1,215 recalls tagged with “replacement available”.
Wagner Spray Tech recalls 900 Series power steamers, including the 905e Auto Steamer, 915e On-Demand Power Steamer, and 925e Steam Machine Elite Steamer. The recall cites a burn hazard from an overheating hose and hot-water expulsion from the nozzle. Consumers should stop using the recalled steamers immediately and contact Wagner for a free repair kit.
Electrolux Group recalled Frigidaire gas ranges sold nationwide through retailers after a burn hazard was identified. The bake burner can ignite with delay, creating a burn risk. Stop using the recalled ovens immediately and contact Electrolux for a free in-home bake burner repair; cooktops remain usable.
Specialized recalled all Turbo Como SL electric bicycles sold online at specialized.com and through Authorized Specialized Retailers. A fatigue crack in the fork steerer tube can cause progressive fork failure and a fall. Owners should stop riding immediately and arrange a free fork replacement at an Authorized Dealer; replacement parts are expected in Spring 2026.
Amazon recalled the Amazon Basics Camping Folding Pocket Knife sold by Amazon after a laceration hazard was identified. The knife has a 3.5-inch blade. The folding mechanism can fail to remain securely closed, posing a risk of serious cuts.
Lifetime Brands recalls BUILT LUUM Light Up Tumblers sold at multiple retailers. The recall covers 16 oz and 18 oz plastic cups with a lid and straw that contain a bottom LED light powered by a button cell battery. Labels on the underside or hangtags show the theme and item numbers with UPCs. Stop using these tumblers immediately and seek a full refund by contacting Lifetime Brands.
Straumann USA recalled 13 Custom Abutment Ti RC units distributed worldwide, including the United States and Canada. A TAN material was misidentified as Titanium Ti Gr4 D during manufacturing, causing RC Titanium abutments to be made from TAN material. Clinics and patients should stop using the devices immediately and follow recall instructions from Straumann USA or their healthcare providers.
Straumann USA LLC recalls 7 Custom Abutment AS Ti for Straumann RC. The recall follows a material mix-up during manufacturing. A TAN material bar was incorrectly identified as Titanium Bar Ti Gr4 D, causing RC Titanium abutments to be made with TAN material. Stop using the device and contact Straumann for instructions immediately.
Teva Pharmaceuticals recalled 1,897 cartons of Octreotide Acetate for Injectable Suspension distributed nationwide in the USA after an FDA inspection flagged sterility concerns. The recall is due to lack of assurance of sterility from the contract manufacturer. Consumers and healthcare providers should stop using the product immediately and contact Teva for guidance.
Xanax XR extended-release alprazolam recall issued March 17, 2026 remains active. Viatris Specialty LLC distributes the drug nationwide in the United States. The issue is failed dissolution specifications. Patients and healthcare providers should stop using the product immediately and follow the recall instructions for guidance.
POCAS INTERNATIONAL recalled 425 cases of POPPING BOBA RTD Strawberry Dragon F/OOLONG Tea distributed in NY, VA, FL, MA, TX, LA, UT, CA and Canada. The recall cites a packaging integrity issue that may compromise product quality. Consumers should not consume the product and should contact Pocas International by email for refunds or replacements.
Lucerne recalled 12,222 tubs of 2% cottage cheese sold at Albertsons stores after metal fragments were found in packaging. The object is a curled stainless steel spring and could end up in the product. Stop using the product and contact Albertsons Companies LLC for a refund or replacement.
Meclizine Hydrochloride Tablets distributed nationwide by Amerisource Health Services LLC are being recalled. The two affected NDCs are 60687-775-65 and 60687-775-11. The recall is due to failed tablet specifications. Stop using the product and contact a healthcare provider for guidance immediately.
Pocas International recalled 517 cases of Popping Boba RTD Mango Passion Fruit Green Tea distributed to NY, VA, FL, MA, TX, LA, UT, CA and Canada. A packaging integrity issue may compromise product quality. Consumers who purchased it should not consume the beverage and should contact Pocas International for refund or replacement via email.
Pocas International Corp. recalls 148 cases of POPPING BOBA RTD Mixed Berry Hibiscus Tea distributed to New York, Virginia, Florida, Massachusetts, Texas, Louisiana, Utah, California and Canada. A packaging integrity issue may compromise product quality. Consumers who purchased should not consume it and should contact Pocas International for refund or replacement information via email.
Cipla USA Inc. recalls 54,583 Lanreotide acetate injections nationwide after FDA flagged sterility assurance concerns at a contract manufacturer. The recall covers a box containing one pre-filled syringe and one safety needle. Healthcare providers and patients should stop using the product immediately and follow the company’s guidance for disposal and refunds.
FDA analysis found undeclared sildenafil and tadalafil in Boner Bears Honey 100% Wildflower Honey. The recall covers 15-pouch boxes manufactured in Florida with distribution in New Jersey. Consumers should stop using the product and seek refund or replacement from Pure Vitamins and Natural Supplements.
Cipla USA, Inc. recalls lanreotide acetate 120 mg/0.5 mL pre-filled syringes distributed nationwide due to lack of assurance of sterility after FDA observations at the contract manufacturer. Health care providers and patients should stop use immediately and contact Cipla or their clinician for guidance.
FDA analysis found undeclared sildenafil in Red Bull Extreme Male Enhancement Supplement. The product, produced in Turkey and distributed in New Jersey, has Class I recall status. Consumers should stop use and contact the distributor for refunds or replacements.
One case of Treasured Harvest Chilli Spanish Peanuts, 25 lb bags, from Western Mixers Produce & Nuts was recalled after a glass fragment was found inside a sealed bag. The recall covers two consignees with 53 retail locations nationwide. Consumers should not consume this product and should contact the company for a refund or replacement via email.
Brahms GmbH recalled 5,254 units of the PlGF Plus KRYPTOR in vitro diagnostic test worldwide after reports of QC values out of range at QC Level 1. The issue may cause falsely elevated sFlt-1/PlGF ratios and higher risk classifications for preeclampsia progression. Stop using the device immediately and follow manufacturer recall instructions.