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Search every CPSC, FDA, USDA and NHTSA recall on record, or scan a barcode. The last 90 days are below.
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Page 16 of 45Moderate
- Prospector Popcorn gourmet popcorn recalled for nutrition labeling errors
Prospector Popcorn is recalling four gourmet popcorn flavors: Chocolate Mocha, Maple Walnut Ice Cream, Fudge Brownie, and Belgian Chocolate Toffee, in 1.5 oz and 3.5 oz sizes. The nutrition labels understate carbohydrate and cholesterol amounts. No illnesses or injuries have been reported.
ModerateFDAAug 26, 20264 products
- Nutrient Foods Cocoa Crunch recalled for undeclared soy
Nutrient Foods' Protein Cereal Cocoa Crunch contains soy but does not declare it on the label. People with soy allergies or sensitivities could have a serious reaction if they consume this product. The affected product was distributed to 10 states.
ModerateFDAAug 26, 2026
- American Regent injectables recalled for glass and hair contamination
American Regent is recalling 12 injectable and oral solution products, including nitroglycerin, cyanocobalamin (vitamin B12), aminocaproic acid, atropine, acetylcysteine, selenious acid, papaverine, niCARdipine, and the trace element products Multrys and Tralement. Some vials may contain particulate matter identified as hair, glass, and/or paraformaldehyde. No injuries have been reported.
ModerateFDAAug 26, 202612 products
- Mylan Acamprosate Calcium recalled for dissolution failure
Mylan Pharmaceuticals is recalling one lot of Acamprosate Calcium 333 mg delayed-release tablets because they failed to meet dissolution specifications—meaning the tablets may not break down and release the medication as intended in the body. This could result in ineffective treatment. No injuries have been reported.
ModerateFDAAug 26, 2026
- Golden State Medical Supply Carbamazepine tablets recalled for black specks
Golden State Medical Supply is recalling Carbamazepine Tablets, USP 200mg due to black specks found in some tablets. This is a manufacturing quality issue. The affected lots were distributed nationwide.
ModerateFDAAug 26, 2026
- Sun Pharmaceutical Carbamazepine recalled for tablet defect
Sun Pharmaceutical's Carbamazepine 200mg tablets (Lot #AD94033, expiring 5/31/2028) contain black spots caused by burnt ingredients during manufacturing. The tablets do not meet quality standards, though no injuries have been reported.
ModerateFDAAug 26, 2026
- Regeneron Libtayo injection recalled for sterility concerns
Regeneron is recalling one lot of Libtayo (cemiplimab-rwlc), an intravenous cancer treatment, because the manufacturer cannot guarantee the vials are sterile. This affects lot 8494000002, which expires July 31, 2028. About 21,353 vials are involved in the recall nationwide.
ModerateFDAAug 26, 2026Regeneron
- PEMRYDI RTU pemetrexed injection recalled for discoloration
Certain vials of PEMRYDI RTU (pemetrexed injection) have developed green to dark green discoloration. The affected lots are P400172 and PA00050A, expiring 09/30/2027. Discoloration may indicate a quality issue with the medication.
ModerateFDAAug 26, 2026Shilpa Medicare2 products
- Mitsubishi Outlander recalled for rearview camera display failure
Certain 2025–2026 Mitsubishi Outlander and 2026 Outlander PHEV vehicles have a software error that prevents the rearview camera image from displaying when the vehicle is in reverse. Without the camera view, drivers have reduced visibility behind the vehicle, which increases crash risk.
ModerateNHTSAAug 25, 2026Mitsubishi Motors North America, Inc.
- Thomas Built SAF-T-LINER school buses recalled for structural defects
Certain 2027 Thomas Built SAF-T-LINER HDX2 and EFX2school buses may have missing connector plates on the driver's seat belt anchor and interior body joints. These missing parts reduce structural strength and could prevent the seat belt from properly restraining the driver in a crash.
ModerateNHTSAAug 24, 2026
Vitruvias Thyroid Tablets recalled for super potency riskVitruvias Therapeutics is recalling one lot (504950) of Thyroid Tablets, USP 30 mg because testing found the tablets may contain higher-than-intended amounts of thyroid hormone. Taking overly potent thyroid medication can cause an overactive thyroid, leading to weight loss, rapid heartbeat, chest pain, and other serious symptoms, especially in elderly people, pregnant women, and infants.
ModerateFDAAug 21, 2026Vitruvias Therapeutics
- Cornell Pump trailers recalled for cracked tongue instability
Cornell Pump Company is recalling certain 2025 Enclosed Pump Trailers and Utility Pump Trailers because the trailer tongue may crack over time. A cracked tongue can cause the trailer to become unstable while towing, increasing the risk of a crash.
ModerateNHTSAAug 21, 2026Cornell Pump Company LLC
- Altec Industries vehicles recalled for delayed braking risk
Altec Industries is recalling certain 2019–2026 AN Series, 2023 AA Series, 2022–2026 Digger Derrick, and 2025 AM Series vehicles. The Bendix automatic braking system was not recalibrated after the front radar box was relocated, which can cause a delayed braking response and increase crash risk.
ModerateNHTSAAug 21, 2026
- Marathon Industries F-650 liftgate recalled for deck pin failure risk
The liftgate deck pins on certain 2025 Ford F-650 SD vehicles may break, causing the liftgate platform to fall unexpectedly. This can result in injury to people nearby.
ModerateNHTSAAug 20, 2026Marathon Industries Inc.
- GM Buick and Chevrolet vehicles recalled for faulty rearview camera
The rearview camera screen in certain 2024–2025 Buick Envista and Encore GX, Chevrolet Trailblazer, and 2025 Chevrolet Trax vehicles may display a distorted or blank image. A camera that does not work properly reduces your ability to see behind the vehicle, increasing crash risk.
ModerateNHTSAAug 20, 2026
- Britax child seats recalled for carrying handle detachment risk
A screw in the carrying handle of certain Britax child seats (B-Safe Gen 2, B-Safe Gen 2 Flexfit, B-Safe Gen 2 Flexfit Plus, B-Safe 35, B-Safe Ultra, and Endeavours models) may loosen and cause the handle to partially detach. If the handle detaches while a child is being carried, the child could fall.
ModerateNHTSAAug 20, 2026Britax Child Safety, Inc.
- Honeyville Yellow Color recalled for undeclared Red #40
Honeyville Yellow Color 1 Gallon contains undeclared Red #40 food dye, which is not listed on the label. The product was distributed to food manufacturers in Nevada, Arizona, Oregon, and California. People with allergies or sensitivities to Red #40 could have an adverse reaction if exposed without knowing the ingredient is present.
ModerateFDAAug 19, 2026
- SHEANDRO Vodka Tomato Sauce recalled for undeclared milk
SHEANDRO LLC's Vodka Tomato Sauce contains milk from cream and cheese ingredients, but the label does not declare milk as an allergen. People with milk allergies or sensitivities who consume this product could have a serious allergic reaction.
ModerateFDAAug 19, 2026
- Heritage clindamycin oral solution recalled for foreign particles
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 sterility risk
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
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
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
- Novartis Diovan 160 mg recalled for dissolution failure
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
- Lyle Style Bloody Mary Mix recalled for undeclared soy
Lyle Style Mild Bloody Mary Mix (32 oz glass bottles, UPC 7 84762 03730 3) contains soy in the Worcestershire sauce ingredient, but the label does not disclose this allergen. The product was distributed in Oregon and Washington with production dates from July 28, 2025 to July 28, 2026.
ModerateFDAAug 19, 2026
- E-One fire trucks recalled for outrigger hydraulic valve failure
Certain 2025–2026 E-One Cyclone and Typhoon fire trucks may have a hydraulic valve that fails, preventing the outriggers from extending or retracting. Outriggers stabilize the truck during emergency operations; if they cannot move, response time and crew safety may be compromised.
ModerateNHTSAAug 19, 2026E-One Incorporated
- Avride ADS software recalled for unexpected vehicle movement
Avride's automated driving system software (versions before RC-01-05) may direct vehicles to change lanes, merge, or veer without safely checking for other vehicles or maintaining distance. This unexpected movement increases crash risk.
ModerateNHTSAAug 19, 2026Avride Inc.
Outshine Fruit Bars recalled for possible glassDreyer'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
- Heil Co. garbage trucks recalled for CNG fuel leak risk
Certain 2016–2026 Heil front loader garbage trucks with replacement CNG tailgate ladder kits may have an incorrect bolt installed in one ladder leg. This bolt can contact and damage the CNG cylinders, which may leak fuel and increase fire risk.
ModerateNHTSAAug 17, 2026The Heil Co.
- Ring Power digger derrick trucks recalled for pole guide arm fall risk
Certain 2019–2026 Terex and General digger derrick trucks sold by Ring Power have a weld defect that may crack and cause the retaining pin to separate. If that happens, the pole guide arm can fall, potentially injuring workers or bystanders nearby.
ModerateNHTSAAug 17, 2026Ring Power Corporation
- Chrysler, Jeep, Dodge, Ram recalled for rearview camera failure
The rearview camera image may fail to display when certain 2026–2027 Chrysler, Jeep, Dodge, and Ram vehicles are placed in reverse. This reduces the driver's ability to see behind the vehicle, increasing crash risk. A software update will fix the problem.
ModerateNHTSAAug 13, 2026