2,756 recalls tagged with “immediate action”.
Sheathing Technologies recalled 12 units of its ultrasound probe covers on November 17, 2025, due to potential contamination risks. The non-sterile vaginal and rectal covers may have defects that pose an infection risk during use. Consumers should stop using the product immediately and follow the manufacturer's instructions.
Molift recalled 71 Mover 300 mobile hoists on November 17, 2025, due to a potential bolt failure. The defect can lead to limited mobility, posing a high risk to users. Affected models include M1501, M1502, M1504, among others.
ETAC A/S recalled 25 units of the Molift 4-point sling bars on November 17, 2025, due to a defect that can lead to improper functionality. The issue stems from a bolt that may break during assembly and load testing, posing a high risk during use. This recall affects products distributed worldwide, including the United States and several European countries.
ETAC A/S recalled 95 Molift Mover 205 devices due to a serious defect. The lifting bar bolt can break during use, posing a high risk of injury. Customers should stop using the product immediately and contact the company for further instructions.
ETAC A/S recalled 64 units of Molift 2-point sling bars on November 17, 2025. A defect in the mounting bolt can lead to failure during use. This poses serious risks for users relying on the device for mobility assistance.
Prime Food Processing LLC recalls Lava Bun with Salted Egg Yolk sold at multiple retailers nationwide after undeclared milk was found in the product. The issue centers on missing milk declarations in the Contains and ingredient statements. Consumers should not eat the product and should contact Prime Food Processing for a refund or replacement.
Prime Food Processing recalled 2,243 cases of Lava Bun with Green Tea Flavor sold across 33 states. Milk is not declared in the contains or ingredient statement. Consumers should not consume this product and contact Prime Food Processing for refund or replacement.
Charlevoix Cheese Company recalled 420 units of Mild Cheddar Cheese on November 16, 2025. The recall stems from a possible Listeria monocytogenes contamination. Consumers should not consume the product and should seek refunds immediately.
Cipla USA, Inc. recalled 63,504 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall results from a nitrosamine impurity, N-nitroso-cinacalcet, exceeding acceptable daily intake limits. Consumers should stop using the tablets immediately and contact healthcare providers for guidance.
Venzu Traders LLC recalled 24 cases of cinnamon powder on November 14, 2025, due to potential lead contamination. The affected product weighs 3.5 ounces and is sold under UPC 7 46241 29537 8. Consumers should stop using this product immediately and contact the distributor for a refund.
Olympus Corporation of the Americas is recalling 1,684 ShockPulse-SE Lithotripsy System generators worldwide, including SPL-G models. Investigations found the generator can blink and fail to recognize the transducer, and damage to the transducer plug or generator receptacle may occur. Healthcare providers and patients should stop using the device immediately and follow recall instructions provided
Cipla USA recalled 12,576 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025, due to a nitrosamine impurity. The impurity, N-nitroso-cinacalcet, exceeds acceptable daily intake limits. Consumers must stop using this product immediately and contact healthcare providers for guidance.
Face Rock Creamery recalled 16 units of Vampire Slayer Garlic Cheddar Cheese, 6 oz, distributed in Oregon after an FDA environmental sample detected Listeria monocytogenes in the packaging area. The hazard is a contamination risk that could cause life-threatening infection in some populations. Consumers should not eat the cheese and should contact Face Rock Creamery for a refund or replacement.
Cipla USA, Inc. recalled 15,744 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall follows the discovery of a nitrosamine impurity exceeding acceptable daily intake limits. Consumers should stop using the product immediately and consult healthcare providers.
Olympus Corporation of the Americas is recalling 1,082 ShockPulse Lithotripsy System SPL-S single-use probes worldwide. Investigations found the device’s generator may blink and fail to recognize the transducer, risking damage to the transducer plug or generator receptacle. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus.
Olympus Corporation of the Americas recalls 602 ShockPulse-SE Lithotripsy System reusable probes worldwide to hospitals. The recall cites a blinking generator that may fail to recognize the transducer and damage the transducer plug or generator receptacle. Hospitals and patients should stop using SPL-SR probes immediately and follow manufacturer recall instructions.
Zigjoy-US recalls Zigjoy-branded children's sleep sacks sold online after risk of serious burn injury. The recall covers blue sleep sacks with an excavator print and pink with a bunny print in sizes S, M, and L. The products claim 100% cotton on sewn-in labels. Consumers should stop using them immediately and seek a full refund.
American Nuts recalls 2,700 units of Dry Roasted Macadamia Nuts, Unsalted Halves distributed to two consignees in Hawaii after a potential Salmonella contamination. The product has UPC 8 60011 44301 8 and Lot Code 307HMNC25L3. Stop consuming the product and contact American Nuts, LLC by telephone for a refund or replacement.
Microbiologics recalled 5 KWIK-STIK quality control kits for culture media after发现 some kits labeled for lot 818-111-7 were packed in pouches marked as lot 857-53-10. The mislabeling could affect quality control results for Vibrio parahaemolyticus tests derived from ATCC 17802. Laboratories and healthcare facilities should stop using the kit and follow the manufacturer’s recall instructions.
Trek and Electra recall certain bicycles and replacement rear wheels sold by Trek authorized retailers and Trek.com due to a crash hazard. The coaster brakes can fail to engage, increasing the risk of loss of rider control. Consumers should stop riding recalled bikes, check serial numbers starting with WTU located under the bottom bracket, and contact a Trek or Electra dealer to schedule a free, 3