Alaska recalls
1,901 federal recalls affecting Alaska in the last 12 months: 27 sold in Alaska plus 1,874 sold nationwide. From the CPSC, FDA, USDA and NHTSA.
Recent recalls
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Heritage clindamycin oral solution recalled for foreign substanceSold nationwide. Heritage Pharmaceuticals' clindamycin palmitate hydrochloride oral solution (75 mg/5 mL) has been recalled due to the presence of particles and white flakes found in reconstituted bottles. The affected lot is 2411550, which expires November 2026. This product was distributed nationwide.
ModerateFDAAug 19, 2026Heritage Pharmaceuticals
- Clear Eyes Maximum Itchy Eye Relief recalled for potential contamination
Sold nationwide. CLEAR EYES Maximum Itchy Eye Relief eye drops may not be sterile due to potential contamination. The affected product is the 0.5 fl oz (15 mL) dropper bottle, Lot 2552A with expiration date 09/30/2027. No injuries have been reported.
ModerateFDAAug 19, 2026Prestige Brands
- Shoolin Pharma sildenafil and tadalafil powders recalled for manufacturing violations
Sold nationwide. Shoolin Pharma Chem LLP is recalling five bulk powder products, sildenafil citrate and tadalafil in 100-gram, 500-gram, and 1-kilogram sizes, sold for prescription compounding only. The recall was triggered by manufacturing practice (CGMP) deviations found during an FDA inspection, and no injuries have been reported. The products were distributed nationwide.
ModerateFDAAug 19, 2026Shoolin Pharma Chem5 products
- Apollo Care semaglutide vials recalled for particulate matter
Sold nationwide. Apollo Care is recalling 11 strengths of semaglutide sterile multi-dose vials for subcutaneous injection, all sold under the APOLLO care brand. The vials may contain particles identified as nylon/polyamide and silk-like material. The recall covers products distributed nationwide, and no injuries have been reported.
ModerateFDAAug 19, 2026Apollo Care11 products
- Diovan 160 mg tablets recalled for failed dissolution specifications
Sold nationwide. One lot of Novartis Diovan (valsartan) 160 mg tablets failed to meet dissolution specifications, which means the tablets may not dissolve properly in the body. This could affect how well the medication works. The affected lot (AV5913C, expiring 6/2027) was distributed nationwide.
ModerateFDAAug 19, 2026Novartis
Outshine Fruit Bars recalled for possible glassSold nationwide. Dreyer's Grand Ice Cream is recalling select Outshine Fruit Bars because glass may have contaminated the product. The recall affects five flavors (Strawberry, Watermelon, Grape, Tangerine, and Black Cherry) in 6-count and 24-count variety packs. No injuries have been reported so far.
ModerateFDAAug 18, 2026Dreyer's
Gangothri pickled goat and chicken recalled for lack of inspectionSold nationwide. Gangothri Foods (operating as Indus Foods, LLC) recalled approximately 1,626 pounds of ready-to-eat pickled goat and chicken products made between January 2025 and May 2026 because they were produced without USDA inspection. The products were sold to restaurants, retailers, distributors, and consumers nationwide. No illnesses have been reported.
SeriousUSDAAug 17, 2026Gangothri
Hampton Bay Halwin ceiling fans recalled for blade separation riskSold nationwide. The fan blades on some Hampton Bay Halwin 52-inch ceiling fans can separate from the motor flywheel during operation. This poses a risk of impact or injury. The company has received 11 reports of blades breaking or separating, though no injuries have been reported yet.
ModerateCPSCAug 13, 2026Youngo
Sunnyside kerosene fuel containers recalled for flash fire riskSold nationwide. Sunnyside gallon 1-K Kerosene Heater and Appliance Fluid containers lack safety devices required by federal law and pose a risk of flash fire and serious burns. The recalled batch (26082) was sold online and at hardware stores from May through July 2026.
SeriousCPSCAug 13, 2026Sunnyside
Zimtown portable gas cans recalled for burn and poisoning riskSold nationwide. Zimtown 5-gallon portable gas cans sold online have closures that are not child-resistant, violating federal safety standards. Children could open the cans and spill fuel, risking serious burns and poisoning.
SeriousCPSCAug 13, 2026Zimtown
SUGIFT pressure washers recalled for electrocution riskSold nationwide. SUGIFT pressure washers lack a safety device (GFCI) that prevents electrical shock. The short power cord may encourage users to connect an extension cord, which increases the risk of serious injury or death from electrocution.
SeriousCPSCAug 13, 2026Sugift
CuberShop magnetic speed cubes recalled for magnet ingestion riskSold nationwide. CuberShop's Magnetic Stickerless Speed Cubes (model YJ MGC 5×5) come with loose high-powered magnets in the packaging. If swallowed by a child, these magnets can attract each other or metal objects and become trapped in the digestive system, potentially causing serious internal injury or death.
SeriousCPSCAug 13, 2026Sky Cube
Shengsen Prank Sound Makers recalled for battery ingestion riskSold nationwide. These yellow prank sound makers contain coin batteries that children can access and swallow. Swallowing these batteries can cause serious internal burns and death. The products also lack required safety warnings.
SeriousCPSCAug 13, 2026Shengsen Toys
Qabefy twin mattresses recalled for fire riskSold nationwide. Qabefy-branded mattresses sold on Amazon fail to meet mandatory U.S. flammability safety standards, creating a risk of serious injury or death from fire. About 774 mattresses, sold between November 2025 and March 2026, are affected.
SeriousCPSCAug 13, 2026Qabefy
Merax Murphy beds recalled for impact and crush riskSold nationwide. GigaCloud's Merax Murphy beds can fall during assembly or disassembly if not properly installed, posing risk of serious injury. The company has received two reports of beds falling and injuring consumers. The recall affects full-size and twin-size models sold online from May 2024 through February 2026.
SeriousCPSCAug 13, 2026GigaCloud
Yamazuki youth ATVs recalled for brake failure and crash hazardSold nationwide. Yamazuki youth ATVs (model XW-A19, sold under QEASET or HOVERHEART brands) have faulty parking brakes that fail to hold, missing rear safety reflectors, and speed limiters not properly set for children. These defects create a crash hazard and increase the risk of serious injury or death.
SeriousCPSCAug 13, 2026Yongkang Dingchang
COMMOWNER pressure washers recalled for electrocution riskSold nationwide. COMMOWNER 3 GPM electric pressure washers lack proper electrical safety protection and have a short power cord that encourages unsafe extension cord use. This creates a serious risk of electric shock or electrocution.
SeriousCPSCAug 13, 2026AZ Home Concept
Deli fuel containers recalled for child poisoning and burn riskSold nationwide. Deli-branded fuel containers sold on Walmart.com have closures that are not child-resistant, which violates federal safety requirements. Children could open the containers and be exposed to fuel, risking serious burns, poisoning, or other injury.
SeriousCPSCAug 13, 2026Deli OfficeSupplies
DUMOS nine-drawer dressers recalled for tip-over riskSold nationwide. DUMOS Nine-Drawer Fabric Dressers can tip over and trap children if not anchored to the wall. These dressers were sold online as television stand furniture and do not meet federal safety standards for clothing storage units. About 8,981 units were sold.
SeriousCPSCAug 13, 2026Jiayubo
TooyBing wooden bead stacking toys recalled for choking riskSold nationwide. TooyBing wooden bead stacking toys intended for children under 3 years old contain small wooden beads that pose a serious choking hazard. These toys violate federal small parts regulations designed to protect infants and toddlers.
SeriousCPSCAug 13, 2026Guangzhou Yide Toys
Taleco Gear baby jumpers and swings recalled for strangulation riskSold nationwide. Taleco Gear baby jumpers, swings, and 2-in-1 jumper & swing products can become unstable, creating a fall and impact hazard. The hanging restraint straps and seat openings also pose a strangulation risk. The company has received at least 52 reports of these hazards, including 32 reports of injuries such as head bumps.
SeriousCPSCAug 13, 2026Taleco Gear
Brookstone tabletop fire pits recalled for burn injury riskSold nationwide. Brookstone-branded Tabletop Fire Pits can cause uncontrolled fires where flames spread across spilled alcohol and shoot out from fuel containers, causing serious or fatal burns. Southern Telecom has received two reports of flame jetting that resulted in second- and third-degree burns.
SeriousCPSCAug 13, 2026Southern Telecom
Goody King magnetic cubes recalled for magnet ingestion riskSold nationwide. Goody King magnetic building cubes contain magnets that can come loose if the cubes break or open. If a child swallows these loose magnets, they can attract each other inside the digestive system and cause serious injury, including intestinal perforation, blockage, or death.
SeriousCPSCAug 13, 2026Iceberg
Cooluli minifridges recalled for fire and burn hazardsSold nationwide. The electrical switch in certain Cooluli minifridges can short circuit, creating a fire and burn risk. The company has received reports of units smoking, sparking, catching fire, and overheating, with one person injured by smoke inhalation.
SeriousCPSCAug 13, 2026Iceberg
Contego Medical Neuroguard IEP recalled for possible filter failureSold nationwide. The Neuroguard IEP carotid stent and post-dilation balloon system has an integrated filter that may fail to open after the sheath is retracted, due to a wire-to-filter bond issue. If this happens during a procedure, the device may lose its intended embolic protection. No injuries have been reported.
ModerateFDAAug 12, 2026Contego Medical
- Blom-Singer Classic voice prostheses recalled for mislabeling
Sold nationwide. Freudenberg Medical is recalling two Blom-Singer Classic Indwelling Voice Prosthesis products (16Fr/10 mm, REF 1610-LEF and 1610-LF) because the boxes are labeled incorrectly. The box labeled for one product holds the other, so the product inside may not match the label. The recall covers 52 units and was distributed nationwide in the US and to the UK and France. No injuries have been reported.
ModerateFDAAug 12, 2026Freudenberg Medical2 products
- Tissium COAPTIUM Connect recalled for unsubstantiated shelf life
Sold nationwide. The 36-month shelf life on COAPTIUM Connect peripheral nerve repair devices is not substantiated by real-time data, so devices will be relabeled with a 26-month shelf life. Using a device past its validated shelf life may cause it to break during surgery and become unusable; the worst-case outcome would be revision surgery. No injuries have been reported.
ModerateFDAAug 12, 2026Tissium7 products
- GEM Premier 7000, 5000 PAK recalled for solution concentration
Sold nationwide. Instrumentation Laboratory is recalling 141 units of two blood analysis systems: 32 GEM Premier 7000 with iQM3 units and 109 GEM Premier 5000 PAK units. The active ingredient concentration in the lysing bag solution did not meet manufacturing specifications, which could delay recognition and management of co-oximetry and total bilirubin abnormalities. The FDA classified it as Class II, and no injuries have been reported.
ModerateFDAAug 12, 2026Instrumentation Laboratory2 products
- United Orthopedic U2 knee bushing recalled for implant orientation risk
Sold nationwide. United Orthopedic Corp. is recalling three femoral offset bushings (0mm and 4mm, catalog 9323-5310, lot 25FC58) from its U2 Total Knee System. The implant's engraved numbering may be incorrect, which could lead to it being placed in the wrong orientation. The units were distributed in Texas and Michigan, and no injuries have been reported.
ModerateFDAAug 12, 2026United Orthopedic2 products
- Aniara 5-PLASMA Bivalirudin kit recalled for stability issues
Sold nationwide. Aniara Diagnostica LLC is recalling its 5-PLASMA Bivalirudin AMR Verification Kit because stability issues were found with the reconstituted lyophilized human plasma and bivalirudin matrix. These issues cause measurable bivalirudin to degrade in the controls, calibrators, and linearity values. The kit was distributed in IL, NC, and TN, with no injuries reported.
ModerateFDAAug 12, 2026Aniara Diagnostica3 products