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ICU Medical is recalling three Plum infusion pump models, covering 13,613 units each. Under certain conditions, the pump may not show a soft limit alert or warn the clinician of a soft limit violation before delivery starts, which could lead to under- or over-delivery of medication. No injuries have been reported.

Moderate·FDA·Jun 17, 20263 products

A manufacturing defect in the Fresh Roast Systems ColorTrack model BENCH R-100 could, under rare misuse conditions, expose users to infrared laser light levels higher than the product's safety rating. No injuries have been reported. The defect affects a small number of units.

Moderate·FDA·Jun 17, 2026·Fresh Roast Systems

Wild Coast Brew is recalling three loose-leaf tea products: The Shadow Winter Spice Black Tea, The Creator Ginger Lemongrass Tisane, and The Lover Tart Chocolaty Tisane. The teas contain ashwagandha root, which the FDA considers an unsafe food additive. The products were sold nationwide, and no injuries have been reported.

Moderate·FDA·Jun 17, 2026·The Shadow3 products

Sensory Supplement LLC is recalling Neuro Nourish, a 6-in-1 dietary supplement, due to premature lipid oxidation during storage. Affected product may have an off odor and bitter taste, though no injuries have been reported.

Moderate·FDA·Jun 17, 2026·Neuro Nourish2 products

U.S. Trading Company is recalling DRAGONFLY Thai Ginger Powder (4.37 oz) because it may contain lead. The powder was distributed across multiple U.S. states. No injuries have been reported.

Moderate·FDA·Jun 17, 2026

Park St. Deli Macaroni & Cheese (20 oz packages) contains soy lecithin that is not listed on the label. People with a soy allergy or sensitivity could have a serious reaction if they eat this product without knowing soy is present.

Moderate·FDA·Jun 17, 2026

Mothers' Milk Bank of Louisiana is recalling specific batches of pasteurized donor human milk (3 oz bottles) because a dark spot was found on the bottom of some containers, which could indicate physical contamination. The affected batches are limited to 32 bottles with expiration date 08/24/2026.

Moderate·FDA·Jun 17, 2026·MMB of Louisiana

Galaxy is recalling 23 refrigerated Latin-style cakes, rolls, cheesecakes and related bakery items sold in plastic clamshell containers, including Brazo Gitano, Napolitano, Rollitos, Cake de Capuchino, Marquesita, Cheesecake and Flan Cake products. The products may contain Yellow #5, Yellow #6 or Red #40 without listing them on the label. The products were distributed in Florida and Texas, and no injuries have been reported.

Moderate·FDA·Jun 17, 202623 products

Refresqueria Estrella Inc. is recalling Bebida de Parcha (passion fruit drink) in multiple sizes because the product contains FD&C Red 40 food coloring that was not declared on the label. This affects bottles sold in Puerto Rico with specific production lot codes and expiration dates from March through May.

Moderate·FDA·Jun 17, 2026

Rich Products Corp is recalling Farm Rich Pizza Cheese Crunchers because they may contain metal pieces. The affected products have lot number 003029976 with a best-by date of 7/30/27. No injuries have been reported.

Moderate·FDA·Jun 17, 2026·Farm Rich

Sun Pharmaceutical has recalled budesonide inhalation suspension (1mg/2mL single-dose ampules) due to the presence of black or brown specs and particles found in some vials. The affected lot is BAG0074A with an expiration date of January 31, 2027. This is a quality issue that could affect the safety and sterility of the medication.

Moderate·FDA·Jun 17, 2026

Ascend Laboratories is recalling Minocycline Hydrochloride Extended-Release Tablets, 115 mg (lot 25141635, expires 4/30/2028) because testing found the tablets did not dissolve properly as required. This affects 360 bottles distributed nationwide. No injuries have been reported.

Moderate·FDA·Jun 17, 2026

Golden State Medical Supply is recalling specific lots of niacin extended-release tablets (1,000 mg) because they failed to dissolve properly during stability testing. The tablets did not meet dissolution specifications at the 24-hour mark, which means they may not release the medication as intended in the body.

Moderate·FDA·Jun 17, 2026

Zep Inc. is recalling Alcohol Sanitizer Spray (Ethanol 70%, 55-gallon drums) due to microbial contamination. The affected batch (E2612116, expiration April 2029) was distributed nationwide. A total of 5 drums are involved.

Moderate·FDA·Jun 17, 2026·Zep

Amneal Pharmaceuticals is recalling Primidone 50 mg tablets (NDC 53746-544-01, lot AM251676) due to potential cross-contamination with Acemetacin during manufacturing at the API supplier. The contamination could affect the safety or effectiveness of the medication.

Moderate·FDA·Jun 17, 2026

Breckenridge is recalling two sizes of duloxetine delayed-release capsules, 30 mg and 60 mg, made by Towa Pharmaceutical Europe in Spain. The recall covers about 374,400 bottles distributed nationwide. The capsules contain an impurity called N-nitroso-duloxetine at a level above the FDA's recommended interim limit. No injuries have been reported.

Moderate·FDA·Jun 17, 20262 products

Fresenius Kabi USA is recalling specific batches of epinephrine injection due to failed impurity and degradation specifications. The affected vials may not meet required purity standards. No injuries have been reported.

Moderate·FDA·Jun 17, 2026

Beekeeper's Naturals Saline Nasal Spray was manufactured without proper sterilization, allowing microbial contamination. The affected product is Lot #5950 with an expiration date of 02/2028. No injuries have been reported so far.

Moderate·FDA·Jun 17, 2026·Beekeeper's Naturals

Waymo's 5th Generation Automated Driving System software could allow vehicles to enter and drive through closed freeway construction zones at full speed. This increases the risk of a crash. Waymo has released a free software update to detect and avoid construction zones.

Moderate·NHTSA·Jun 13, 2026

Deck pins on certain Waltco MDV series liftgates installed on Morgan aluminum dry vans may break, causing the liftgate platform to fall unexpectedly. This poses a risk of injury to people nearby.

Moderate·NHTSA·Jun 12, 2026·Marion Body Works Inc.

Azuma Foods recalled 545 cases of Tako Wasabi seasoned octopus because they may contain undeclared fish. A supplier changed an ingredient from mollusk extract to bonito (a type of fish) without notifying the manufacturer. People with fish allergies could have a serious allergic reaction.

Moderate·FDA·Jun 11, 2026·Azuma Foods

Yamaha UMAX Bistro and Bistro Deluxe vehicles (Model Years 2019–2025) have an incorrect weight capacity label. If the label is wrong, the vehicle could be overloaded, creating a risk of injury to operators or bystanders.

Moderate·CPSC·Jun 11, 2026

The drive converter sheave in certain 2026 Kawasaki Teryx4 H2 and Teryx5 H2 off-road vehicles can break during operation, releasing metal fragments into the engine compartment. Kawasaki has received 19 reports of this issue, though no injuries have been reported yet.

Moderate·CPSC·Jun 11, 2026·Kawasaki

Albertsons store-made 8-inch carrot cakes were sold without proper allergen labeling. The cakes contain pecan or walnut but the labels do not declare these nuts, posing a risk to people with nut allergies. About 167 cakes with a "Packed On" date of May 5 or earlier are affected.

Moderate·FDA·Jun 10, 2026121 products

UC Health Milk Bank's pasteurized donor human milk may contain small plastic particles. The contamination was identified in specific lot codes of both standard (100 mL) and pediatric (200 mL) bottles distributed to medical facilities and consumers in California.

Moderate·FDA·Jun 10, 2026·University of California Health Milk Bank

Lunds & Byerly's Curry Powder Sweet bottles were filled with sesame seeds but labeled as curry powder. This mislabeling creates a risk for people with sesame allergies who may consume the product expecting curry powder. The affected lot code is 0082026U00232 with a best-by date of 01/26/2029.

Moderate·FDA·Jun 10, 2026

Second Nature Keto Crunch Smart Mix 10-ounce pouches may contain undeclared cashews, pistachios, and dried cherries. These allergens are not listed on the label, which is a serious concern for people with tree nut allergies. The product was distributed nationwide through retail stores and online.

Moderate·FDA·Jun 10, 2026

Market of Choice Vegan Kale Caesar Salad contains sesame seeds in the Za'atar spice mixture, but sesame is not listed on the label. People with sesame allergies could have a serious reaction if they eat this product.

Moderate·FDA·Jun 10, 2026

Jesse's Bakery is recalling two coleslaw products, My Wife's Slaw and My Wife's Slaw Jalapeno Heat, sold in 8 oz. and 16 oz. glass mason jars. The products were made and distributed without an approved food establishment inspection, and the required safety parameters could not be verified. They were sold in Alabama, Ohio, Texas, and West Virginia, and no injuries have been reported.

Moderate·FDA·Jun 10, 2026·My Wife's Slaw2 products

Creative Compounds, LLC is recalling Betaine Anhydrous (Lot SWT2025100101, expiration September 2027) because it may contain small pieces of carbon steel (1–2mm). The affected material was distributed to five accounts in Florida, New Jersey, Texas, Georgia, and Oregon.

Moderate·FDA·Jun 10, 2026·Creative Compounds