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

24926–24950 of 39703

SevereFDA (Devices)·Z-0981-2016·2016-03-02
Xeridiem EndoVive 3s Low Profile Balloon Kits Recalled for Valve Leakage
Xeridiem Mediem Medical Devices Inc is recalling 39 EndoVive 3s Low Profile Balloon Kits because the feeding valve may close inconsistently, allowing fluid to leak.
Product
EndoVive 3s Low Profile Balloon Kits Part Number: M00548320 (XMD P/N 70-0050-B12) The EndoVive 3s Low Profile Balloon is intended to provide gastric access through a gastrointestinal stoma tract for enteral feeding, medication administration and gastric decompression. The…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0629-2016·2016-03-02
Mahina Mele Farm Recalls Izzie Macs! Macadamia Nuts Due to Salmonella Risk
Mahina Mele Farm is recalling Izzie Macs! Macadamia Nuts because samples 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. plastic bag and 16 oz. plastic bag. UPC - 6 oz.: 689076793575; UPC 16 oz.: 689076792776. Mahina Mele Farm 87-2642 Mamalahoa Hwy. Captain Cook, HI…
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-0801-2016·2016-03-02
Cook Inc. Recalls Femoral Artery Pressure Monitoring Catheters Due to Tip Fracture Risk
Cook Inc. is recalling specific femoral artery pressure monitoring catheter sets and trays because a manufacturing defect may cause the catheter tip to fracture or separate.
Product
Femoral Artery Pressure Monitoring Catheter Sets and Trays The subject sets and trays are comprised of a single-lumen uncoated or heparin-coated catheter. Product catalog numbers with heparin coating are designated by the suffix BH.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0930-2016·2016-03-02
Xeridiem EndoVive 3s Balloon Kits Recalled for Feeding Valve Leakage
Xeridiem is recalling 34 EndoVive 3s Low Profile Balloon Kits because the feeding valve may leak gastric contents when disconnected.
Product
EndoVive 3s Low Profile Balloon Kits Part Number: M00548840 (XMD P/N 70-0050-320) The EndoVive 3s Low Profile Balloon is intended to provide gastric access through a gastrointestinal stoma tract for enteral feeding, medication administration and gastric decompression. The…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V126000·2016-03-02
Forest River Recalls 2016-2017 Coachman and Dynamax Recreational Vehicles
Forest River is recalling 176 recreational vehicles due to an ignition switch defect that may cause stalling or loss of safety systems.
Product
COACHMEN — COACHMEN, DYNAMAX ORION, REV
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0804-2016·2016-03-02
Maquet Flow-i Anesthesia System Recalled for Electrical Control Issues
Maquet is recalling seven Flow-i Anesthesia Systems in the US due to electrical issues in control and monitoring sub-systems that can cause restarts or system disabling.
Product
Flow-i Anesthesia System Product Usage: The indication for the Flow-i Anesthesia System is administering inhalation anesthesia while controlling the entire ventilation of patients with no ability to breath, as well as in supporting patients with a limited ability to breath.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0866-2016·2016-03-02
GSI Group Recalls PRN 50-M+ Paper Chart Recorders for Fire Risk
GSI Group Inc. is recalling 2,257 PRN 50-M+ Paper Chart Recorders due to a risk of fire or electrical shock.
Product
PRN 50-M+, GE part number 2062759-001, manufacturer part number 600-23310-01 Product Usage: The PRN 50M+ Paper Chart Recorder thermally records patient data on a paper strip. This device is intended for use under direct supervision of a licensed health care practitioner.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0631-2016·2016-03-02
Mahina Mele Farm Recalls Raw Mac Nut Butter Due to Salmonella
Mahina Mele Farm is recalling Baby Bruddah's Mac Nut Buttah because samples of raw macadamia nuts tested positive for Salmonella.
Product
Baby Bruddah's Mac Nut Buttah; Certified Organic by International Certification Services Inc.. From the Big Island, A raw food. Sold in 12 oz. plastic tub. UPC number: 753182242019 Mahina Mele Farm 87-2642 Mamalahoa Hwy. Captain Cook, HI 96704
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0726-2016·2016-03-02
Keystone Recalls Medicated Better Braids Spray Due to Staphylococcus aureus
Keystone Laboratories is recalling Medicated Better Braids, La Laque (salicylic acid) Spray due to a positive Staphylococcus aureus test result.
Product
Medicated Better Braids, La Laque (salicylic acid) Spray, 2%,12 Fl. OZ. (355 ml.) bottle, Distributed by Keystone Laboratories, Memphis, TN 38101-2026, UPC 0 70596 00422 5.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0623-2016·2016-03-02
Purple Cow Cookie Butter Ice Cream Recalled for Mislabeling
House of Flavors is recalling Purple Cow Limited Edition Cookie Butter Ice Cream because the cups contain Butter Pecan ice cream instead.
Product
Purple Cow Limited Edition Cookie Butter Ice Cream, 8 oz. cups, packed in paper cartons
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0624-2016·2016-03-02
CSFPDX Recalls Wild Albacore Tuna Cans Due to Under-Processing Concerns
CSFPDX, LLC is voluntarily recalling 142 cans of Wild Albacore Tuna because they may be under-processed, posing a risk of Clostridium botulinum contamination.
Product
Labeled "CSFISHERY COMMUNITY SUPPORTED FISHERY Wild Albacore Tuna, 64 oz.., Ingredients: Oregon Albacore Tuna, Sea Salt" Label is black ink on an off white label. No UPC
Category
Food
Distribution
1 state
SevereNHTSA·16V128000·2016-03-02
Toyota and Lexus Recall Vehicles for Air Bag Inflator Rupture Risk
Toyota is recalling specific 2008-2010 Lexus SC, Corolla, Corolla Matrix, and Pontiac Vibe vehicles because the passenger air bag inflator may rupture during deployment.
Product
LEXUS — LEXUS, TOYOTA, PONTIAC SC, COROLLA MATRIX, COROLLA, VIBE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V122000·2016-03-01
Maserati Recalls Ghibli and Quattroporte Due to Floor Mat Defect
Maserati is recalling 2014-2016 Ghibli and Quattroporte vehicles because the driver-side floor mat anchor may break, allowing the mat to trap the accelerator pedal.
Product
MASERATI — MASERATI GHIBLI, QUATTROPORTE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V120000·2016-02-29
Jayco Eagle Trailers Recalled for Unprotected Solar Battery Cable Fire Risk
Jayco is recalling 2016 Eagle fifth wheels and travel trailers because an unprotected solar battery cable may short circuit and cause a fire.
Product
JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER, JAYCO FIFTH WHEEL EAGLE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V113000·2016-02-26
Chrysler Recalls 2015-2016 Dodge Dart Vehicles for Software Defect
Chrysler is recalling certain 2015 and 2016 Dodge Dart vehicles because a missing software backup in the powertrain control module may increase the risk of a crash.
Product
DODGE — DODGE DART
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·021-2016·2016-02-25
Sally Sherman Foods Recalls Chicken Salad Products Due to Listeria Risk
Sally Sherman Foods is recalling approximately 3,004 pounds of chicken salad products due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Product
U.F.S. Industries, Inc. — Sally Sherman Foods Firm Recalls Chicken Salad Products Due to Possible Listeria Contamination
Category
Food
Distribution
5 states
SevereNHTSA·16V109000·2016-02-25
Honda Recalls 2014 NSS300 Scooters for Rear Brake Line Leak
Honda is recalling 2014 NSS300 and NSS300A scooters because improperly tightened rear brake lines may leak fluid, reducing braking function and increasing crash risk.
Product
HONDA — HONDA NSS300
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V112000·2016-02-25
Open Range Journeyer Trailers Recalled for Underrated Safety Chains
Open Range is recalling 2012-2015 Journeyer trailers because the safety chains are not rated high enough to support the trailer's weight if the main connection fails.
Product
OPEN RANGE — OPEN RANGE JOURNEYER
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0672-2016·2016-02-24
Rhino 7 3000 Recalled for Undeclared Active Pharmaceutical Ingredients
Premiere Sales Group is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.
Product
Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0615-2016·2016-02-24
Wholesome Soy Products Recalls Mung Bean Sprouts Due to Listeria
Wholesome Soy Products is recalling mung bean sprouts because Listeria monocytogenes was found in the product and production area.
Product
Mung bean sprouts packaged in 10 lb., 15 lb., and 30 lb. plastic bags.
Category
Food
Distribution
1 state
CriticalFDA (Drugs)·D-0674-2016·2016-02-24
Medisca Recalls L-Citrulline API Due to Labeling Error
Medisca Inc is recalling L-Citrulline API bottles because FDA testing found the product contained N-acetyl-leucine instead of the labeled ingredient.
Product
CITRULLINE (L) in 25 g, 100 g, 500 g and 1 kg plastic bottles, White crystals or crystalline powder, odorless, For Use and distribution in prescription compounding, manufacturing, processing, or repackaging only in accordance with FDA regulations and applicable law, Packaged by…
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0671-2016·2016-02-24
Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients
MSNV, Inc dba National Video Supply is recalling Rhino 7 Platinum 3000 single blister packs because they contain undeclared active pharmaceutical ingredients.
Product
Rhino 7 Platinum 3000, Single Blister Packs, distributed By Rhino 7, Made in USA
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0669-2016·2016-02-24
Glades Drugs Recalls Vitamin D3 Supplement Due to Excessive Potency
Glades Drugs Inc. is recalling Vitamin D3 supplement capsules because they contain an extremely high level of vitamin D3.
Product
Vitamin Supplement (Vial) D3, (cholecalciferol (vit D3)/lipoic acid/ubiquinol/ methylcobalamin/pyridoxine/methionine/inositol/choline bitartrate USP) capsules, 60, 120 or 180 count vials, Glades Drugs, 109 S. Lake Ave., Pahokee, FL 33476.
Category
Drug
Distribution
2 states
CriticalFDA (Drugs)·D-724-2016·2016-02-24
Pharmedium Recalls Subpotent Fentanyl Citrate Syringes for IV Use
Pharmedium Services, LLC is recalling 500 syringes of fentanyl citrate because the drug was subpotent. The affected product was distributed to nine hospital pharmacies.
Product
fentaNYL Citrate, Preservative Free, 10 mcg per 1 mL In 0.9% Sodium Chloride, 1 mL Total Volume For IV Use, packaged in a 3 mL syringe, code 2R3174, PharMEDium
Category
Drug
Distribution
7 states
CriticalFDA (Drugs)·D-0667-2016·2016-02-24
APEXXX tablets recalled for containing unapproved sildenafil
Nuway Distributors is recalling APEXXX tablets because they contain sildenafil, an unapproved drug for erectile dysfunction.
Product
APEXXX tablets, 300 mg, packaged in 1-count blister cards, Distributed Exclusively by: Nuway Distributors, LLC, Orlando, FL USA; UPC 7 05105 96361 7.
Category
Drug
Distribution
Distributed nationwide

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