292 recalls tagged with “toddler product”.
Sno Pac Foods recalled 4,006 cases of Frozen Organic Spinach sold under Sno Pac Frozen Vegetables and Maika'i Keep Frozen. The spinach may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact Sno Pac Foods for refund or replacement.
Great Lakes Cheese Co Inc recalls 4,298 cases of pizza-style shredded cheese blends sold through retailers nationwide after metal fragments were found in supplier raw material. The defect involves potential metal fragments that could contaminate the cheese. Consumers who may own any of the affected products should not consume them and should contact Great Lakes Cheese Co for refund or replacement.
Great Lakes Cheese Co recalls 4,131 cases of mozzarella and provolone shredded cheese blends sold under four store brands due to metal fragments from supplier raw material. The hazard involves potential metal fragments detected in the shredded cheese products. Consumers should not consume these products and should contact Great Lakes Cheese Co for refund or replacement information.
Coca-Cola Southwest Beverages LLC recalls 1,115 units of Coca-Cola Zero Sugar 12oz cans sold in Texas. The cans may contain metal fragments. Consumers should not drink the product and should contact the company for refund or replacement.
Coca-Cola Southwest Beverages recalled 791 Sprite 12oz cans sold at retailers in Texas after metal fragments were found in the product. The recall concerns Sprite 12oz cans in 35-pack and 12-pack formats. Consumers should not drink the product and should contact Coca-Cola Southwest Beverages LLC by email for refunds or replacements.
In Motion Design recalled Evermore Surprise Eggs due to lead content above federal limits. The recalled eggs were sold with yellow, pink or green wrap and include a gold egg containing seven toys, including a toy airplane. Consumers should stop using the product and return it for a full refund.
Blossom recalled two-piece children’s loungewear sets sold under its brand due to a burn risk that violates the mandatory flammability standard for children's sleepwear. The recall covers sets in multiple colors and designs sold for sizes 12 months through 12 years. Stop using the garments and contact Blossom for a full refund.
AFCO's hand sanitizer 5515 is being recalled nationwide through distributors and retailers. The recall cites cGMP deviations that left methanol risk unexcluded. Consumers and healthcare providers should stop using this product immediately and contact Acuity Specialty Products for guidance.
Albertsons Companies is recalling Ready Meals Smoked Mozzarella Penne Pasta Salad sold under Carrs-Safeway, Eagle and Safeway banners in Alaska and 14 other states after the FDA linked the product to Listeria monocytogenes. The in-store Penne pasta ingredient recall prompted the action. Consumers should not eat the product and should contact Albertsons Companies LLC for refund or replacement.
Wholesale Produce Supply LLC recalled 307 cases of cantaloupe chunks sold under Fresh & Finest, Harvest Cuts and other labels. The recall targets a broad range of container sizes and UPCs in IA, IL, ND, NE and WI. The recall cites potential Listeria monocytogenes contamination and is classified as Class I.
Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Tray with Strawberries after potential Listeria monocytogenes contamination. The recall covers trays packed in Minneapolis, MN and distributed to Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The product should not be consumed and refunds or replacements are being offered. The recall is active as of the latest notice.
Synthes USA recalled 122 locking intramedullary nail screws used in RFN-Advanced and Tibial Nail Advanced systems. The recall covers worldwide distribution including the US and Canada. The packaging labeling misstates screw length while the etched length on the screw is correct. Healthcare providers should stop using the device immediately and follow recall instructions from Synthes.
Wegmans Food Markets recalled 521 units of Wegmans Large Ultimate Strawberry Topped Cheesecake distributed in Virginia, Maryland, North Carolina and Washington, D.C. The cake contains undeclared pecans, posing an allergen risk. Consumers should not eat the product and should contact Wegmans for a refund or replacement.
A high-risk recall affects 795 cases of Reser’s Fine Foods Basil Pesto Bowtie Pasta Kit distributed in Arizona, California, Colorado, Utah and Washington. The recall covers item #404736 with use-by dates in October 2025. Consumers should not consume these salad kits and should contact Reser’s for refunds or replacements.
LeMaitre Vascular recalled 1 Artegraft AG1015 vascular graft distributed to Arkansas hospitals after a packaging size labeling error. The packaging error could lead to using the wrong size graft during surgery. Hospitals and patients should stop using the device and follow recall instructions. See the recall letter for instructions from LeMaitre Vascular or your healthcare provider.
NOW Foods recalled 1,689 10 oz pouches of NOW Real Food Organic Unsalted Whole Raw Cashews nationwide after undeclared pine nuts were detected. The hazard poses an allergen risk. Consumers who bought this product should stop using it and contact NOW Foods for a refund or replacement.
Kico Knee Innovation recalls 21 ARVIS Shoulder systems nationwide after reports that AI planning software may cause implant malalignment or reduced range of motion. The recall covers software version V2025.1.2 used with IN-27300 hardware. Healthcare providers and patients should stop using the device and follow manufacturer instructions.
Arizer recalled the Solo II portable vaporizer on 2025-09-18 after reports of overheating lithium-ion batteries. The recall targets units imported by 7111495 Canada. Consumers should stop using the device and pursue a free replacement.
Cardinal Health recalled Salem Sump dual-lumen stomach tubes worldwide after ARV breakage complaints. The anti-reflux valve can break when excessive force is used. Healthcare providers and patients should stop using the device and follow recall instructions from the manufacturer.
B Braun Medical recalled 10,130 ESPOCAN spinal/epidural trays nationwide after discovering potential for the catheter connector lid to be in an incorrect position. The recall covers multiple product codes and UDI numbers. Healthcare providers must stop using affected units and follow manufacturer instructions for remediation.