Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

26726–26750 of 39747

SevereFDA (Food)·F-3185-2015·2015-09-16
Jeni's Frozen Yogurt Recalled for Listeria Contamination Risk
Jeni's Splendid Ice Creams LLC is recalling specific lots of Tart, Lemon Buttermilk Frozen Yogurt due to potential Listeria monocytogenes contamination.
Product
Tart, Lemon Buttermilk Frozen Yogurt Bucket, 380, Jeni's Splendid Ice Creams, LLC, 3 gallons, plastic bucket, individually packed, frozen. Tart, Lemon Buttermilk Frozen Yogurt Pint Case, 280, Jeni's Splendid Ice Creams, LLC, pint size, plastic container, 8 pints per case…
Category
Food
Distribution
18 states
SevereFDA (Food)·F-3162-2015·2015-09-16
Jeni's Splendid Ice Creams Recalls Batdorf Black Coffee Products for Listeria Risk
Jeni's Splendid Ice Creams LLC is recalling Batdorf Black Coffee ice cream products in multiple states due to potential Listeria monocytogenes contamination.
Product
Batdorf Black Coffee Bucket, 366, Jeni's Splendid Ice Creams, LLC, 3 gallons, plastic bucket, individually packed, frozen. Batdorf Black Coffee Indie Case, Jeni's Splendid Ice Creams, LLC, 6oz, plastic container, 18 containers per case, frozen. Batdorf Black Coffee Indie…
Category
Food
Distribution
18 states
SevereNHTSA·15V574000·2015-09-15
Honda Recalls 2014-2015 Civic and Fit for Transmission Software Defect
Honda is recalling 2014-2015 Civic and 2015 Fit vehicles to update transmission software that may damage the drive pulley shaft, potentially causing loss of acceleration or wheel lockup.
Product
HONDA — HONDA FIT, CIVIC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V573000·2015-09-14
Nissan Recalls 2007-2012 Versa Vehicles Due to Front Coil Spring Fracture Risk
Nissan is recalling 2007-2012 Versa vehicles sold in 23 states and D.C. because road salt may corrode front coil springs, potentially causing them to fracture and puncture tires.
Product
NISSAN — NISSAN VERSA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V570000·2015-09-11
Triple E Unity Motorhomes Recalled for Battery Gas Leak Risk
Triple E is recalling 2015-2016 Unity motorhomes because the battery compartment was not properly sealed, allowing explosive gases to enter the vehicle and increasing fire risk.
Product
TRIPLE E — TRIPLE E UNITY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V568000·2015-09-10
Hyundai Recalls 2011-2012 Sonata Vehicles for Engine Crankshaft Defect
Hyundai is recalling 2011-2012 Sonata vehicles because metallic debris in the engine crankshaft may restrict oil flow, potentially causing engine failure and increasing crash risk.
Product
HYUNDAI — HYUNDAI SONATA
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·122-2015·2015-09-10
Pork Rind Factory Recalls Pork Rinds Due to Undeclared Allergens
The Pork Rind Factory is recalling approximately 18,406 pounds of pork rinds because they contain undeclared milk and soy allergens.
Product
The Pork Rind Factory — The Pork Rind Factory Recalls Pork Products Due To Misbranding and Undeclared Allergens
Category
Food
Distribution
4 states
SevereCPSC·15240·2015-09-10
Lota Recalls Glacier Bay and Schön Touchless Kitchen Faucets for Fire and Burn Hazards
Lota USA is recalling about 4,500 Glacier Bay and Schön touchless kitchen faucets sold at The Home Depot because the battery box can short circuit, overheat, or melt, posing fire and burn risks.
Product
Glacier Bay and Schön kitchen faucets
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-3059-2015·2015-09-09
Mahina Mele Farm Recalls Salted Macadamia Nuts Due to Salmonella
Mahina Mele Farm is recalling salted macadamia nuts after an FDA sample tested positive for Salmonella. Consumers should stop eating the product and return it to the store.
Product
Izzie Macs! Macadamia Nuts; Salted. Certified Organic Macadamia Nuts, 100% Big Island Grown. A Raw Food. sold in 6 oz. and 16 oz sizes. 6 oz, UPC 689076792677; 16 oz. UPC 689076792974 Mahina Mele Farm, Captain Cook, HI 96704
Category
Food
Distribution
10 states
CriticalFDA (Food)·F-3063-2015·2015-09-09
Mahina Mele Farm Recalls Chocolate Mac Nut Butter Due to Salmonella
Mahina Mele Farm is recalling Baby Bruddah's Chocolate Mac Nut Buttah because an ingredient sample tested positive for Salmonella.
Product
Baby Bruddah's Chocolate Mac Nut Buttah. 12 oz. container, UPC 735182242040 Mahina Mele Farm, Captain Cook, HI 96704
Category
Food
Distribution
10 states
CriticalFDA (Food)·F-3060-2015·2015-09-09
Mahina Mele Farm Recalls Macadamia Nuts Due to Salmonella Risk
Mahina Mele Farm is recalling Izzie Macs! Macadamia Nuts because an inspection sample tested positive for Salmonella. Consumers should stop eating the product and return it to the store.
Product
Izzie Macs! Macadamia Nuts; Unsalted. Certified Organic Macadamia Nuts, 100% Big Island Grown. A Raw Food. sold in 6 oz. and 16 oz sizes. 6 oz, UPC 689076793575; 16 oz. UPC 689076792776 Mahina Mele Farm, Captain Cook, HI 96704
Category
Food
Distribution
10 states
CriticalFDA (Food)·F-3062-2015·2015-09-09
Mahina Mele Farm Recalls Mac Nut Butter Due to Salmonella
Mahina Mele Farm is recalling Baby Bruddah's Mac Nut Buttah because an ingredient sample tested positive for Salmonella.
Product
Baby Bruddah's Mac Nut Buttah. 12 oz. container, UPC 753182242019 Mahina Mele Farm, Captain Cook, HI 96704
Category
Food
Distribution
10 states
CriticalFDA (Food)·F-3061-2015·2015-09-09
Mahina Mele Farm Recalls Macadamia Nuts Due to Salmonella
Mahina Mele Farm is recalling Izzie Macs! Macadamia Nuts because an inspection sample tested positive for Salmonella.
Product
Izzie Macs! Macadamia Nuts; salted and unsalted pieces. Certified Organic Macadamia Nuts, 100% Big Island Grown. A Raw Food. sold in 5 lb. bag; Mahina Mele Farm, Captain Cook, HI 96704
Category
Food
Distribution
10 states
CriticalFDA (Food)·F-3076-2015·2015-09-09
Good Seed Recalls Mung Bean Sprouts Due to Listeria Risk
Good Seed, Inc. is voluntarily recalling mung bean sprouts due to potential Listeria monocytogenes contamination. The products were distributed to retail stores in Virginia, Maryland, and New Jersey.
Product
Mung Bean sprouts, 1, 2 & 10-lb clear plastic bags labeled GOODSEED Mung Bean Sprouts, Keep Refrigerated
Category
Food
Distribution
3 states
SevereFDA (Drugs)·D-1414-2015·2015-09-09
Bi-Est Cream Recalled for Potential Penicillin Cross Contamination
South Coast Specialty Compounding is recalling Bi-Est cream due to potential penicillin cross contamination. The recall covers 36 prescriptions distributed nationwide.
Product
Bi-Est (estriol,estradiol), Progesterone, Testosterone cream, Rx only, Manufactured by Park Compounding, Irvine, CA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2560-2015·2015-09-09
Customed Arthroscopy Packs Recalled for Sterilization Validation Issues
Customed, Inc. is recalling 45 Arthroscopy Packs distributed in Puerto Rico due to inadequate validation of sterilization processes and package integrity.
Product
ARTHROSCOPY PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
Category
Medical Device
Distribution
1 state
SevereFDA (Devices)·Z-2558-2015·2015-09-09
Customed Cysto TUR Pack Recalled for Sterilization Validation Issues
Customed, Inc. is recalling 290 packs of Cysto TUR Pack due to inadequate validation of sterilization processes and package integrity.
Product
CYSTO TUR PACK CUSTOMED 10/CS REV. C 10/13 NON STERILE Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
Category
Medical Device
Distribution
1 state
SevereFDA (Devices)·Z-2676-2015·2015-09-09
Customed Gauze Sponges Recalled for Sterilization Process Validation Issues
Customed, Inc. is recalling 19,328 units of 4"x4" 16-ply gauze sponges distributed in Puerto Rico due to inadequate validation of sterilization processes and package integrity.
Product
GAUZE SPONGE 4"X4" 16 PLY SOFT 1280/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
Category
Medical Device
Distribution
1 state
SevereFDA (Drugs)·D-1338-2015·2015-09-09
Leucovorin Calcium Capsules Recalled for Potential Penicillin Contamination
South Coast Specialty Compounding is recalling Leucovorin Calcium capsules due to potential penicillin cross-contamination. The affected products were distributed nationwide.
Product
Leucovorin Calcium capsules, 10 mg, Rx only, Manufactured by Park Compounding, Irvine, CA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2697-2015·2015-09-09
Customed O.B. Pack Hospital 3/CS Recalled for Sterilization Validation Issues
Customed, Inc. is recalling 147 units of O.B. Pack Hospital 3/CS in Puerto Rico due to inadequate validation of sterilization processes and package integrity.
Product
O.B. PACK HOSPITAL 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
Category
Medical Device
Distribution
1 state
SevereFDA (Devices)·Z-2545-2015·2015-09-09
MediTrace Cadence Defibrillation Electrodes Recalled for Wire Insulation Damage
Covidien LLC is recalling MediTrace Cadence Adult Multi-Function Defibrillation Electrodes due to potential wire insulation damage that may cause burns or reduced therapy.
Product
MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2707-2015·2015-09-09
Customed Cesarean PK 4/CS Recalled for Sterilization Validation Defects
Customed, Inc. is recalling 48 units of CESAREAN PK 4/CS surgical kits due to inadequate validation of sterilization processes and package integrity.
Product
CESAREAN PK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
Category
Medical Device
Distribution
1 state
SevereFDA (Devices)·Z-2527-2015·2015-09-09
Recall of Mahurkar Acute Dual Lumen Catheter Trays Due to Sterility Concerns
Covidien LLC is recalling 8 kits of Mahurkar Acute Dual Lumen Catheter Trays because sterility may be compromised.
Product
Mahurkar Acute Dual Lumen Catheter Tray, High Flow¿ Pre-Curved with IC* Safety Components, 13.5 FR x 13.5 cm Item Code: 8888135139 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2546-2015·2015-09-09
MediTrace Cadence Defibrillation Electrodes Recalled for Wire Insulation Damage
Covidien LLC is recalling MediTrace Cadence Adult Zoll defibrillation electrodes due to potential wire insulation damage that could cause burns or reduced therapy.
Product
MediTrace Cadence Adult Zoll, Preconnect Defibrillation Electrode, Nonsterile Item Code:22770PC
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2655-2015·2015-09-09
Customed Suction Catheter Kits Recalled for Sterilization Validation Issues
Customed, Inc. is recalling 8,300 suction catheter kits distributed in Puerto Rico due to inadequate validation of sterilization processes and package integrity.
Product
SUCTION CATHETER KIT CUSTOMED 50/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
Category
Medical Device
Distribution
1 state

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