1,862 recalls tagged with “stop use immediately”.
Fresenius Kabi Compounding recalled 10,548 bags of thiamine HCl injection on February 5, 2026. The recall follows a lack of assurance of sterility, posing a high health risk. Affected products include several lots expiring between February and May 2026.
Remel, Inc. recalled 97 units of Campy CVA Medium on February 5, 2026. Customers reported low to no recovery of Campylobacter Jejuni ATCC 33291 in the affected lot. Healthcare providers and patients must stop using the product immediately.
Andy & Evan recalled children’s pajama sets due to a burn hazard. The recall covers sizes 2T through 6X sold online and at multiple retailers from February 2024 through June 2025 for $13 to $58. Consumers should stop using the pajamas and seek a full refund.
Furnulem recalled its five-drawer dressers sold at multiple retailers after safety concerns linked to tip-over and entrapment risks. The dressers can be unstable if not anchored to the wall, posing serious injury or death risk to children. Consumers should stop using the recalled dressers immediately and contact Furnulem for a full refund.
EnHomee recalled its 10-Drawer Dressers sold on Amazon after determining tip-over and entrapment hazards. The recall also notes a violation of the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and contact EnHomee for a full refund.
Clark Associates recalled Lancaster Table & Seating powder-coated aluminum outdoor chairs and barstools in 3 models. The recall covers 180 item numbers and colors across arm chairs, side chairs, and barstools. Consumers should stop using the recalled chairs and contact Clark Associates for a full refund.
Zan International Trading recalls Lotus Joy Organic Sweet Birch Essential Oil bottles due to packaging that is not child-resistant. The product contains methyl salicylate and poses a poisoning risk to children if swallowed. Stop using the product now and return it for a full refund by contacting Zan International Trading.
IF Holding II recalls 1,375 cases of Tippy Toes Apple Pear Banana baby food distributed by Topco Associates LLC in Illinois. The product may contain patulin contamination. Consumers should not consume the product and should contact IF Holding II for a refund or replacement by letter.
Diagnostica Stago recalled 369 STA Liatest Free Protein S kits worldwide on 2026-02-04 due to potential out-of-range results. The defect may underestablish protein S levels in normal plasmas. Stop using immediately and follow the manufacturer’s recall instructions via email.
Scepter B62 dual-chamber fuel containers imported by Mameix Retail are recalled for a flash fire and child poisoning risk. The recall cites a lack of flame-mitigation devices and a non–child-resistant spout. Consumers should stop using the recalled containers and contact Mameix Retail for a full refund.
Mazda North American Operations recalled certain 2024-2025 CX-50 vehicles on February 3, 2026. The recall affects trailer hitches that may have loose bolts. A detached hitch can create a road hazard, increasing crash risk.
Ford recalled certain 2025 F-250, F-350, and F-450 vehicles on February 3, 2026. The steering column shifter may detach, preventing the driver from shifting into park. This defect increases the risk of vehicle rollaway and crash.
GE Medical Systems recalled 125 Imactis CT-Navigation System stereotaxic accessories distributed worldwide to healthcare facilities. The recall cites a potential mismatch between the simulated needle trajectory and the actual trajectory. Healthcare providers should stop using the devices immediately and follow the manufacturer's recall instructions.
Ford Motor Company recalled 2025 Explorers due to transmission valve body issues. The problem may cause unexpected vehicle movement, increasing crash risk. Owners received notification letters on April 11, 2025.
B. Braun Medical recalled 105,550 BBraun Medical 21G X4.4CM Winged INF devices worldwide, including Texas and Costa Rica. A dull or blunt needle tip may be difficult to advance or break. Healthcare providers and patients should stop using the device and follow the manufacturer's recall instructions.
B. Braun Medical recalls 51,300 units of its 21GA Winged Infusion Set, model 7M2802, distributed worldwide including Texas and Costa Rica. The device’s needle tip can be dull or break, making advancement difficult. Stop using the device immediately and contact the manufacturer or your healthcare provider for instructions.
Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.
B. Braun Medical is recalling 21,000 21GA Winged Infusion Sets (Single Pack) distributed worldwide, including Texas and Costa Rica, catalog 7A3842. The needle tip can be dull or blunt, may be difficult to advance, or break. Clinicians and patients should stop using the device and await manufacturer instructions.
Tandem Diabetes Care recalled 1,380 insulin infusion pumps distributed internationally in the Czech Republic and Slovakia after translation errors in the Czech user guide could cause unintended insulin delivery. The most significant error told users to verify the infusion set is connected to the body when it should be confirming it is not connected. Following this instruction could result in a hyp
Medtronic MiniMed recalled 26,851 MiniMed 780G insulin pumps sold worldwide, including the United States and Israel. Three software defects tied to updates 6.60, 6.61, and 6.62 could misdose insulin. Stop using the affected pumps and follow the recall letter for instructions.