794 recalls tagged with “infant product”.
Ajinomoto Foods North America recalls 537,033 pounds of Ajinomoto Green Gyoza Vegetable & Edamame Dumplings sold nationwide after glass fragments were found. Glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the recalled dumplings and should contact Ajinomoto Foods North America for a refund or replacement.
K.C. Pharmaceuticals recalled 315,144 sterile eye drop bottles distributed nationwide after lack of sterility. The products span several brands including GNP Eye Drops Redness and Dry Eye Relief, Leader Eye Drops Redness Relief, and Foster & Thrive Redness Relief Eye Drops. Consumers should stop using the products immediately and follow guidance from KC Pharmaceuticals or their healthcare provider
More than 1.02 million bottles of Dry Eye Relief Eye Drops across multiple brands were recalled nationwide on March 3, 2026. The products were distributed by KC Pharmaceuticals and sold at retailers including Rite Aid, Meijer and H-E-B. The FDA notice cites a lack of assurance of sterility as the reason for the recall. Stop using these products immediately and contact KC Pharmaceuticals for next‑s
Philips Medical Systems Nederland B.V. recalled 15 Allura Xper FD10C radiography systems worldwide, including 7 in the United States and 8 overseas. The devices may fail to initiate X-ray imaging or intermittently stop imaging when using the wired foot switch. Facilities should stop using the devices and await recall instructions from Philips.
Civco Medical Instruments recalled 10 eTRAX Needle Sensor 16G units for Aurora Trackers. An inspection and programming error could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.
Civco Medical Instruments Co. is recalling 5 eTRAX Needle Sensor 14G units for Aurora Trackers. The recall cites a programming and inspection error that could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.
CNC Noodle Corp. recalls 427 cases of Steam Noodles distributed in California and Nevada after undeclared wheat was found. The recall cites wheat allergy risks for consumers and advises refunds or replacements. The recall was issued 2026-03-02 and remains active.
Philips Respironics recalls 113,717 Trilogy Evo O2 home-use ventilators in 2026. The Obstruction Alarm may fail to trigger within required standards, delaying warning for airway obstruction for up to four breaths. Stop using the device and follow recall instructions from Philips or your clinician.
Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold in the United States and internationally after determining the Obstruction Alarm may fail to trigger within required standards. The alarm can delay alerting caregivers for up to four breaths. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Philips or their clinician.
CNC Noodle Corporation recalls 310 cases of fresh noodles sold in California and Nevada after undeclared wheat and Yellow Dye 6 are found. The recall is classified as Class II and is active as of March 18, 2026. Consumers should not eat the product and should seek a refund or replacement from CNC Noodle Corporation.
Medline Industries, LP recalls 3,120 medical convenience kits worldwide due to a risk the syringe rotating adaptor may unwind during use. The issue can create a loose connection or complete disconnection between the syringe and manifold. The recall was issued on February 27, 2026 and is active. Customers should stop using the kit and follow manufacturer instructions for recall notices.
4,611 bottles are recalled nationwide. The product is Savannah Bee Company Honey BBQ Sauce Mustard, distributed to numerous states. The bottle actually contains Honey BBQ Sauce 'Sweet' which contains wheat and soy not declared on the Mustard label. Stop using the product and contact Savannah Bee Company for a refund or replacement.
Medline Industries issued a Class I recall for 79,843 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The action covers worldwide distribution including the US and PR. The risk is a syringe adaptor unwinding during use, which may cause a loose connection or disconnection with the manifold. Stop using the device immediately and follow recall instructions.
Medline Industries recalls 192,690 Angiographic Control Syringes worldwide after post-market surveillance found a rotating adaptor may unwind. The defect can cause a loose or complete disconnection between syringe and manifold. Stop using immediately and follow recall instructions.
Spacelabs Healthcare recalled the Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor, distributed worldwide. A circuit board issue in Auto mode may trigger CO readings improperly, causing Bad Curve or Irregular Curve errors. Stop using immediately and follow manufacturer instructions.
Medline Industries, LP recalls 17,902 medical convenience kits worldwide after post-market surveillance found a potential risk of the syringe rotating adaptor unwinding. The recall covers NAMIC Angiographic RA control syringes labeled in 10 Medline SKUs. Healthcare providers should stop use immediately and follow recall instructions.
Medline Industries, LP recalls 762 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes sold worldwide, including the U.S., PR, Canada, and several international markets. The recall cites a potential risk that the syringe rotating adaptor may unwind during use, creating a loose connection or disconnect between the syringe and the manifold. Stop using the device and seek
Medline Industries, LP recalled 439 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans worldwide distribution including the US, Puerto Rico, and multiple international markets.
Medline Industries, LP recalled 60 medical convenience kits worldwide due to a potential rotating adaptor unwinding in NAMIC Angiographic RA control syringes. The issue may cause a loose connection or disconnection between the syringe and manifold. Healthcare providers should stop using the device and follow the manufacturer’s recall instructions.
Medline Industries, LP recalls 1,698 medical convenience kits worldwide over a potential unwind of the NAMIC Angiographic Rotating Adaptor during use. The risk could cause a loose connection or complete disconnection between the syringe and manifold. Healthcare providers and patients should stop using the affected kits immediately and follow recall instructions.