461000 ·
Official record ↗
NHTSA · Vehicle · July 16, 2026
The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.
Company / brand: International Motors recalls
Official ID 26V460000 ·
Official record ↗
NHTSA · Vehicle · July 16, 2026
A short circuit increases the risk of a fire.
Company / brand: International Motors recalls
Official ID 26V459000 ·
Official record ↗
NHTSA · Vehicle · July 16, 2026
A rearview camera image that does not display can decrease the driver's visibility, increasing the risk of a crash.
Company / brand: Jaguar Land Rover North America recalls
Official ID 26V458000 ·
Official record ↗
NHTSA · Vehicle · July 16, 2026
An overheated wire can ignite flammable material in the cargo area, increasing the risk of fire.
Company / brand: Altec Industries recalls
Official ID 26V457000 ·
Official record ↗
NHTSA · Vehicle · July 16, 2026
Loss of vehicle control increases the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26V456000 ·
Official record ↗
CPSC · Consumer Product · July 16, 2026
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: Zhuzhoushizuisuanshangmaoyouxiangongsi recalls
Official ID 26630 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard.
Company / brand: Target recalls
Official ID 26629 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and d…
Company / brand: Yiwushi Bihe Trading Co recalls
Official ID 26628 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
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: Dongguan Shinneng Huizheng Network Technology Co recalls
Official ID 26627 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of serious injury or dea…
Company / brand: Madewell recalls
Official ID 26626 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death.
Company / brand: J. Crew Group recalls
Official ID 26625 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning.
Company / brand: Huish Outdoors recalls
Official ID 26624 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or children and can cau…
Company / brand: Warren James recalls
Official ID 26623 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
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: Wuxi Leclaire Home Products Co recalls
Official ID 26622 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The recalled chandeliers lack proper electrical grounding, posing a risk of serious injury or death from electrocution hazard.
Company / brand: Currey & Company recalls
Official ID 26621 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The recalled toddler towers can tip over while in use, posing a risk of serious injury and death, due to tip over and fall hazards.
Company / brand: TOMY International recalls
Official ID 26620 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottles are not …
Company / brand: Shenzhen Gudebo Technology Co recalls
Official ID 26619 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard.
Company / brand: Panasonic Manufacturing (Xiamen) Co recalls
Official ID 26618 ·
Official notice ↗
CPSC · Consumer Product · July 16, 2026
The recalled finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or coin…
Company / brand: Shenzhen Dami Trading Co recalls
Official ID 26617 ·
Official notice ↗
NHTSA · Vehicle · July 15, 2026
An overloaded vehicle can increase the risk of a crash.
Company / brand: Nissan North America recalls
Official ID 26V455000 ·
Official record ↗
NHTSA · Vehicle · July 15, 2026
Loss of power to the rear wheels can prevent the vehicle from moving, increasing the risk of a crash.
Company / brand: E-One Incorporated recalls
Official ID 26V454000 ·
Official record ↗
NHTSA · Vehicle · July 15, 2026
A detached rail can cause a loss of control, increasing the risk of injury.
Company / brand: Orange EV recalls
Official ID 26V453000 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk.
Company / brand: CMR SURGICAL recalls
Official ID Z-2717-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
Company / brand: Think Surgical recalls
Official ID Z-2716-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.
Company / brand: Biomerieux recalls
Official ID Z-2715-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 …
Company / brand: Integra LifeSciences (NeuroSciences) recalls
Official ID Z-2714-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.
Company / brand: WALLAC OY recalls
Official ID Z-2713-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
Company / brand: Elekta recalls
Official ID Z-2712-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
Company / brand: Elekta recalls
Official ID Z-2711-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
Company / brand: Elekta recalls
Official ID Z-2710-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated HbA1c patien…
Company / brand: Siemens Healthcare Diagnostics recalls
Official ID Z-2703-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem.
Company / brand: Fresenius Medical Care Holdings recalls
Official ID Z-2702-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Due to packaging discrepancy with incorrect product size mixed up.
Company / brand: Encore Medical recalls
Official ID Z-2701-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
Due to packaging discrepancy with incorrect product size mixed up.
Company / brand: Encore Medical recalls
Official ID Z-2700-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
A product error defect may cause incorrect bracket placement.
Company / brand: Klowen Braces recalls
Official ID Z-2699-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error me…
Company / brand: Medtronic MiniMed recalls
Official ID Z-2698-2026 ·
Official record ↗
FDA Class II · Medical device · July 15, 2026
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-2697-2026 ·
Official record ↗
Official sources
Government sources last checked October 22, 2026 at 12:00 PM UTC.