1,215 recalls tagged with “replacement available”.
Burlington Medical recalled 961 caps used in medical devices sold to healthcare providers worldwide. The caps may experience attenuation degradation over time, shortening device lifespan. Healthcare providers and patients should stop using the affected caps and follow recall instructions.
Burlington Medical recalled 41,962 Thyroid Shield units worldwide after identifying attenuation degradation that could shorten the device’s lifespan. The attenuation material may degrade over time, reducing shielding effectiveness. Patients and healthcare providers should stop using the device immediately and follow the recall instructions in the manufacturer notice.
Medline recalled 108,971 units of Puracol MSC8522 and Puracol Plus MSC8622EP collagen wound dressings nationwide in the United States, with distribution to Mexico and Panama. Elevated endotoxin levels were identified in affected lots. Stop using the dressings and follow recall instructions provided by Medline or your healthcare provider.
Orthalign recalled 7 drill plates used with its Lantern Knee System distributed nationwide, including Utah. The parts were manufactured out of specification and can cause a bone cut up to 0.008 inch (2.8448 mm). Healthcare providers were notified by letter and instructions to stop using the devices.
Orthalign recalled 7 pegged drill plates used with the Lantern Knee System due to out-of-spec manufacturing that can cause bone cuts up to 2.8448 mm. The devices were distributed in Utah and across the United States. Healthcare providers and patients should stop using the device immediately and await recall instructions by letter.
Boston Scientific is recalling 806 EndoVive Safety PEG Kits sold nationwide. The recall concerns BD ChloraPrep Triple Swabsticks with open or compromised seals that could compromise sterility or dry the antiseptic solution. Hospitals and patients should stop using the kits immediately and follow the manufacturer's recall instructions.
Trividia Health recalled 1,001,534 TRUE METRIX PRO owner’s booklets used with glucose meters distributed worldwide through multiple retailers. The labeling fails to clearly warn that an E-5 error could indicate very high blood glucose and does not emphasize immediate actions. Consumers should stop using the device and follow manufacturer recall instructions by letter, contacting Trividia Health or
International Life Sciences issued an active recall of Artelon FLEXBAND TWIST augmentation devices. The devices were distributed worldwide, including nationwide in the United States. The recall concerns failures in bacterial endotoxin testing that could pose a infection risk; users should stop using the device and follow recall instructions from the manufacturer.
Trividia Health's TRUE METRIX GO blood glucose kits sold at Walgreens, CVS and other retailers are recalled worldwide. The labeling fails to clearly emphasize that an E-5 error could indicate very high blood glucose and require immediate action. Consumers should stop using the device and follow manufacturer guidance.
International Life Sciences recalled Artelon FlexBand Dynamic Matrix 31057 after endotoxin testing failures. The recall covers the augmentation device used in medical procedures. Patients and healthcare providers should stop using the device immediately and await manufacturer instructions.
International Life Sciences recalled Artelon FlexBand Plus augmentation devices after endotoxin testing failures. The recall affects devices with REF 41054 and REF 41057 distributed worldwide. Patients and healthcare providers must stop using the devices immediately and follow manufacturer instructions for recall return.
Dresbe LED Christmas Headbands are recalled in 2026 after a battery ingestion hazard was identified. The recall covers a two-pack set labeled HB-052. Stop using the headbands and contact Dresbe for a full refund.
Lola Plus The Boys recalls five youth hooded clothing styles sold nationwide and online at Lolaandtheboys.com from November 2022 through September 2025. Drawstrings with beads on the recalled garments can snag on objects and pose a strangulation risk. Stop using the recalled clothing now and contact Lola Plus The Boys to obtain a full refund.
Little Cow Company LLC recalled 9 oz glass jar candles sold at New Seasons Market and Town & Country stores nationwide from December 2025 through January 2026 for about $25. A glass jar may crack or break during use, creating a fire, burn and laceration risk. Stop using the recalled candles and contact Little Cow Company for a full refund.
Aterian recalls PurSteam Elite Travel Steamers and PurSteam Mighty Lil Steamers sold after December 2020 due to a burn risk. The steamers can expel hot water from the steam nozzle during use. Affected consumers should stop using the recalled steamers and submit a recall request at recall.pursteam.com for a full refund, which requires cutting the cord and uploading a photo of the steamer with its C
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.
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.