Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 1,401–1,500, newest first.
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability
Company / brand: Ascend Laboratories recalls
Official ID D-0739-2026 · Official record ↗
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability
Company / brand: Ascend Laboratories recalls
Official ID D-0738-2026 · Official record ↗
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability
Company / brand: Ascend Laboratories recalls
Official ID D-0737-2026 · Official record ↗
Presence of precipitate
Company / brand: MYLAN PHARMACEUTICALS recalls
Official ID D-0734-2026 · Official record ↗
CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received.
Company / brand: Glenmark Pharmaceuticals recalls
Official ID D-0731-2026 · Official record ↗
Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.
Company / brand: MICRO LABS USA recalls
Official ID D-0730-2026 · Official record ↗
An unlabeled ABS light may confuse following drivers, increasing the risk of a crash.
Company / brand: Wabash National recalls
Official ID 26V506000 · Official record ↗
The accumulation of exhaust fumes increases the risk of injury or death from carbon monoxide poisoning.
Company / brand: Escape Trailer Industries recalls
Official ID 26V505000 · Official record ↗
A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing …
Company / brand: Rosenbauer America recalls
Official ID 26V504000 · Official record ↗
A unprotected power feed wire increases the risk of a fire.
Company / brand: Forest River recalls
Official ID 26V503000 · Official record ↗
Insufficient low beam headlight illumination can reduce driver visibility, increasing the risk of a crash.
Company / brand: Daimler Trucks North America recalls
Official ID 26E052000 · Official record ↗
A dangling or completely disengaged solar panel may hit other vehicles or pedestrians, increasing the risk of a crash or injury.
Company / brand: Alamo Group recalls
Official ID 26V502000 · Official record ↗
A separated ABS ECU may become damaged, causing the ABS system to fail and increasing the risk of a crash.
Company / brand: Autocar recalls
Official ID 26V501000 · Official record ↗
A detached screw may lodge between the frame and stem, interfering with steering and increasing the risk of a crash or injury.
Company / brand: Honda recalls
Official ID 26V500000 · Official record ↗
The ladder may detach during use, increasing the risk of injury.
Company / brand: Brinkley RV recalls
Official ID 26V499000 · Official record ↗
People in an enclosed space, such as a garage, with a running generator may be at an increased risk of injury or death from carbon monoxide poisoning.
Company / brand: Winnebago Industries recalls
Official ID 26V498000 · Official record ↗
A fuel leak in the presence of an ignition source increases the risk of a fire.
Company / brand: Wanco recalls
Official ID 26V497000 · Official record ↗
A cracked wheel may lead to disc separation and a loss of control, increasing the risk of a crash.
Company / brand: General Motors recalls
Official ID 26V496000 · Official record ↗
An improperly installed seat belt buckle anchor may fail to properly restrain occupants, increasing the risk of injury during a crash.
Company / brand: Chrysler recalls
Official ID 26V495000 · Official record ↗
A loose component may move and damage the high voltage battery, increasing the risk of a fire.
Company / brand: General Motors recalls
Official ID 26V494000 · Official record ↗
An misfire or loss of drive power increases the risk of a crash.
Company / brand: Hyundai Motor America recalls
Official ID 26V493000 · Official record ↗
The lithium-ion battery in the recalled hand warmers can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards.
Company / brand: Shenzhen Street Cat Technology Co recalls
Official ID 26659 · Official notice ↗
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: Shenzhen Muqiqu Creative Development Co recalls
Official ID 26658 · Official notice ↗
The recalled baby loungers violate the mandatory safety standard for infant support cushions because the padding can obstruct an infant's breathing, posing a serious risk of injury…
Company / brand: Guangzhou Dida Electronic Commerce Co recalls
Official ID 26657 · Official notice ↗
The recalled doll playsets violate the small parts ban because the toys are for children under three years old and some of the accessories are small parts, posing a deadly choking …
Company / brand: Shantou Chenghai District Zhiwan Classroom Trading Co recalls
Official ID 26656 · Official notice ↗
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: Hangzhou Xinyanchuangxin Tech. Co recalls
Official ID 26655 · Official notice ↗
The recalled dive sticks violate the federal dive sticks ban because they exceeded the compress limit, posing an impalement hazard. In shallow water, children may fall or land on a…
Company / brand: Joyin US recalls
Official ID 26654 · Official notice ↗
The recalled fireworks rockets can explode prematurely before reaching their intended height, posing explosion and burn hazards.
Company / brand: Jake's Fireworks recalls
Official ID 26653 · Official notice ↗
The electrical cord on the recalled throws and blankets can detach and ignite, posing a risk of serious injury or death from fire, burn and shock hazards.
Company / brand: Hangzhouyuefangjiajuyongpinyouxiangongsi recalls
Official ID 26652 · Official notice ↗
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: HARPPA recalls
Official ID 26651 · Official notice ↗
The cups and containers violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed eas…
Company / brand: Golden Link recalls
Official ID 26650 · Official notice ↗
The recalled refrigerators' internal electrical components can short circuit and ignite, posing a risk of serious injury or death from fire and burn hazards.
Company / brand: Zhongshan Galanz recalls
Official ID 26649 · Official notice ↗
The recalled projectors' lithium-ion battery can overheat, posing a risk of serious injury or death from fire and burn hazards.
Company / brand: BenQ America recalls
Official ID 26647 · 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: Luoyang Siqi Trading Co recalls
Official ID 26646 · 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: Changzhou Jiaxuan Intelligence Furniture Co recalls
Official ID 26645 · Official notice ↗
The zipline kit's steel cable, turnbuckle and seat can detach or break during use, posing a fall hazard. The zipline spring brakes are not stiff enough to safely slow a rider down …
Company / brand: HuNanBoLuoDianZiShangWuYouXianGongSi D/B/A Trsmima or Hunan Pineapple Electronic Commerce Co recalls
Official ID 26632 · Official notice ↗
Improper air bag deployment can increase the risk of injury during a crash.
Company / brand: Toyota Motor Engineering & Manufacturing recalls
Official ID 26E051000 · Official record ↗
Improper air bag deployment can increase the risk of injury during a crash.
Company / brand: Toyota Motor Engineering & Manufacturing recalls
Official ID 26E050000 · Official record ↗
Due to an out-of-specification result for an unidentified impurity detected during routine stability testing.
Company / brand: Precision Dose recalls
Official ID EVT-99388-g6s9bf · Official record ↗
Failed Dissolution Specifications
Company / brand: Supernus Pharmaceuticals recalls
Official ID EVT-99375-1qlo6cy · Official record ↗
Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use, which could …
Company / brand: Karl Storz Endoscopy recalls
Official ID Z-2794-2026 · Official record ↗
Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as sys…
Company / brand: Alphatec Spine recalls
Official ID Z-2793-2026 · Official record ↗
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.
Company / brand: Medline Industries recalls
Official ID Z-2791-2026 · Official record ↗
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.
Company / brand: Medline Industries recalls
Official ID Z-2790-2026 · Official record ↗
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.
Company / brand: Medline Industries recalls
Official ID Z-2789-2026 · Official record ↗
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.
Company / brand: Medline Industries recalls
Official ID Z-2788-2026 · Official record ↗
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter…
Company / brand: Medline Industries recalls
Official ID Z-2787-2026 · Official record ↗
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter…
Company / brand: Medline Industries recalls
Official ID Z-2786-2026 · Official record ↗
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter…
Company / brand: Medline Industries recalls
Official ID Z-2785-2026 · Official record ↗
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter…
Company / brand: Medline Industries recalls
Official ID Z-2784-2026 · Official record ↗
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter…
Company / brand: Medline Industries recalls
Official ID Z-2783-2026 · Official record ↗
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter…
Company / brand: Medline Industries recalls
Official ID Z-2782-2026 · Official record ↗
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter…
Company / brand: Medline Industries recalls
Official ID Z-2781-2026 · Official record ↗
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter…
Company / brand: Medline Industries recalls
Official ID Z-2780-2026 · Official record ↗
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter…
Company / brand: Medline Industries recalls
Official ID Z-2779-2026 · Official record ↗
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts will not be t…
Company / brand: Medtronic MiniMed recalls
Official ID Z-2778-2026 · Official record ↗
Problem description/Reason for recall: During the period March 22, 2026, to May 29, 2026, recorded urination audio was captured at 48,000 Hz while the model was trained and validat…
Company / brand: Emano Metrics recalls
Official ID Z-2777-2026 · Official record ↗
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
Company / brand: Olympus of the Americas recalls
Official ID Z-2776-2026 · Official record ↗
The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully discharged into a low-power "shippin…
Company / brand: KENT IMAGING recalls
Official ID Z-2775-2026 · Official record ↗
Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants.
Company / brand: Micro Therapeutics recalls
Official ID Z-2774-2026 · Official record ↗
Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants.
Company / brand: Micro Therapeutics recalls
Official ID Z-2773-2026 · Official record ↗
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.
Company / brand: AVID Medical recalls
Official ID Z-2772-2026 · Official record ↗
Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more input. When a user modifies an inpu…
Company / brand: Boston Scientific recalls
Official ID Z-2771-2026 · Official record ↗
Due to manufacturing issues, reperfusion catheters may fractures
Company / brand: Penumbra recalls
Official ID Z-2770-2026 · Official record ↗
Due to device not having FDA Clearance
Company / brand: Prismatik Dentalcraft recalls
Official ID Z-2769-2026 · Official record ↗
Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices …
Company / brand: Medtronic Neurosurgery recalls
Official ID Z-2768-2026 · Official record ↗
User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to 34.4%) than the actual anatomical d…
Company / brand: PIE Medical Imaging B.V recalls
Official ID Z-2767-2026 · Official record ↗
The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that co…
Company / brand: Medline Industries recalls
Official ID Z-2765-2026 · Official record ↗
The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that co…
Company / brand: Medline Industries recalls
Official ID Z-2764-2026 · Official record ↗
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Company / brand: AVID Medical recalls
Official ID Z-2763-2026 · Official record ↗
Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
Company / brand: SEASPINE ORTHOPEDICS recalls
Official ID Z-2762-2026 · Official record ↗
Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.
Company / brand: Olympus of the Americas recalls
Official ID Z-2761-2026 · Official record ↗
Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case condition, rail mechanism may b…
Company / brand: Ferno-Washington recalls
Official ID Z-2760-2026 · Official record ↗
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent application at the tubing t…
Company / brand: ICU Medical recalls
Official ID Z-2759-2026 · Official record ↗
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.
Company / brand: Paragon 28 recalls
Official ID Z-2758-2026 · Official record ↗
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orient…
Company / brand: Boston Scientific recalls
Official ID Z-2757-2026 · Official record ↗
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orient…
Company / brand: Boston Scientific recalls
Official ID Z-2756-2026 · Official record ↗
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orient…
Company / brand: Boston Scientific recalls
Official ID Z-2755-2026 · Official record ↗
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orient…
Company / brand: Boston Scientific recalls
Official ID Z-2754-2026 · Official record ↗
Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter.
Company / brand: Boston Scientific recalls
Official ID Z-2753-2026 · Official record ↗
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.
Company / brand: Boston Scientific recalls
Official ID Z-2752-2026 · Official record ↗
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.
Company / brand: Boston Scientific recalls
Official ID Z-2751-2026 · Official record ↗
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.
Company / brand: Boston Scientific recalls
Official ID Z-2750-2026 · Official record ↗
Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Brau…
Company / brand: Medline Industries recalls
Official ID Z-2749-2026 · Official record ↗
Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Brau…
Company / brand: Medline Industries recalls
Official ID Z-2748-2026 · Official record ↗
Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Brau…
Company / brand: Medline Industries recalls
Official ID Z-2747-2026 · Official record ↗
Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all units should be retu…
Company / brand: Wilcox Industries recalls
Official ID Z-2675-2026 · Official record ↗
No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6.
Company / brand: Man Fon recalls
Official ID H-1188-2026 · Official record ↗
Undeclared colors: Yellow#5, and Yellow#6.
Company / brand: Man Fon recalls
Official ID H-1187-2026 · Official record ↗
Undeclared Allergen (Fish)
Company / brand: GELLERT GLOBAL GROUP recalls
Official ID H-1186-2026 · Official record ↗
Contaminated with Salmonella
Company / brand: Total Nutrition recalls
Official ID H-1185-2026 · Official record ↗
Undeclared sodium tripolyphosphate (STTP)
Company / brand: Shandong Ling Xian Food Co recalls
Official ID H-1184-2026 · Official record ↗
Undeclared sodium tripolyphosphate (STTP)
Company / brand: Shandong Ling Xian Food Co recalls
Official ID H-1183-2026 · Official record ↗
Undeclared sodium tripolyphosphate (STTP)
Company / brand: Shandong Ling Xian Food Co recalls
Official ID H-1182-2026 · Official record ↗
Moringa Powder ingredient positive for salmonella
Company / brand: Green Jeeva recalls
Official ID H-1180-2026 · Official record ↗
Ambient storage of the product may lead to Clostridium botulinum toxin formation.
Company / brand: Brooklyn Roasting Works recalls
Official ID H-1179-2026 · Official record ↗
FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
Company / brand: Modern Warrior Life recalls
Official ID H-1178-2026 · Official record ↗
Unapproved food additive: sassafras bark.
Company / brand: Vintage Roots recalls
Official ID H-1177-2026 · Official record ↗
Failed Dissolution Specifications
Company / brand: Supernus Pharmaceuticals recalls
Official ID D-0758-2026 · Official record ↗
Presence of Foreign Tablets/Capsules
Company / brand: Bionpharma recalls
Official ID D-0742-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.