Oregon recalls

Philips Respironics has recalled certain Trilogy EV300 home ventilators (software version 1.05.15.00) because the obstruction alarm may not trigger quickly enough if the breathing tube becomes blocked. In rare cases, the alarm could be delayed by up to four breaths, which is longer than safety standards allow.

Some Philips Respironics Trilogy Evo O2 ventilators with software version 1.05.15.00 may not sound an obstruction alarm quickly enough if the breathing tube becomes blocked. The alarm could be delayed by up to four breaths, which could reduce the time available to respond to a blockage.

Some Philips Respironics Trilogy Evo home ventilators with Software Version 1.05.15.00 may not sound their obstruction alarm quickly enough if the breathing tube becomes blocked. The alarm could be delayed by up to four breaths, which could reduce the time a user has to respond to an airway obstruction.

Abiomed's Impella Controller may display a delayed "Purge System Blocked" alarm when used with first-generation Impella 5.5 pumps. This could prevent timely detection of a blocked purge system. The issue affects 62 controllers with specific serial numbers in software versions 8.2.2 through 8.5.

Abiomed is recalling purge cassettes used in Impella heart pump systems because Generation 1 cassettes have an increased risk of leaking during use. This affects multiple Impella pump models sold globally, with specific batch numbers identified from 2024.

Imu-Tek Colostrum-5 Powder (Lot #22, expiration 020528) may not have been processed adequately, which could allow harmful bacteria to survive. The affected product was distributed across 29 states. No illnesses have been reported so far.

Imu-Tek Animal Health is recalling Colostrum-5 120-capsule bottles (Lot #013, expiration 092826) because the product may be under-processed, which can affect its safety. The affected bottles were distributed across 33 states.

Mei Heong Yuen Garlic Flavor Roasted Peanuts (9.17 oz) contain cyclamates, a sweetener banned in the United States. The product was distributed to multiple states under UPC 6912449124329 with manufacture date July 10, 2025. No injuries have been reported.

Mei Heong Yuen walnut-flavor roasted peanuts contain sodium cyclamate, a sweetener banned in the United States. The 9.17 oz packages were distributed to multiple states. No illnesses have been reported.

Mei Heong Yuen tangerine flavor roasted peanuts contain sodium cyclamate, a sweetener banned in the United States. The product was distributed to 19 states. No injuries have been reported.

Lone Star Dairy Products LLC is recalling spray dried milk powder products because Salmonella bacteria was found during testing of finished products. The recall affects specific lot codes of NFDM Low Heat, NFDM High Heat, and SMP Medium Heat products sold in 25 kg bags and 1 metric ton totes.

Divided Sunset Multi Collagen Peptides (8 oz pouch) contain egg and fish ingredients but do not clearly label them as allergens on the package. The ingredient list mentions eggshell membrane collagen and marine collagen but fails to state "EGG" or identify the fish species as required by law. This poses a risk to people with egg or fish allergies.

Some cartons of Amneal Magnesium Sulfate IV bags were mislabeled and contained Tranexamic Acid (a different medication) instead. This mix-up affects lot AH250162 with an expiration date of 8/31/2027. The error was discovered before the product reached patients.

Appco Pharma LLC is recalling specific lots of prazosin hydrochloride 5mg capsules because they contain higher-than-acceptable levels of a nitrosamine impurity (N-nitroso-prazosin). Nitrosamines are chemical contaminants that may increase health risks with long-term exposure. This is a manufacturing quality issue, not a safety defect in the drug itself.

Appco Pharma LLC is recalling specific lots of prazosin hydrochloride 2mg capsules because they contain higher-than-allowed levels of a nitrosamine impurity called N-nitroso-prazosin. Nitrosamines are chemicals that may increase cancer risk with long-term exposure. No injuries have been reported so far.

Appco Pharma LLC is recalling prazosin hydrochloride 1mg capsules (100-count bottles) because they may contain higher-than-acceptable levels of a nitrosamine impurity. This impurity was detected during manufacturing quality checks. The recall affects specific lot numbers distributed nationwide.

Multiple brands of artificial tears eye drops made by K.C. Pharmaceuticals have been recalled because the manufacturer cannot confirm the product is sterile. The affected drops are sold under store brands including Leader, Good Sense, Good Neighbor Pharmacy, TopCare, Best Choice, Kroger, Publix, and Quality Choice. No injuries have been reported.

K.C. Pharmaceuticals issued a recall of Rugby Lubricating Eye Drops and Walgreens Lubricant Eye Drops because the manufacturer cannot guarantee the products are sterile. Non-sterile eye drops can introduce bacteria or other microorganisms into the eye. The recall affects specific lots (SY24K01 and SY24K02) with expiration dates of 09/30/26.

K.C. Pharmaceuticals has recalled multiple brands of sterile redness relief eye drops because they may not meet sterility standards. The affected products were distributed nationwide under various store and pharmacy brand names. No injuries have been reported so far.

K.C. Pharmaceuticals issued a recall of sterile eye drops sold under multiple brand names (including Walgreens, Good Sense, Kroger, CVS, and others) because the manufacturer cannot confirm the products remain sterile. The affected bottles were distributed nationwide. No injuries have been reported.

K.C. Pharmaceuticals is recalling multiple brands of ultra lubricating eye drops sold nationwide because the manufacturer cannot guarantee the drops are sterile. The affected products were distributed under names including Leader, Harris Teeter, Foster & Thrive, Walgreens, CVS Health, Kroger, Publix, Meijer, Good Sense, Quality Choice, and Avenova. No injuries have been reported.

K.C. Pharmaceuticals is recalling Dry Eye Relief Eye Drops sold under multiple store brands including Geri Care, TopCare, Rite Aid, Leader, and others due to concerns that the product may not be sterile. The recall affects 15 mL bottles with specific lot numbers and expiration dates sold nationwide.

K.C. Pharmaceuticals' Advanced Relief eye drops in 0.5 fl oz bottles may not be sterile due to a manufacturing issue. The affected products were sold under multiple store brands at Walgreens, Kroger, CVS, and other retailers nationwide. No infections have been reported so far.

K.C. Pharmaceuticals has recalled multiple brands of sterile eye drops (including Best Choice, Quality Choice, Discount Drug Mart, Good Sense, Walgreens, CareOne, Equaline, TopCare, Meijer, and H.E.B.) because the manufacturer cannot guarantee the products are sterile. Non-sterile eye drops can introduce infection into the eye. The affected products were distributed nationwide and have lot number AC24E01 with expiration date 05/31/26.

Amneal Pharmaceuticals is recalling specific lots of tramadol 50 mg tablets because they contain higher-than-allowed levels of a chemical impurity called N-nitroso-desmethyl-tramadol (NDSRI). The impurity was discovered during stability testing of tablets nearing the end of their shelf life. No injuries have been reported.

Alembic Pharmaceuticals is recalling specific lots of Bromfenac Ophthalmic Solution 0.07% because the medication failed purity and degradation tests during stability testing at 20 months. The affected eye drops may contain higher-than-acceptable impurity levels, which could affect safety and effectiveness.

Nalpac is recalling DTF Sexual Chocolate because it contains sildenafil and tadalafil—prescription drug ingredients found in Viagra and Cialis—that were not listed on the label. These hidden ingredients can dangerously lower blood pressure, especially if you take nitrate medications like nitroglycerin.

Liquid Blenz Corp. is recalling all Good Brain Tonic beverages (16 oz and 32 oz bottles) due to a potential botulism risk. Botulism is a serious form of food poisoning. No illnesses have been reported yet, but the product was distributed nationwide.

The USDA retracted a public health alert issued on April 1, 2026, for Walmart Great Value Fully Cooked Dino Shaped Chicken Breast Nuggets with a "Best If Used By" date of February 10, 2027. The initial alert was based on a laboratory test that showed elevated trace levels of lead, but follow-up testing found no lead contamination in the product. The USDA determined the original test result was a false positive caused by contamination in the laboratory during analysis, not in the food itself.

Raw Farm has recalled specific batches of raw cheddar cheese products (blocks and shredded) due to a potential link to an E. coli O157:H7 outbreak. The recall includes multiple batch numbers and expiration dates listed on the Raw Farm website. No pathogens have been found in Raw Farm products tested so far.