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BD Needle Kits used for emergency intraosseous (IO) access may have an obturator (the needle's internal plunger) that locks to the needle hub and becomes difficult or impossible to remove after placement. This locking is caused by out-of-tolerance manufacturing dimensions. If the obturator cannot be removed, a new needle may need to be placed, potentially delaying treatment.

Serious·FDA·Aug 26, 2026

Get Fresh Produce Jalapeno Peppers in 2 lb. and 10 lb. boxes may be contaminated with Salmonella. The affected products were distributed in Illinois, Indiana, Michigan, and Wisconsin. No illnesses have been reported to date.

Serious·FDA·Aug 26, 2026

Dairyland Produce, LLC is recalling jalapeno peppers packaged in 5 lb. clear plastic bags due to potential Salmonella contamination. The affected peppers were distributed in Louisiana and Texas. Consumers who have purchased this product should not use it.

Serious·FDA·Aug 26, 2026

Whole Foods Market is recalling 10 refrigerated guacamole dips, salsas and a trio dip sold in its stores because the jalapeños used to make them may be contaminated with Salmonella. The products were sold in clear plastic containers in AR, IA, IL, IN, KY, LA, MI, MN, MO, OH, OK, TX and WI. No illnesses have been reported.

Serious·FDA·Aug 26, 202610 products

Gifford's HomeMaine ice cream brand Power Play Fudge (one-quart containers) may contain small rubber pieces. The contamination was discovered during production. No injuries have been reported.

Moderate·FDA·Aug 26, 2026·HomeMaine

Grand Central Bakery's Potato Sourdough Bread products may contain metal pieces. Three varieties were affected: Potato Market Loaf (20 oz), Potato Table Loaf (20 oz), and Mini Potato Loaf (12 oz), sold in Washington on August 10, 2026.

Moderate·FDA·Aug 26, 2026·Grand Central Bakery

Lidl US is recalling Vitasia Asian Style Wok Spice Mix after a positive test for Salmonella bacteria. The affected product is the 1.58 oz (45g) package with lot number 155846 and best-if-used-by date of June 2028. This spice mix was sold in Washington DC, Delaware, Georgia, Maryland, North Carolina, New Jersey, New York, Pennsylvania, South Carolina, and Virginia.

Serious·FDA·Aug 26, 2026

Coast Citrus Distributors is recalling bulk jalapeno peppers packaged between July 1–31, 2026, due to potential Salmonella Javiana contamination. The peppers were distributed in bulk containers to wholesale distributors across the central and eastern United States, with further nationwide distribution for food processing. No retail packages or consumer illnesses have been identified.

Serious·FDA·Aug 26, 2026

Publix is recalling four sizes of its store-brand organic frozen berries, including whole blueberries and whole mixed berries in 10 oz and 48 oz bags, because they may be contaminated with E. coli O145:H28. The products were sold in Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee, and Virginia, and no illnesses have been reported.

Serious·FDA·Aug 26, 20264 products

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.

Moderate·FDA·Aug 26, 20264 products

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.

Moderate·FDA·Aug 26, 2026

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.

Moderate·FDA·Aug 26, 202612 products

Some Fresenius Kabi morphine sulfate prefilled syringes are labeled as morphine 2 mg/mL but actually contain Dilaudid (hydromorphone) 0.5 mg/0.5 mL. This labeling error could lead to patients receiving the wrong medication and dose. The affected lot is 6402820 with an expiration date of 12/2028.

Serious·FDA·Aug 26, 2026

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.

Moderate·FDA·Aug 26, 2026

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.

Moderate·FDA·Aug 26, 2026

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.

Moderate·FDA·Aug 26, 2026

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.

Moderate·FDA·Aug 26, 2026·Regeneron

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.

Moderate·FDA·Aug 26, 2026·Shilpa Medicare2 products

Bell Sports is recalling certain Pit Boss motorcycle helmets, size medium, manufactured between January 1 and January 31, 2026. These helmets may lack proper impact protection and do not meet federal safety standards, which increases the risk of head injury in a crash.

Serious·NHTSA·Aug 26, 2026·Bell Sports, Inc.

Shanghai Ravioli Corporation recalled approximately 24,900 pounds of frozen Buffalo chicken ravioli and mozzarella sticks produced without federal inspection. The products, sold to foodservice locations in the Northeast, were marked with a false inspection number and may contain undeclared allergens, harmful bacteria, or other contaminants.

Serious·USDA·Aug 26, 2026·Benedetto's

Jaime's Foods ATX recalled Jaime's Spanish Village Jalapeno Ranch dressing because it contains eggs that were not listed on the label or allergen warning. The omission was discovered during an FDA inspection. People with egg allergies or sensitivities could have a serious or life-threatening allergic reaction if they consume this product.

Serious·FDA·Aug 25, 2026

The Better Bakehouse Snack Company recalled certain lots of Donutful Chocolate Dipped Vanilla Cake Donuts because they may contain milk that is not listed on the label. People with a milk allergy or severe sensitivity could have a serious allergic reaction if they eat this product.

Serious·FDA·Aug 25, 2026

Baxter is recalling two lots of 0.9% Sodium Chloride Injection (saline solution) used in hospitals and dialysis centers because fiberglass particles have been found in the solution. The affected lots were distributed to hospitals and medical suppliers in 14 states between July 31 and August 3, 2026. No injuries have been reported so far.

Serious·FDA·Aug 25, 2026

Baxter is recalling one lot of 70% Dextrose Injection used in hospitals and care facilities because stainless steel particles were found in the solution. If given intravenously, these particles could cause blood clots, block blood vessels, or damage organs. No patient injuries have been reported so far.

Serious·FDA·Aug 25, 2026

Certain 2026 Ford Maverick, F-150, and Bronco Sport vehicles have improperly tightened joints that may come loose. This can cause parts to detach, electrical failures, loss of vehicle control, or fire.

Serious·NHTSA·Aug 25, 2026

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.

Moderate·NHTSA·Aug 25, 2026·Mitsubishi Motors North America, Inc.

Certain 2026 Ford Explorer, Bronco, Bronco Sport, Mustang, and Ranger vehicles have engine pistons that may have been manufactured incorrectly. This defect can cause the pistons to fail, resulting in a sudden loss of engine power while driving, which increases the risk of a crash.

Serious·NHTSA·Aug 25, 2026

Certain 2024–2026 Ford Mustang vehicles have wiring harness ground connections in the engine compartment that may fracture. This can cause loss of engine power, headlights, windshield washers, air conditioning, or cooling fan function. Loss of power or headlights increases crash risk.

Serious·NHTSA·Aug 25, 2026

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.

Moderate·NHTSA·Aug 24, 2026

Rennline's lower control arm (part number S180) may have been made with incorrect dimensions, which can damage the vehicle's subframe. A damaged subframe can cause loss of steering control and increase crash risk.

Serious·NHTSA·Aug 24, 2026·Rennline Automotive