Severity 5 of 5

Critical recalls

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

What “critical” means here

Severity 5 (Critical) covers recalls where deaths or serious injuries have been reported, or where the agency itself classified the action as the highest severity (FDA Class I, NHTSA 'death/serious injury reported'). These are the recalls you should treat as urgent — stop using the product immediately and follow the agency's guidance. Common Severity-5 categories are pathogen-contaminated ready-to-eat foods (Listeria, E. coli O157, Salmonella), drug products with confirmed adverse-event reports, and vehicle defects with documented fatal crashes.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

701–725 of 7436

CriticalFDA (Food)·F-1671-2024·2024-08-14
Palmer Candy and Meijer Popcorn Products Recalled for Salmonella
Palmer & Company is recalling Palmer Candy Drizzled Caramel Corn and Meijer Drizzled Caramel Popcorn Snack Bowls due to potential Salmonella contamination. Products were distributed nationwide in the United States and Canada.
Product
1. Palmer Candy Drizzled Caramel Corn, Item 19271, Net Wt. 16/5oz tubs, UPC 77343 19271 2. Meijer Drizzled Caramel Popcorn Snack Bowl, Net Wt. 12oz, UPC 60236 18830, 8/12oz case
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1535-2024·2024-08-07
Diamond Shruumz Gummies Recalled for Toxic Levels of Muscimol
Diamond Shruumz Gummies (Micro Dose Sour Peach Apple) manufactured by Prophet Premium Blends, LLC, are being recalled by the FDA due to toxic levels of muscimol. The Class I recall affects approximately 248,007 products distributed nationwide.
Product
Diamond Shruumz Gummies - Micro Dose Sour Peach Apple UPC 755003861386
Category
Food
Distribution
51 states
CriticalFDA (Food)·F-1540-2024·2024-08-07
Diamond Shruumz Gummies recalled for toxic muscimol levels
Diamond Shruumz Gummies Mega/Extreme Dose Peach Paradise contain toxic levels of muscimol. The FDA is recalling all 248,007 units distributed nationwide.
Product
Diamond Shruumz Gummies - Mega/Extreme Dose Peach Paradise UPC 810133320384
Category
Food
Distribution
51 states
CriticalFDA (Drugs)·D-0620-2024·2024-08-07
Dietary Supplement Recalled for Undeclared Diclofenac and Omeprazole
SoloVital's Umary Hyaluronic Acid supplement was recalled because FDA testing found it contains undeclared Diclofenac and Omeprazole. The product, marketed without approved NDA/ANDA, affected 1,331 bottles distributed nationwide.
Product
Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.
Category
Drug
Distribution
Distributed nationwide
CriticalUSDA FSIS·023-2024-EXP·2024-07-30
Boar's Head Expands Recall of Deli Meats Due to Listeria
Boar's Head is recalling 7 million pounds of ready-to-eat meat and poultry products due to possible Listeria contamination linked to a multistate outbreak.
Product
Boar's Head Provisions Co., Inc. — Boar's Head Provisions Co. Expands Recall for Ready-To-Eat Meat and Poultry Products Due to Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide
CriticalUSDA FSIS·023-2024·2024-07-26
Boar's Head Recalls Deli Meats Due to Listeria Contamination
Boar's Head Provisions is recalling liverwurst and other deli meats nationwide due to possible Listeria monocytogenes contamination linked to a multistate outbreak.
Product
Boar's Head Provisions Co., Inc. — Boar's Head Provisions Co. Recalls Ready-To-Eat Liverwurst And Other Deli Meat Products Due to Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2319-2024·2024-07-24
Abiomed Impella CP with SmartAssist heart pump units recalled for failed inspection
Abiomed is recalling 9 Impella CP with SmartAssist heart pump units that failed inspection and were inadvertently released. The devices were distributed in Florida, Massachusetts, Ohio, and Texas.
Product
Impella CP with SmartAssist, Product No.: 1000080 (REF 0048-0003). left heart support blood pump
Category
Medical Device
Distribution
4 states
CriticalFDA (Food)·F-1483-2024·2024-07-24
Deluxe Roasted Salted Mixed Nuts recalled for undeclared peanut allergen
DSD Merchandisers recalls Deluxe Roasted Salted Mixed Nuts (Item 99651) for undeclared peanut allergen, with distribution in six western states and a sell-by date of October 9, 2024. Consumers with peanut allergies should not consume this product.
Product
Deluxe Roasted Salted Mixed Nuts ITEM NUMBER 99651 UPC: 6-51433-99651-6 SELL BY: 10/09/2024
Category
Food
Distribution
6 states
CriticalFDA (Food)·F-1464-2024·2024-07-17
Crecelac Infant Powdered Formula Recalled Due to Cronobacter
Dairy Manufacturers' Crecelac Infant formula (5,376 cans distributed in Texas) is recalled due to Cronobacter spp. detected during FDA testing. Products lack required premarket evaluation for food safety and nutritional standards.
Product
Crecelac Infant 0-12 powdered infant formula with iron 12.4 oz cans
Category
Food
Distribution
1 state
CriticalFDA (Devices)·Z-2252-2024·2024-07-17
Medical Device Recall: Bausch+Lomb Intravitreal Injection Kit Unvalidated Sterilization
Synergetics Inc is recalling Bausch+Lomb I-PACK Intravitreal Injection Kits because sterilization certificates could not be validated by the supplier. The FDA classified this as Class I.
Product
BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)
Category
Medical Device
Distribution
Distributed nationwide
CriticalUSDA FSIS·021-2024·2024-07-13
Taylor's Sausage Recalls Landjaeger Products for Undeclared Soy Allergen
Taylor's Sausage is recalling approximately 74 pounds of ready-to-eat Landjaeger sausage due to misbranding and undeclared soy. The product was distributed in California and Oregon.
Product
Taylor's Sausage, Inc. — Taylor's Sausage, Inc. Recalls Ready-To-Eat Landjaeger Sausage Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
2 states
CriticalFDA (Devices)·Z-2140-2024·2024-07-03
Life2000 Ventilator systems recalled due to battery charging failure risk
The Life2000 Ventilator may fail to charge or experience intermittent charging behavior due to damage to the battery charger dongle. This FDA Class I recall affects approximately 2,510 units distributed nationwide.
Product
Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and BT-20-0002AP. The Life2000 ventilation system includes the Life2000 ventilator which has its individual label.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1424-2024·2024-07-03
Pop a Nosh Mixed Munch snacks recalled for undeclared wheat
AMB FOODS INC is recalling Pop a Nosh Mixed Munch snacks due to undeclared wheat allergen. Approximately 2,100 units distributed in New York contain wheat, which is not labeled on the product.
Product
Pop a Nosh Mixed Munch; Regular Flavor; 8oz plastic bag; Potato Chips, Popcorn, Pretzels; UPC 914669941
Category
Food
Distribution
1 state
CriticalCPSC·24744·2024-06-27
Dania Furniture Recalls Hayden Bookcase Due to Tip-Over Hazard
Dania Furniture is recalling about 940 Hayden Bookcases sold from November 2017 through February 2024 because the bookcase can tip over and cause entrapment injuries if not anchored to the wall. A 4-year-old child died from a tip-over incident in August 2023.
Product
Hayden Bookcase
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1388-2024·2024-06-26
New Seasons Market Strawberry Rhubarb Bakewell Tart Recalled for Undeclared Almond
New Seasons Market is recalling its Strawberry Rhubarb Bakewell Tart due to undeclared almond. The 261 units distributed in Oregon and Washington pose an allergen risk to consumers with almond allergies.
Product
New Seasons Market Strawberry Rhubarb Bakewell Tart, packaged in a plastic clamshell with scale label. Contains Milk, Wheat, Eggs.
Category
Food
Distribution
2 states
CriticalFDA (Food)·F-1370-2024·2024-06-19
Cultured Dairy Product Recalled for Possible Salmonella Contamination
Grande Grande Primo Y45 cultured dairy product is being recalled due to possible Salmonella contamination. The product was distributed across multiple U.S. states and internationally to Canada, Ecuador, and Japan.
Product
Grande Grande Primo Y45 Cultured Dairy Product. Product Code: 32400. Grade A. Pasteurized. Net Wt 50 lbs. Ingredients: Whey Protein Concentrate, Skim Milk, Yogurt Cultures (L. bulgaricus, S. thermophilus). Heat Treated After Culturing. Contains Milk. Grande Custom Ingr
Category
Food
Distribution
24 states
CriticalFDA (Food)·F-1352-2024·2024-06-19
Newly Weds Foods Breader Recalled for Potential Salmonella Contamination
Newly Weds Foods is recalling its Breader X7 in 50-pound bags due to potential Salmonella contamination in an ingredient. The contamination poses a serious health risk.
Product
Newly Weds Foods, LLC A51638 Breader X7 50lb bag
Category
Food
Distribution
3 states
CriticalFDA (Food)·F-1366-2024·2024-06-19
Grande Bravo 600 Whey Protein Recalled for Possible Salmonella Contamination
Grande Cheese Company is recalling Grande Bravo 600 Functional Whey Protein for possible Salmonella contamination. The affected product was distributed to 24 US states and to Canada, Ecuador, and Japan.
Product
Grande Bravo 600 Functional Whey Protein SKU 32106. 34% Protein. Grade A. Pasteurized. Net Wt 50 lbs. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
CriticalFDA (Food)·F-1345-2024·2024-06-19
Baraka Brand Ground Black Pepper Recalled for Potential Salmonella Contamination
U.B.C. Food Distributors is recalling Baraka brand ground black pepper due to potential Salmonella contamination. The product is packaged in 7oz retail containers with UPC 8 22514 26626 6.
Product
Baraka brand ground black pepper packaged in 7oz retail containers with UPC 8 22514 26626 6; 10 units per case
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0554-2024·2024-06-19
Docetaxel Injection Recalled Nationwide for Stopper Particulate Matter
Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper contaminating the drug. The recall affects 2,806 vials distributed nationwide.
Product
DOCETAXEL — DOCETAXEL (DOCETAXEL ANHYDROUS)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1353-2024·2024-06-19
Frozen Scallop Ingredient Recalled Due to Potential Salmonella Contamination
Kerry, Inc is recalling Scallop Pot Seas frozen scallop ingredient due to potential Salmonella contamination. The product was distributed to commercial customers in multiple U.S. states and Canada.
Product
Scallop Pot Seas 703161, 860 kg. SAP Code: 30589206. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
Category
Food
Distribution
8 states
CriticalCPSC·24265·2024-06-13
Magnetic Chess Games Recalled for High-Powered Magnet Ingestion Hazard
About 2,600 magnetic chess games with 20 magnet pieces sold on Temu.com from December 2023 through February 2024 are recalled because the magnets violate federal toy magnet regulations and pose a serious ingestion hazard.
Product
1 Set Puzzle "Magnetic", "Magnetism", or "Magnetism Intelligence Strategy Game" Magnetic Battle Chess Games
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1328-2024·2024-06-12
Danisco USA Inc. recalls GS 1134 Kreme WIP for potential Salmonella
Danisco USA Inc. is recalling GS 1134 Kreme WIP, a food ingredient product, due to potential Salmonella contamination affecting multiple U.S. states, Canada, and Mexico.
Product
GS 1134 Kreme WIP, 25 kg / 55.12 lb bag
Category
Food
Distribution
24 states
CriticalFDA (Food)·F-1339-2024·2024-06-12
Food Preservative Recalled for Potential Salmonella Contamination
Danisco USA Inc. is recalling Germantown Gard (A) Preservative due to potential Salmonella contamination. The recall affects 21,000 kg distributed across the US, Canada, and Mexico.
Product
Germantown Gard (A) Preservative, 25 kg / 55.12 lb bag
Category
Food
Distribution
24 states
CriticalFDA (Food)·F-1309-2024·2024-06-12
Food Stabilizer and Emulsifier System Recalled for Potential Salmonella
Danisco USA Inc. is recalling Grindsted Hi-Dress CDS 1880 Stabilizer and Emulsifier System due to potential Salmonella contamination. The product was distributed to facilities across multiple US states, Canada, and Mexico.
Product
Grindsted Hi-Dress CDS 1880 Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
Category
Food
Distribution
24 states