Product Recall Checker: Search Recalls by UPC, Lot Code, Brand or Model

Altec Industries, Inc. (Altec) is recalling certain 2025-2026 AM Series Aerial Device vehicles. The emergency stop switch located at the turntable is inoperative when the upper controls interlock is active and allows the upper and lower controls to remain powered when the emergency stop is depressed. An inoperative emergency stop switch increases the risk of injury.

Chrysler (FCA US, LLC) is recalling certain 2026 Ram 2500 Pickup trucks. The trucks may be equipped with steering column control modules that can cause a loss of electronic stability control. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 126, "Electronic Stability Control Systems." A loss of electronic stability control increases the risk of a crash.

Chrysler (FCA US, LLC) is recalling certain Mopar engines with part numbers 68364632CB and 68412483AF. Debris inside the engine may cause engine failure, which can result in a loss of drive power and/or an engine compartment fire. A loss of drive power increases the risk of a crash, and a vehicle fire increases the risk of injury.

Editor’s Note: Mar. 9, 2026 – The product list in this release has been updated to reflect that products with the listed lot numbers, regardless of best-by date, are subject to the recall. View product list . View labels . WASHINGTON, March 3, 2026 – Ajinomoto Foods North America, Inc., a Portland, Ore., establishment, is expanding its Feb. 19, 2026, recall of frozen not ready-to-eat (NRTE) chicken products that may be contaminated with foreign material, specifically glass , the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The establishment is recalling approximately 33,617,045 additional pounds of various ready-to-eat (RTE) and NRTE chicken and pork fried rice, ramen, and shu mai dumpling products, for a combined total of 36,987,575 pounds subject to recall. This expansion includes 16 products produced between October 21, 2024, and February 26, 2026, under brand names Ajinomoto, Kroger, Ling Ling, Tai Pei, and Trader Joe’s. The products subject to recall bear establishment number P-18356, P-18356B, or P-47971 inside the USDA mark of inspection. The items were shipped to retail locations nationwide. Certain Ajinomoto items were exported to Canada and Mexico. The problem was discovered when the establishment notified FSIS that it received multiple consumer complaints involving glass found in product. Upon further investigation, the establishment determined that a vegetable source ingredient, specifically carrots, was the likely source of the glass contamination, which also impacted the additional products subject to this expanded recall. There have been no confirmed reports of injury due to consumption of this product. Anyone concerned about an injury should contact a healthcare provider. FSIS is concerned that some product may be in retailers’ or consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls . Members of the media with questions about the recall can contact Corporate PR at [email protected] or call (909) 477-4800. Consumers with questions about the recall can contact Consumer Affairs, Ajinomoto Foods North America, at (855) 742-5011 or email at [email protected] . Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected] . For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/ .

Contains undeclared egg, soy, and hazelnut

Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.

FDA analysis revealed the presence of undeclared sildenafil and Tadalafil

Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.

Potential Salmonella Contamination

Products contain banned sweetener: cyclamates.

FDA analysis revealed the presence of undeclared sildenafil

Products contain banned sweetener: cyclamates.

FDA analysis revealed the presence of undeclared sildenafil

Label declares cream cheese but does not declare milk

Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.

Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.

May be temperature abused, which may result in growth of Clostridium botulinum

Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.

Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve error with no CO measurement or Irregular Curve error with CO measurement not automatically excluded, which may result in inaccurate readings, or the need of additional readings, which may lead to delayed care and/or fluid overload.

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.