Maine recalls

Utz Quality Foods is recalling 1.5 oz and 8 oz bags of Zapp's Big Cheezy Potato Chips because they may contain Salmonella, a bacteria that can cause serious illness. The affected bags were distributed across 33 states. No illnesses have been reported so far.

Utz Quality Foods is recalling 2.0 oz bags of Dirty Maui Onion Chips because they may contain Salmonella, a bacteria that can cause serious illness. The affected products were distributed across 33 states.

Utz Quality Foods is recalling 1.5oz and 2oz bags of Dirty Brand Salt and Vinegar Potato Chips because they may contain Salmonella. The affected products were distributed across 33 states. No illnesses have been reported to date.

Utz Quality Foods is recalling Zapp's Brand Bayou Blackened Ranch Potato Chips in 2.5 oz and 8 oz bags because they may contain Salmonella. The affected products were distributed across 32 states. No illnesses have been reported.

Utz Quality Foods is recalling 1.5oz bags of Zapp's Bayou Blackened Ranch Kettle Chips because they may contain Salmonella, a bacteria that can cause serious illness. The affected bags were distributed across 33 states.

Spring & Mulberry Blood Orange Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is sold individually and in multi-packs on Amazon, as well as in wholesale cases. Three specific lot codes and use-by dates are involved.

Spring & Mulberry Coffee Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is sold individually and in multi-packs on Amazon, as well as through wholesale distribution. The recall includes specific lot numbers with use-by dates ranging from February to June 2027.

Spring & Mulberry Sea Salt Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is a 2.1 oz bar sold individually or in multi-packs, with specific batch/lot numbers 026013 and 026014, use-by date 07/31/2027, and UPC 850055470071.

Spring & Mulberry Pure Dark and Pure Dark Minis chocolate bars may be contaminated with Salmonella. The affected products were distributed nationwide in individual bars and multi-packs. No illnesses have been reported.

Spring & Mulberry Pecan Date Date-Sweetened Chocolate bars may be contaminated with Salmonella. The recall affects specific batches with expiration dates ranging from August 2026 through December 2026. The bars are sold individually and in multi-packs on Amazon.

Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is sold individually and in multi-packs (3, 6, or 12-packs) on Amazon, as well as wholesale.

Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars may be contaminated with Salmonella. The recall affects approximately 17,848 individual bars sold nationwide, including bars sold on Amazon in single and multi-packs.

Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars may be contaminated with Salmonella. The recall affects specific batch lots with use-by dates ranging from January through August 2027. No illnesses have been reported.

Spring & Mulberry Earl Grey Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is a 2.1 oz. chocolate bar in a purple box sold individually and in multi-packs on Amazon, with specific lot numbers and use-by dates identified.

Spring & Mulberry Mixed Berry Date-Sweetened Chocolate bars (2.1 oz) may be contaminated with Salmonella. The affected product was distributed nationwide and sold individually and in multi-packs on Amazon. Salmonella can cause serious illness.

Potential Salmonella contamination

Motor City Pizza Co. 5 Cheese Bread products may contain Salmonella, a bacteria that can cause serious illness. The affected products were distributed nationwide to major retailers including Costco, Walmart, Target, and Kroger.

Sun Pharmaceutical discovered that some bottles labeled as containing 6mg Perampanel tablets actually contained 10mg tablets instead. This mix-up affects one lot (AE01763) distributed nationwide. Patients taking the wrong strength could receive an incorrect dose of this seizure medication.

Elevate Oral Care's Povi-One 10% Povidone-Iodine Oral Antiseptic does not contain the full strength stated on the label. Five specific production lots distributed nationwide do not meet the required potency standard, which means the product may not work as intended for oral antiseptic purposes.

Some bottles of Lacosamide 100mg tablets may contain Selexipag 1000 mcg tablets instead. This mix-up happened during manufacturing and could cause patients to take the wrong medication. The recall affects specific lots distributed nationwide.

BD ChloraPrep FREPP Clear, a sterile skin antiseptic applicator, may contain fungal contamination (Aspergillus penicillioides) or may not be fully sterile due to wrinkles in the packaging seal. Approximately 178,000 applicators from lot 4073005 (expiring 03/31/2027) are affected nationwide and internationally.

BD ChloraPrep Clear, a sterile antiseptic skin-prep solution used before medical procedures, was found to contain Aspergillus penicillioides fungus in some applicators. This affects the sterility of the product, which is critical for medical use. The affected lot is Lot #4032183 with an expiration date of January 31, 2027.

BD ChloraPrep FREPP Clear applicators may have wrinkles in the paper lid that could compromise the sterile seal. This affects multiple lot numbers distributed nationwide through mid-2027. No injuries have been reported.

BD ChloraPrep Clear, a sterile skin antiseptic solution used before medical procedures, is being recalled because wrinkles in the paper packaging lid may allow the sterile seal to be breached. This defect could potentially allow contamination of the product. No injuries have been reported.

ANI Pharmaceuticals is recalling hydroxyzine hydrochloride oral solution (10 mg/5 mL, 473 mL bottles) due to the presence of a foreign substance in one lot. The affected product was distributed nationwide. No injuries have been reported.

Direct Rx's packaged Duloxetine D/R 30 mg capsules contain levels of N-nitroso-duloxetine, a potentially harmful impurity, above FDA's recommended limit. This is a manufacturing quality issue affecting specific lots distributed nationwide.

Amgen is recalling Sensipar (cinacalcet) 90mg tablets due to deviations from current good manufacturing practice (CGMP) standards. This affects one lot distributed nationwide. No injuries have been reported.

Amgen is recalling specific lots of Corlanor (ivabradine) 7.5mg tablets due to the presence of a foreign substance in some bottles. The affected lots were distributed nationwide. No injuries have been reported.

Amgen is recalling Sensipar (cinacalcet) 60mg tablets due to deviations from manufacturing standards. The recall affects one lot (1157055) with an expiration date of January 31, 2028, distributed nationwide.

Amgen is recalling Sensipar (cinacalcet) 30mg tablets due to deviations from manufacturing quality standards (CGMP). The recall affects one specific lot distributed nationwide. No injuries have been reported.