378 recalls tagged with “kitchen”.
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 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.
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.
TG Foods recalled 7,980 units of Divided Sunset Multi Collagen Peptides 8 oz stand-up pouches distributed nationwide. The recall notes the ingredient statement lists wild caught marine collagen and eggshell membrane collagen but does not declare EGG or the specific fish species. Consumers should not consume the product and should contact TG Foods for refund or replacement information.
Olympus recalled 32 SOLTIVE Pro SuperPulsed Laser System units distributed worldwide after a defect in the 24V power supply may render the device inoperable. The defect can cause smoke or a burning smell, but the issue is contained within the laser console enclosure and self-extinguishing. Stop using the device and follow the manufacturer’s recall instructions.
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, 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 2,154 medical convenience kits worldwide after post-market surveillance found a risk that the NAMIC Angiographic Rotating Adaptor may unwind. A loose connection or disconnection between the syringe and manifold could occur. Stop using immediately and follow manufacturer recall instructions.
Medline Industries, LP recalls 1,752,096 NAMIC Angiographic Syringe kits worldwide, including the US and Canada. The recall stems from a post-market signal about the rotating adaptor unwinding during use. This may cause a loose connection or disconnection between the syringe and manifold. Health care providers and patients should stop using the devices and follow recall instructions.
Medline Industries, LP recalls 2,980 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans the United States, Puerto Rico and multiple international countries. The rotatable adaptor may unwind during use, risking a loose connection or disconnection between syringe and manifold. Patients and healthcare providers should stop using the device and followMed
Medline Industries, LP recalls 20 kits worldwide after post-market surveillance found a risk the syringe rotating adaptor may unwind during use, causing a loose connection or full disconnection with the manifold. The recall affects three Medline SKUs and includes UDI details and lot numbers. Healthcare providers and patients should stop using the device immediately and follow Medline's recall plan
American Laboratories recalled 468 kg of Pepsin 1:3000 Powder distributed through 11 wholesale accounts in the United States and one in Australia. The powder is potentially contaminated with Salmonella and could cause illness if used. Consumers who purchased this product should not consume it and should contact American Laboratories by email for refund or replacement.
American Laboratories recalled 370 kg of Pepsin 1:10,000 Powder sold through 11 wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one account in Australia after a potential Salmonella contamination. The product carries a possible Salmonella contamination risk. Consumers should not consume the product and should contact American Laboratories for refund or replacement via email.
American Laboratories recalled 400 kg of Pepsin Full Strength Powder sold to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one wholesale account in Australia after a recall cited potential Salmonella contamination. The product is Item #5000545 and packed in double poly-lined drums or boxes. Consumers should not consume this product and should contact American Laboratories,
Olympus recalls 7 PKS Cutting Forceps worldwide because welded components may fail. The devices are used with a 5mm cannula and an electrosurgical generator. Stop using the device and follow the manufacturer’s recall instructions. Healthcare facilities should verify device details and consult Olympus for replacement options.
Uncle Ray's recalled 2,800 cases of Lowes Foods Sour Cream and Onion potato chips sold in North Carolina after detecting inaccurateNutrition Facts and undeclared ingredients. The 8-ounce bags carry UPC 7 41643 05576 6. The recall was issued February 25, 2026 and remains active. Consumers should stop using the product and contact Uncle Ray's for refund or replacement information.
A Tipp Distributors, Inc. dba Novamex recall affects 12,000 cases of C2O Coconut Water with Pulp sold across multiple states. The outer cardboard box lists an incorrect Nutrition Facts Panel and Ingredient List, omitting added sugar. The can itself has the correct information. Consumers should avoid consumption and seek refund or replacement.
King Harvest Balsamic Hummus recalled by Pacific Coast Fresh Co. The product was distributed in Oregon and Washington. A foreign material aluminum piece hazard was identified. Consumers should not eat the product and should contact Pacific Coast Fresh Co for refund or replacement information by telephone.
King Harvest Roasted Red Pepper Hummus, distributed in Oregon and Washington by Pacific Coast Fresh Co, is recalled. The recall cites foreign material aluminum pieces found in 10 oz and 17 oz tubs. Consumers should not eat the product and should contact Pacific Coast Fresh Co for a refund or replacement.
Pacific Coast Fresh CO recalls 348 10-ounce King Harvest Sundried Tomato Hummus containers sold in Oregon and Washington after aluminum pieces were found. The hazard is foreign material aluminum pieces in the hummus. Consumers should not consume the product and should contact Pacific Coast Fresh CO by telephone for refund or replacement.