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.

4826–4850 of 7439

CriticalFDA (Food)·F-2269-2015·2015-05-20
Aurora Recalls Roasted Salt Mixed Nuts Due to Salmonella Risk
Aurora Products, Inc. is voluntarily recalling various sizes of Roasted Salt Mixed Nuts because they may be contaminated with Salmonella.
Product
Roasted Salt Mixed Nuts: Aurora, 4.5 oz. Plastic Pouch, UPC: 65585200252; Aurora, 20 oz. Plastic Tub, UPC: 65585200340; Aurora, 10 oz. Plastic Pouch, UPC: 65585200804, Aurora, Bulk, No UPC, Belmont Market, 20 oz. Plastic Tub, UPC: 65585200340, Food Emporium Brand Products, 6.5 oz
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2259-2015·2015-05-20
Aurora Nut Tray Assortment Recalled for Salmonella Risk
Aurora Products is recalling 4 Section Nut Tray Assortments due to potential Salmonella contamination. The recall covers specific UPCs and best-by dates in the US, Canada, and Bermuda.
Product
4 Section Nut Tray Assortment: Aurora 13 oz. Plastic Tray UPC: 65585200141; Food Emporium Brand Products 13 oz. Plastic Tray UPC: 1119079011
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2266-2015·2015-05-20
Aurora Recalls San Fernando Sunshine Mix Due to Salmonella Risk
Aurora Products, Inc. is recalling 84 pounds of San Fernando Sunshine Mix due to a potential Salmonella hazard. The product was distributed in the US, Canada, and Bermuda.
Product
San Fernando Sunshine Mix: Gourmet Garage, 11 oz. Plastic Cup, UPC: 79084505936
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2263-2015·2015-05-20
Aurora Forest Bounty Grail Mix Recalled for Salmonella Risk
Aurora Products is recalling Forest Bounty Grail Mix due to a potential Salmonella contamination risk. The recall covers specific 13 oz and 17.5 oz packages distributed in the US, Canada, and Bermuda.
Product
Forest Bounty Grail Mix: Aurora, 13 oz. Plastic Cup, UPC: 65585200571; Aurora, 13 oz. Plastic Pouch, UPC: 65585200290; Aurora, 17.5 oz. Plastic Cup, UPC: 65585200496
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2264-2015·2015-05-20
Aurora Products Recalls Raisin Nut Party Mix Due to Salmonella Risk
Aurora Products, Inc. is recalling Raisin Nut Party Mix products due to a potential Salmonella contamination. The recall covers specific brands and sizes distributed in the US, Canada, and Bermuda.
Product
Raisin Nut Party Mix: Aurora, 11.0 oz. Plastic Cup, UPC: 65585200094; Ernest Klein, 11.0 oz. Plastic Cup, UPC: 65585200094, Food Emporium Brand Products, 7.5 oz. Gift Bag, UPC: 1119079050; Gauls Market Brand Products, 11.0 oz. Plastic Cup, UPC: 65585200094; Harvest Co Op Market,
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2265-2015·2015-05-20
Aurora Products Recalls Roasted Mixed Nuts Due to Salmonella Risk
Aurora Products, Inc. is voluntarily recalling specific lots of Roasted Mixed Nuts No Salt because they may be contaminated with Salmonella.
Product
Roasted Mixed Nuts No Salt: Gourmet Garage, 9 oz. Plastic Cup, UPC: 79084506010; Hannaford, 9.0 oz. Plastic Cup, UPC: 72543994507
Category
Food
Distribution
Distributed nationwide
CriticalNHTSA·15E040000·2015-05-18
Takata Frontal Driver Air Bag Inflator Module Recall
Takata is recalling specific frontal driver air bag inflator modules that may rupture during deployment, potentially causing serious injury or death.
Product
AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·15E043000·2015-05-18
Takata Frontal Passenger Air Bag Inflator Recall for Honda and Mazda Vehicles
Takata is recalling specific frontal passenger air bag inflators for certain Honda and Mazda vehicles due to a risk of rupture during deployment.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0982-2015·2015-05-13
Physician Preferred Medical Recalls Epel 18 mg Estradiol Pellets Due to Sterility Failure
Physician Preferred Medical, LLC is recalling Epel 18 mg Estradiol Pellets because the specific lot failed sterility testing. The product was distributed in Arizona and Kansas.
Product
Epel 18 mg Estradiol Pellet, For In Office Use Only, For In Office Administration Only, Not for Resale or Dispensing to an Individual Patient, Rx Only, Preferred Physician Medical LLC, 405-551-8216
Category
Drug
Distribution
2 states
CriticalFDA (Drugs)·D-0986-2015·2015-05-13
FDA Recalls Unapproved Anabolic Steroid Product HALO-70 MEGA MASS BUILDER
The FDA is recalling HALO-70 MEGA MASS BUILDER capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.
Product
HALO-70 MEGA MASS BUILDER (4-chloro-17a-methyl-androst-1,4-diene-3b,17b-diol 35mg), Capsules, 60 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0991-2015·2015-05-13
Ultra ZX Dietary Supplement Recalled for Undeclared Sibutramine and Phenolphthalein
Ultra ZX Labs is recalling Ultra ZX dietary supplements because FDA testing found undeclared sibutramine and phenolphthalein. The product was marketed without an approved NDA or ANDA.
Product
ULTRA ZX DIETARY SUPPLEMENT (Extracto de Naranjo Amargo 70, Extracto de semilla de Sen 47.6, Lagrima de Coix 42, Almidon Medico 84), 30 capsule bottles, Manufactured and distributed by: Ultra ZX Labs, L.L.C. 2525 SW 3rd Ave Apt 1704 Miami, Florida 33129-2068.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0988-2015·2015-05-13
FDA Recalls Estrastain Pro-Anabolic Mass and Hardening Complex Capsules
Anabolic Science Labs LLC is recalling Estrastain Pro-Anabolic Mass and Hardening Complex capsules because they contain unapproved synthetic hormone ingredients.
Product
ESTRASTAIN PRO-ANABOLIC MASS AND HARDENING COMPLEX (Estra-4,9,11-triene-3,17-dione 15mg, 2a-3a-epithio-17a-methyl-5a-androstan-17b-ol 10 mg), Capsules, 60 count bottle, Manufactured for: Wyked Labs LLC, Winter Park, FL 32789
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2196-2015·2015-05-13
La Terra Fina Spinach Artichoke Dip Recalled for Listeria Risk
La Terra Fina is recalling specific lots of Chunky Spinach Artichoke & Parmesan Dip because the chopped spinach ingredient tested positive for Listeria monocytogenes.
Product
La Terra Fina Chunky Spinach Artichoke & Parmesan Dip 31-ounce tub Keep refrigerated 31-ounce tub; UPC: 6-40410-51193-4 Item number 407600 - Costco Item number 4300193 - Smart and Final 10 oz. Retail size - UPC 6-40410-51327-3 Manufactured by La Terra Fina, Union City
Category
Food
Distribution
6 states
CriticalFDA (Drugs)·D-0994-2015·2015-05-13
Forever Beautiful Bee Pollen Recalled for Contaminants
REFA Enterprises is recalling Forever Beautiful Bee Pollen capsules because FDA analysis found the product contains sibutramine and phenolphthalein.
Product
Forever Beautiful BEE POLLEN, capsules, 250mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2194-2015·2015-05-13
La Terra Fina Spinach Dip Recalled for Listeria Contamination
La Terra Fina is recalling Organic Thick & Creamy Spinach Dip and Spread because the chopped spinach ingredient tested positive for Listeria monocytogenes.
Product
La Terra Fina Organic Thick & Creamy Spinach Dip and Spread; Made with Greek Yogurt. 24 oz. plastic tub (1 lb. 8 oz,) 680 g: Keep refrigerated UPC 640410513730. Manufactured by" La Terra Fina, Union City, CA 94587
Category
Food
Distribution
6 states
CriticalFDA (Drugs)·D-0993-2015·2015-05-13
REFA Enterprises Recalls Forever Beautiful INFINITY Capsules for Unapproved Ingredients
REFA Enterprises is recalling Forever Beautiful INFINITY capsules because FDA analysis found the product contains sibutramine and phenolphthalein without an approved NDA/ANDA.
Product
Forever Beautiful INFINITY, capsules, 300mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0977-2015·2015-05-13
FDA Recalls EDGE Weight Release Capsules Containing Unapproved Drugs
Detox Transforms is recalling EDGE Amplified Weight Release capsules because the product contains undeclared phenolphthalein and fluoxetine, making it an unapproved drug.
Product
EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00417 4.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0979-2015·2015-05-13
AMPD GOLD Bee Pollen Recalled for Undeclared Sildenafil
Detox Transforms is recalling AMPD GOLD Bee Pollen capsules because they contain undeclared sildenafil, making them unapproved drugs.
Product
AMPD GOLD Bee Pollen capsules, 350 mg, 60-count bottle, Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00418 1.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0981-2015·2015-05-13
FDA Recalls iNSANE Bee Pollen Capsules Containing Unapproved Drugs
The FDA is recalling iNSANE Bee Pollen capsules because they contain undeclared phenolphthalein and fluoxetine, making them unapproved drugs.
Product
iNSANE Bee Pollen capsules, 200 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00408 2.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2153-2015·2015-05-13
Spiceco Recalls Hungarian Paprika Due to Undeclared Peanut Protein
Spiceco is recalling Pride of Szeged Sweet Hungarian Paprika because it may contain undeclared peanut protein. The recall includes additional products containing the implicated paprika.
Product
Pride of Szeged Hungarian Exquisite 100 % Sweet Delicacy Paprika, Net Wt. 5 oz., 142g, UPC 0 78006 00010 2
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0989-2015·2015-05-13
FDA Recalls Unapproved Anabolic Steroid Supplements from Anabolic Science Labs
Anabolic Science Labs is recalling SWOLL-250 Super Mass Builder Quad Stack capsules because they contain unapproved synthetic hormone ingredients.
Product
SWOLL-250 SUPER MASS BUILDER QUAD STACK (18-Methylestr-4-en-3-one-17b-ol 15mg, 6-a-Chloro-androst-4-en-17b-ol-3-one 15mg, 13-ethyl-3-methoxy-gona-2,5(10)-diene-17-one 15mg, 2,17a-dimethyl-5a-androsta-1-en-17b-ol-3-one 3 mg), Capsules, 90 count bottle, Manufactured for: Wyked Labs
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0978-2015·2015-05-13
Detox Transforms Recalls iNDiGO Capsules Containing Undeclared Phenolphthalein
Detox Transforms is recalling iNDiGO capsules because they contain undeclared phenolphthalein, making the product an unapproved drug.
Product
iNDiGO capsules, 220 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00404 4.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2141-2015·2015-05-06
Red River Foods Recalls Macadamia Nuts Due to Salmonella Risk
Red River Foods is voluntarily recalling 13,750 lbs of South Africa Macadamia Nuts after a repacker in Texas tested positive for Salmonella.
Product
Style 2 South Africa Macadamia Nuts,
Category
Food
Distribution
5 states
CriticalFDA (Food)·F-2115-2015·2015-05-06
JCB Flavors Recalls Chili Powder Due to Peanut Allergen Contamination
JCB Flavors is recalling specific lots of chili powder and seasonings because the ground cumin ingredient tested positive for trace peanut allergens.
Product
JCB FLAVORS, LLC, Product Code 8102920812, 8102923212, 8102921606, Chili Powder #810292 , 12 x 8oz jar, UPC: 66049244520, 66049244506.
Category
Food
Distribution
7 states
CriticalFDA (Food)·F-2139-2015·2015-05-06
JCB Flavors Recalls Seasonings Containing Peanut Allergen
JCB Flavors is recalling specific seasonings that used ground cumin containing trace peanut allergens. The recall affects products distributed to several states.
Product
JCB FLAVORS, LLC, Product Code 10044001, 10044002, 10044009, 1004425, Chili Powder #100440, "1 x 5lb jug, 4 x 5 lb jugs, 4x5lb bags, 25 lb bulk, 10 lb bulk, 12 x 8 oz". UPC 014641000183, 014641000176.
Category
Food
Distribution
7 states