2,755 recalls tagged with “immediate action”.
Pocas International recalled 370 cases of Popping Boba RTD Peach Oolong Tea sold in NY, VA, FL, MA, TX, LA, UT, CA and Canada. A packaging integrity issue may compromise product quality. Consumers should not consume the product and should contact Pocas International Corp. for refund or replacement via email.
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.
17,056 units of Favorina Chocolate Ladybugs German-Style Nougat from Lidl US Trading are recalled. The recall covers products distributed to DC and 10 states. The label does not specify the type of tree nut contained.
Western Mixers Produce & Nuts recalled 384 cases of First Street Chilli Spanish Peanuts after a glass fragment was found inside sealed containers. The recall covers two consignees and 53 retail locations nationwide. Consumers should not eat the product and should email the company for refund or replacement.
Stryker Sustainability Solutions recalled 56,740 color cuff tourniquet cuffs due to potential detachment from the bladder. The recall affects 18" and 24" cuffs across multiple U.S. states. Patients and healthcare providers should stop using these devices immediately and follow manufacturer instructions.
17 Stories Furniture recalled its 14-drawer dressers on March 12, 2026, due to serious tip-over hazards. The dressers, sold in black, white, and brown, can pose risks of injury or death to children if not anchored. Model numbers include 55SCDR14KDBRDL and 55SCDR14KDCHDL.
LIVEHOM recalled 11-Drawer Dressers on March 12, 2026, due to tip-over hazards. The recall affects dressers sold on Amazon that can pose serious risks to children. Consumers must stop using these dressers immediately and contact the company for a full refund.
LFTE USA recalled Playground Swing Set Seats on March 12, 2026. The swing seats pose a fall hazard due to potential rivet failure. The recall affects model number 999604 with the code 'LF-65708' marked on the seat pad.
ProRider recalled several models of bicycle helmets on March 12, 2026, due to a serious risk of head injury. The helmets do not meet mandatory safety standards and can fail in a crash. Consumers should stop using these helmets immediately and seek a refund.
Stoney Games recalled Kluster Fun Tabletop Magnet Chess Games on March 12, 2026, due to a serious ingestion hazard. The games contain loose, high-powered magnets that can be swallowed by children, posing a risk of severe injury or death. Consumers should immediately stop using the games and contact Stoney Games for replacement options.
Honda recalls 2023-2025 Pilot and 2023-2024 Passport vehicles due to potential fuel filler neck tube and pipe separation. The defect can allow fuel leaks with a fire risk. Owners should contact Honda for inspection and repair at no cost. Recall OKM is in effect; letters mailed January 7, 2025.
Lone Star Dairy Products LLC issued an active recall of 1.79 million pounds of spray dried dairy powder sold in the United States after Salmonella spp. was identified in finished product testing. The affected product is packaged in 25 kg bags or 1 metric ton totes. Consumers should not consume the product and should contact Lone Star Dairy Products LLC for refund or replacement information via e‑m
Fresenius Kabi USA, LLC recalls 5% Dextrose Injection, USP IV solution in freeflex bags due to lack of assurance of sterility. The recall affects batches 6402399, 6402400, and 6402401 with Exp 02/28/2027. Distributors nationwide, including Alaska and Puerto Rico, are notified. Stop using and contact the company for guidance and potential replacement.