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

Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.

Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that may result in failure of the AIC to recognize the purge cassette during case setup or cassette change. This issue may result in delay in procedure or therapy. 2. Potential for the rotary push button (RPB) sticking and unreliable actuation impacting operator ability to select and confirm menu entries. This can result in loss of control of the console. 3. Potential AIC instability that could result in AIC start-up failure, inability to drive the pump, and the need for console exchange. 4. Software defect related to calculator process crash, leading to Negative Central Venous Pressure (CVP) values present in Pulmonary Artery Pressure (PAP) calculations.

Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that may result in failure of the AIC to recognize the purge cassette during case setup or cassette change. This issue may result in delay in procedure or therapy. 2. Potential for the rotary push button (RPB) sticking and unreliable actuation impacting operator ability to select and confirm menu entries. This can result in loss of control of the console. 3. Potential AIC instability that could result in AIC start-up failure, inability to drive the pump, and the need for console exchange. 4. Software defect related to calculator process crash, leading to Negative Central Venous Pressure (CVP) values present in Pulmonary Artery Pressure (PAP) calculations.

Software problem has the potential for an inaccurate displayed longevity estimate.

Due to software issue, X-ray interventional system may experience internal error if F-Store or imagine acquisition is performed while clinical analysis function is use.

Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.

Retrospective review of servicing records identified AIC units requiring various hardware, firmware, and/or software update(s): 1. RFID firmware issue that may result in failure of the AIC to recognize the purge cassette during case setup or cassette change. This issue may result in delay in procedure or therapy. 2. Potential for the rotary push button (RPB) sticking and unreliable actuation impacting operator ability to select and confirm menu entries. This can result in loss of control of the console. 3. Potential AIC instability that could result in AIC start-up failure, inability to drive the pump, and the need for console exchange. 4. Software defect related to calculator process crash, leading to Negative Central Venous Pressure (CVP) values present in Pulmonary Artery Pressure (PAP) calculations.

Affected leads require additional engineering evaluation due to complaints regarding difficulty in achieving fixation during implantation. Potential harm of tissue trauma due to implant difficulty.

Spencer Manufacturing, Inc. (Spencer) is recalling certain 2026 Rescue, 2025 Initial Attack, and 2024-2025 Pumper emergency vehicles. The display may stop responding to touch commands or fail to power on, preventing the activation of exterior emergency lights, fire fighting and other emergency equipment. A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing the risk of injury.

Hyundai Motor America (Hyundai) is recalling certain 2019-2022 Veloster N, 2019-2023 Kona Electric vehicles. A software error in the air bag control unit (ACU) may improperly deactivate the air bag system and seat belt pretensioners. Air bags and seat belt pretensioners that do not activate in a crash increases the risk of injury.

WASHINGTON, Sept. 25, 2026 – Fontanini Foods LLC, a McCook, Ill., establishment, is recalling approximately 2,320 pounds of raw, frozen pork breakfast sausage products that may be contaminated with foreign material, specifically clear, hard plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The raw, frozen pork breakfast sausage items were produced on June 23, 2026. The following products are subject to recall [ view labels ]: 10-lb. cardboard box cases containing “Fontanini PORK SAUSAGE LINKS” with “ITEM 393” printed on the box and “PACKED ON 06/23/2026” printed on the shipping label. The products subject to recall bear establishment number “EST. 6944” inside the USDA mark of inspection printed on the box. These items were shipped to distributors in California, Florida, Michigan, and Nevada to be served in food service establishments, including restaurants. The problem was discovered after the firm received two customer complaints regarding clear, hard plastic found in the sausage product. There have been no confirmed reports of injury or adverse reactions due to consumption of these products. Anyone concerned about an injury should contact a healthcare provider. FSIS is concerned that some product may be in food service and restaurant freezers. Food service establishments and restaurants are urged not to serve this product. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify theircustomers of the recall and that steps are taken to make certain that the product is no longer available to consumers. If any specific retail locations are identified, a distribution list will be posted on the FSIS website at www.fsis.usda.gov/recalls . Consumers, foodservice operators, and members of the media with questions about the recall can contact Fontanini Foods 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/ .

WASHINGTON, Aug. 7, 2026 – Corte Argentino USA LLC, located in Aventura, Fla., is recalling approximately 29,628 pounds of raw beef products that were imported from Argentina without the benefit of import reinspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The raw beef products were produced between May 15, 2026, and May 20, 2026, and have use or freeze-by dates between September 15, 2026, and September 20, 2026. The following products are subject to recall [ view labels ]: Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Top Sirloin Butt” (“Cuadril Sin Tapa”) Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Eye Round” (“Peceto”) Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Topside Cap Off” (“Nalga AD S/Tapa”) Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Flat” (“Carnaza Cuadrada”) Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Knuckle” (“Bola de Lomo”) The products subject to the recall bear Argentinian establishment number “EST. N° OF. 2025” and shipping mark “26644-AA” The products were distributed to distributors and retailers in Florida and Texas. The problem was discovered during routine FSIS inspection activities. There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider. FSIS is concerned that some product may be in consumers’ refrigerators and 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 theircustomers 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 . Consumers and members of the media with questions about the recall can contact Eial Kaplun, General Manager, Corte Argentino USA LLC, at 786-350-5805 or [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/ .

WASHINGTON, JULY 23, 2026 - BCI Foods, Inc., the importer of record located in Saint-Hyacinthe, Quebec, Canada, is recalling approximately 4,300 pounds of a chicken noodle soup product that was imported from Canada without the benefit of import reinspection into the United States, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today. The canned condensed chicken noodle soup product was produced on February 4, 2026. The following product is subject to recall [view labels ]: 10.5-oz can of "tasty KITCHEN Chicken Noodle Condensed Soup PRODUCT OF CANADA" with best by date of "2028 FE 04" and lot code "5 9 2 26 035" The product subject to recall bears Canadian establishment number "EST. 142" printed on the can. This item was further distributed to food banks and food pantry locations in Oklahoma. The problem was discovered when the firm notified FSIS that the canned chicken soup product imported from Canada was not presented for FSIS import reinspection. There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider. FSIS is concerned that some product may be in consumers' pantries. 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 . Media and consumers with questions regarding the public health alert can contact Marie-Lou Corbin, Vice President, Sales, BCI Foods, Inc., at 514-218-7143 or [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/ .

Mack Trucks, Inc. (Mack) is recalling certain 2024-2026 Medium-Duty Electric (MDe) vehicles that were incorrectly manufactured with the hill start assist (HSA) message enabled. A false hill start assist message can lead to unexpected vehicle rollback on an incline, increasing the risk of a crash.

General Motors, LLC (GM) is recalling certain 2023–2027 Cadillac LYRIQ, 2025–2026 model year Cadillac CELESTIQ, 2024–2027 Chevrolet Blazer EV, and 2026-2027 Cadillac VISTIQ vehicles. The brake system control module (BSCM) contains a software defect that may cause a loss of braking during certain driving conditions. A loss of braking ability increases the risk of a crash.

General Motors, LLC (GM) is recalling certain 2025-2026 Chevrolet Express and GMC Savana vehicles. The steering gear assembly may have a nut that was not properly tightened. A loose nut that separates from the steering gear assembly while driving can cause a loss of steering control, increasing the risk of a crash.

This recall involves Jocoevol 6-Drawer Dressers. The recalled dressers come in black, pink, brown and white colorways. The dressers have six drawers and are made from engineered wood. They are 47.2 inches wide, 15.3 inches long, 32.3 inches tall, and weigh 97 pounds. The dressers have the model number “C-0633” printed on a label inside the top left drawer.

This recall involves Whatever Works microwave grillers. The rectangular grills have a white plastic exterior with black locking clips on the side, hinge tabs at the rear, and two non-stick black metal plates. Model K4001 can be found on the product’s purchase receipt.

This recall involves HAIARA power banks, model W5 PRO, sold on Amazon.com by Mitrytech. The power banks are black and have “20W” printed on the front and “Model: W5 PRO” printed on the side. The seller name, Mitrytech, and brand name, HAIARA, are located on the purchase receipt. This warning applies to power banks with no date code (formatted “YYYYMMDD”) printed on the side.

This recall involves SOOWERY 8-Drawer Fabric Dresser. The recalled dressers come in gray and black. The dressers have eight fabric drawers and the frames are made of metal. They measure 47.2 inches wide, 11.8 inches long, 35.4 inches tall and weigh 47.5 pounds. The SKU “SOO-8DD-G01” is printed on the products packaging.

This recall involves three RootStim Minoxidil Hair Regrowth Treatment bottles: RootStim 5% Minoxidil Foam Hair Regrowth Treatment with Rosemary and Biotin, 6 fl. oz. The Foam comes in a blue and white package, with an orange accent band or orange lettering. The package contains three 2 fl. oz. pump-foam bottles. UPC code 810169130594 is printed on a label on the bottom of the box. RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil Rosemary & Biotin, 2 fl. oz. The spray comes in a magenta box with a 2 fl. oz spray-pump bottle. UPC code 810169301005 is on a label on the bottom of box. RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil with Rosemary, 4 fl. oz. The serum comes in a blue and white package with an orange accent band containing two 2 fl. oz. amber glass bottles with black spray-pump caps. UPC code 810169301012 is on a label on the bottom of the box.

This recall involves PILLANI-branded nursing pillows. The U-shaped nursing pillows were sold in the following colors and prints: cloud and stars, wild animal, white with leaf and feather, stars, pink with leaf, light blue, pink, light yellow, gray, light gray, beige and light green. The pillows have a smaller pillow attached atop and an adjustable waist strap. The brand name, model number NP4351 and batch numbers 202604, 202605 or 202606 are printed on an attached label.

This recall involves NTI brand residential gas boilers in the FTVN and TFTN model series, and HTP brand residential gas boilers in the EFTU model series. The NTI FTVN and TFTN series boilers are gray, while the HTP EFTU (Elite Fire Tube Ultra) boilers are black. The boilers are metal, rectangular units and have either NTI or HTP printed on the front. The model serial number can be found on the rating plate, located on the left-hand side of the boiler. The following models and serial number ranges are included in this recall:

This recall involves Pamag Pieeoo Mattresses. The mattresses are 8 inches thick and were sold in a twin-XL size. They have a white top and white sides with a gray curve pattern. They were sold compressed in a box. The date of manufacture and “Model: BFC8HMBYTX-US” and care instructions are printed on a sewn-in white label located on one side of the mattress.

This recall involves QZH.DUAO pajama sets. The pajama sets consist of short-sleeve tops and matching pants. They were sold in Pink Bow, Pink, Black, Light Blue, Purple, Mint Green, Hot Pink, Pink Bowknot, Blue Bowknot, Pink Strawberry and Pink Bow Flower and in sizes 4-5T through 13-14 years.