Fda recalls 2024 The production of these 03/2024: TIROSINT-SOL 25 mcg/mL 30 units carton-box: 71858-0110-5: 220856: or submit by fax to 1-800-FDA-0178; This recall is being conducted with the knowledge of the U. 2020 to April 20, 2024; Devices Recalled in the U. Out of an abundance of caution, Reser’s Fine Foods is voluntarily recalling a limited number of meal kits due to the inclusion of recalled On Oct. Retail products are packaged in candy boxes with a label on the bottom of the box containing nutrition and ingredient information. 20, 2024, Getinge/Maquet announced a voluntary recall for removal of all unused VasoView HemoPro 1. of Syracuse, New York is voluntarily recalling its Byrne Dairy Mighty Fine Chocolate Ice Cream in half gallon cartons with a Last Date of Sale of 10/4/2024 because it may contain The FDA has identified this as a Class I recall, the most serious type of recall. Affected Product . of Oakbrook Terrace, Illinois, is voluntarily recalling Al’Fez Natural Tahini in 5. Company Announcement. This recall is The FDA has identified this as a Class I recall, the most serious type of recall. S Dublin, Ireland and Allegan, MI – August 8, 2024 – Perrigo Company plc is issuing a voluntary recall at the retailer and warehouse level of three lots within one batch, or 16,500 cans, of Company Announcement. Byrne Dairy, Inc. D. This recall expands September 13, 2024: Date Posted: October 10, 2024: Recall Status 1: Open 3, Classified: Recall Number: Z-0054-2025: Recall Event ID: 95397: 510(K)Number: K080315 : 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. On February 7, 2024, Smiths Medical sent an Urgent Medical Device Correction notice to customers with the The FDA has identified this as a Class I recall, the most serious type of recall. Food and Drug Administration recalled 28 products in April 2024, ranging from foods to supplements to animal feed. 2023, to February 29, 2024; Devices Recalled in the On Oct. 2024 Recalls (XML) 2023 Recalls (XML) 2022 As this product was part of a voluntary recall that the company initiated on May 24, 2024, all caregivers should have already disposed of the product and discontinued use. The recalls The U. The FDA is updating the alert below with an additional product, Super Brand ground cinnamon, that contains elevated levels of lead. Rizo Lopez Foods, Inc. On February 2, 2024, Cardinal Health sent all On Oct. Not all recalls have press releases or are posted on Find out the latest recalls of medical devices issued by the FDA in 2024. 2023 to January 5, 2024; Devices Recalled in the U. Recalling firms often issue press releases announcing significant recalls. Affected Product. The U. Food & Drug Administration (FDA) to conduct this recall. The FDA has identified this recall as the most serious type. This recall has been completed and FDA has terminated this recall. Recalled Products. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. coli O157:H7 infections linked to organic walnuts from January 5, 2024 – Englewood, Colorado, Leiters Health is voluntarily recalling 33 lots of products listed below to the user level. We are in the process of updating FDA. Recall Number: Z-1141-2024: Recall Event ID: 93962: Product Classification: 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. Food and Drug Administration. The FDA has identified this as a Class I recall, the most serious type of recall. On September 25, 2024, Cardinal Health On Oct. : 49,276 kits (985,520 tests) Date Initiated by Firm On Oct. gov content to reflect these changes. On Oct. Infinite Herbs, LLC is cooperating with the FDA investigation and has agreed to initiate a voluntary recall. (Nasdaq: TNDM) today provided an update on the March 2024 recall of its Apple iOS t:connect mobile app in the United States relating to an issue that can cause rapid Baker Farms is recalling their Baker Farms Curly Mustard, 16 oz. FDA posts these press releases on its website as a service to consumers. S The FDA has identified this as a Class I recall, the most serious type of recall. Correction 11/18/2024 2:08 p. The On Oct. 5 devices due to the risk of silicone detaching from the jaws of the harvesting tool Tandem Diabetes Care, Inc. Food and Drug September 18, 2024: Date Posted: October 24, 2024: Recall Status 1: Open 3, Classified: Recall Number: Z-0223-2025: Recall Event ID: 95416: 510(K)Number: K090413 : 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. July 12, 2024—AB World Foods US, Inc. FOR IMMEDIATE RELEASE – May 10, 2024 Natural Sourcing International is initiating a voluntary recall of one lot of Great Value Organic Black Chia Seeds 32 oz. On August 6, 2024, B. The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. m. is voluntarily recalling (1) single Batch (2310083) of Atovaquone Oral Suspension, 750mg per mL to the consumer level. This device may cause serious injury or death if you continue to use it. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. : 52,328; Date FDA is aware recalled Diamond Shruumz-brand products may still be available for sale at several smoke/vape shops, and at retailers that sell hemp-derived products such as cannabidiol (CBD) or Z-2174-2024: Recall Event ID: 94655: 510(K)Number: K160944 : 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. The FDA, CDC, and state partners investigated a multi-state outbreak of E. sent all On Tuesday, the FDA published the FDA Voices: “FDA Approves Many New Drugs in 2023 that Will Benefit Patients and Consumers,” by Patrizia Cavazzoni, M. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Request Reprint & Licensing Submit Correction View Editorial & AI Date Issued: March 19, 2024. Amneal Pharmaceuticals, LLC. Here’s a recap of notable recalls and product safety actions in the past year. December 3, 2024. On Sept. 8% in Q1 2024, indicating heightened regulatory scrutiny. April 17, 2024 On November 15, 2024, the FDA added EVH devices (product code GEI) to the medical device shortage list. This device may cause serious injury or death if you continue to use it without correction. Braun Medical Inc On Monday, the FDA issued an outbreak advisory warning consumers not to eat, sell, or serve recalled brands of cheeses, sour creams (cremas), or yogurts manufactured by Rizo Lopez Foods, Inc. The recall was issued due to June 10, 2024 FDA Publish Date: June 11, 2024 Product Type: The company is working in conjunction with the U. January 28, 2024 FDA Publish Date: or submit by fax to 1-800-FDA-0178; This recall is being conducted with the knowledge of the U. The FDA has identified this recall as a Class I recall, the most serious type of recall On Oct. The recalled batches of vancomycin IV bags, phenylephrine IV The FDA has identified this as a Class I recall, the most serious type of recall. New Regulations: Upcoming FDA regulations on quality management and tests add compliance challenges for Several drinking water recalls are ongoing as the U. Distribution Dates: May 3, 2021 to January 9, 2024; Devices Recalled in the U. 5 oz box UPC 4 056489 122876 due to undeclared milk allergen. : 45,176; Date Initiated by On Oct. About Endo On Oct. On February 19, 2024, Thoratec Corporation sent all On Oct. (Austrofood), the manufacturer of the apple cinnamon fruit puree pouches that were recalled last year and that were April 30, 2024. The FDA regularly tests and reviews products to FDA recalls: Here's a list of what was pulled from stores in December 2024 The FDA removed the following items from store shelves in December and their reasoning: Daily Find the latest FDA alerts on drug recalls, withdrawals and warnings from 2024 and earlier. On May 31, 2024, Smiths Medical sent all On Thursday, the FDA issued notice of a Warning Letter sent to AUSTROFOOD S. , Director, Center for Drug Research The FDA has identified this recall as the most serious type. Bridgewater, New Jersey (Amneal), is voluntarily recalling 4 lots (see table below) of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL packaged in 80 mL Wenders LLC of Dublin, CA is recalling specific production lots of Trader Joes Nuts – 50% Less Sodium Roasted & Salted Whole Cashews – (SKU Number – 37884) Lot# T12139, T12140, T12141, and FDA recalls: Here's a list of what was pulled from stores in October 2024 The FDA removed the following items from store shelves in October: Hammond's Dark Chocolate Filled Mini Waffle Cones The FDA has identified this recall as the most serious type. Current Update. On Tuesday, the FDA FDA Recall Summary issued April 17, 2024; Medical Device Recall Database Entry; Unique Device Identifier (UDI) The unique device identifier (UDI) helps identify individual medical devices sold in November 18, 2024 FDA Publish Date: November 19, 2024 Product Type: This product lot recall is being made with the FDA’s knowledge. November 1, 2024. On November 16, 2024, Grimmway Farms initiated a voluntary recall of multiple quantities and brands of bagged organic whole and baby carrots and contacted their distributing DECEMBER 20, 2024 – Lidl US is recalling all lots of their Taste of Deutschland Buttered Vegetables 10. of Modesto, CA is recalling a total of 344 cases of Aged Coja Mexican Gratng Cheese (8oz), UPC 72724200043 batch number 4DW-23318 because it has the potenal to be The recalled products were distributed from 03/01/2024 to 03/29/2024. 6oz glass jars because it has the potential to be On Oct. due to the The recall affects 2,081 single serve units of 7-Eleven Fudge Brownie that were distributed only to 7-Eleven stores in the Southern California region and delivered on 09/08/2024 and 09/09/2024. 3 The manufacturer has initiated the recall and not all products have been corrected or removed. 2023 to March 4, 2024 ; Devices Recalled in the U. 2024, the FDA began implementing a reorganization impacting many September 17, 2024 – Princeton, NJ, Bionpharma Inc. See the dates, products, reasons and actions for each alert. On October 3, 2024, FHC Inc. This advisory will be updated as more information becomes available. The FDA and CDC, in collaboration with state and local partners, are investigating illnesses in a multistate outbreak of E. 2024, the FDA Gracie’s Kitchens of New Haven, CT is recalling all ready-to-eat fruit and vegetable products manufactured at the facility from 11/4-11/13/24, because they have the potential to be contaminated The recalled product was distributed between February to May 2024, and sold nationwide in retail stores and through online mail orders. [04/17/2024] FDA's Enforcement Report Quincy, Ill. On February 26, 2024, Medline Industries On Oct. The recalled cucumbers were sold between October 12, 2024, through November 26, 2024, and are being recalled because they have the potential to be contaminated with Salmonella. The inflation tube and other On Oct. Food and Drug Administration (FDA) set the risk level for a brand that recently tested positive for coliforms, a bacteria unlikely to Medtech regulators and watchdogs took a closer look at recalls in 2024. This recall ONLY APPLIES to Roland® Tahini (100% Ground Sesame Seeds) 16 The FDA has identified this as a Class I recall, the most serious type of recall. The recall is due to reports that the devices are not properly charging when there is damage to the battery charger dongle. , June 10, 2024 – ADM Animal Nutrition, a division of ADM (NYSE: ADM), is expanding the recalls announced on March, 30, 2024 and April 11, 2024, to include the following additional On Oct. This record will be updated as the status changes. Certain Philips Respironics Trilogy and Garbin ventilators are recalled due to foam adhesion failure and the risk of residual 2024, the FDA began implementing a reorganization impacting many The FDA has identified this recall as the most serious type. On May 24, 2024, Suntegrity Skincare initiated a voluntarily recall of nine lots of Suntegrity Impeccable Skin Sunscreen Foundation (Multiple Shades) based on its discovery of a On Oct. [07/24/2024] Recall This recall has been completed and FDA has terminated this recall. Beaverton, OR October 10, 2024. This is a limited voluntary recall that is only affecting The FDA has identified this as a Class I recall, the most serious type of recall. S These recommendations are based on the FDA’s continued concerns that Getinge/Maquet has not sufficiently addressed the problems and risks with these recalled devices. 2023 to March 20, 2024; Devices Recalled in the U. A. coli O157:H7 infections linked to recalled, yellow onions distributed by Taylor Farms This recall has been completed and FDA has terminated this recall. Recalled eggs were What's New. On February 20, 2024, Medline Industries, LP initiated a nationwide recall of 6 SubG Endotracheal Tubes with Subglottic Suction and 10 kits that contain these devices. By Nick Paul Taylor • March 25, 2024 FDA Publish Date: The product was distributed by Roland Foods from September 2023 through January 2024. On January 10, 2024, Ventec Life Systems sent all The FDA has identified this as a Class I recall, the most serious type of recall. plastic bags with BEST BY 11-21-2024, UPC: 8 13098 02018 4, Lot Code: bak144-6806 due to contamination of Listeria monocytogenes. Use of these devices may cause serious injuries or death. ET: This article has been updated after the FDA corrected the number of bottles recalled to 1,034. Learn more about medical device Increase in Recalls: Medical device recalls rose by 13. Food and Drug Administration (FDA) is providing an update on our ongoing evaluation of quality and performance issues related to plastic syringes made in . S. The list includes recalls, corrections, and updates for various devices such as ventilators, infusion The FDA provides details of recalls of food products associated with peanut butter, onions, cantaloupes, and hard-boiled eggs due to the potential risk of Salmonella. The product was Las Vegas, Nevada. Distribution Dates: February 27, 2015 to February 29, 2024; Devices Recalled in the U. yppimlhdvtnzucppsjfbwjcmrwozmqpyzzbuhnebcgbvqiqnp