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

11401–11425 of 36636

SevereFDA (Drugs)·D-1097-2020·2020-04-15
Innovative Compounding Pharmacy Recalls Hydroxyprogesterone Caproate Due to Sterility Concerns
Innovative Compounding Pharmacy is recalling Hydroxyprogesterone Caproate injections because the FDA cannot ensure the product is sterile. Patients in California, Maine, and Texas should stop using the medication.
Product
Hydroxyprogesterone Caproate (BUD) 350mg/ml , 4 mL, Injectable, Rx only, INNOVATIVE COMPOUNDING PHARMACY, 41536 EASTMAN DRIVE SUITE A MURRIETA , CA 92562 951-304-9530
Category
Drug
Distribution
3 states
SevereFDA (Drugs)·D-1087-2020·2020-04-15
PharMEDium Recalls Rocuronium Bromide Syringes Due to Sterility Assurance Issues
PharMEDium Services, LLC is recalling 46 lots of rocuronium bromide syringes because of a lack of sterility assurance. The products were distributed nationwide in the US.
Product
rocuronium Bromide, 10 mg per mL, 50 mg per 5 mL, 5 mL BD Syringe, for IV Use, PharMEDium 13N. Davis Ave. Cleveland MS 36732. NDC 71019-321-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1133-2020·2020-04-15
Herbal Doctor Remedies Recalls Herpes Off Due to Unapproved New Drug Status
Herbal Doctor Remedies is recalling Herpes Off because the product is misbranded as an unapproved new drug. The product was sold online in the U.S. and internationally.
Product
Herpes Off, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
0 states
SevereFDA (Drugs)·D-1131-2020·2020-04-15
FDA Recalls Hernia Off for Unapproved New Drug Status
Herbal Doctor Remedies is recalling Hernia Off because the product is misbranded as an unapproved new drug.
Product
Hernia Off, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
0 states
SevereFDA (Drugs)·D-1096-2020·2020-04-15
Innovative Compounding Pharmacy Recalls MIC-8 Injectable Due to Sterility Concerns
Innovative Compounding Pharmacy is recalling MIC-8 injectable vials because the firm cannot assure the product's sterility. Patients in California, Maine, and Texas should stop using the product.
Product
MIC-8 (Methionine 15mg /Inositol 50 mg/Choline 100 mg/B-12 6mcg/ml) , 10 mL, Injectable, Rx only, INNOVATIVE COMPOUNDING PHARMACY, 41536 EASTMAN DRIVE SUITE A MURRIETA , CA 92562 951-304-9530
Category
Drug
Distribution
3 states
SevereFDA (Drugs)·D-1101-2020·2020-04-15
Teva Recalls Losartan Potassium Tablets Due to NMBA Impurity
Teva Pharmaceuticals USA is recalling bulk Losartan Potassium Tablets 50 mg because an impurity, NMBA, was detected in the active pharmaceutical ingredient.
Product
LOSARTAN POTASSIUM TABLETS, USP 50 mg, Bulk, Rx only, For Further Manufacturing, Packing or Repackaging only, Manufactured by: Arrow Pharma (Malta) Ltd., Birzebbugia, Malta NDC 0591-3746-00
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-1102-2020·2020-04-15
Teva Recalls Losartan Potassium Tablets Due to NMBA Impurity
Teva Pharmaceuticals USA is recalling bulk Losartan Potassium Tablets 100 mg because an impurity called NMBA was detected in the active ingredient.
Product
LOSARTAN POTASSIUM TABLETS, USP 100 mg, Bulk, Rx only, For Further Manufacturing, Packing or Repackaging only, Manufactured by: Arrow Pharma (Malta) Ltd., Birzebbugia, Malta NDC 0591-3747-00
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-1093-2020·2020-04-15
PharMEDium Recalls Fentanyl Citrate Injection Due to Sterility Assurance Issues
PharMEDium Services, LLC is recalling 46 lots of fentanyl citrate injection products because of a lack of sterility assurance.
Product
fentaNYL Citrate Injection 50 mcg per mL, 100 mcg per 2 mL, 2 mL per syringe, For IV Use, Rx Only, PharMEDium Services, LLC 913 N. Davis Ave Cleveland, MS 05810. NDC 61553-303-28
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1095-2020·2020-04-15
Innovative Compounding Pharmacy Recalls Methylcobalamin Injectable Due to Sterility Concerns
Innovative Compounding Pharmacy is recalling specific lots of Methylcobalamin Injectable due to a lack of assurance of sterility. Patients in California, Maine, and Texas should stop using the product.
Product
Methylcobalamin Soln. 1000 mcg/ml, 10 mL, Injectable, Rx only, INNOVATIVE COMPOUNDING PHARMACY, 41536 EASTMAN DRIVE SUITE A MURRIETA , CA 92562 951-304-9530
Category
Drug
Distribution
3 states
SevereFDA (Drugs)·D-1085-2020·2020-04-15
PharMEDium Recalls Fentanyl Citrate Infusions Due to Sterility Assurance Issues
PharMEDium Services, LLC is recalling 46 lots of fentanyl citrate infusions because of a lack of sterility assurance. The products were distributed nationwide in the US.
Product
fentaNYL Citrate 10 mcg per mL, 2,500 mcg per 250 mL, 250 mL in a LifeCare Bag, in Sodium Chloride 0.9%. Rx Only, PharMEDium Services, LLC 913 N. Davis Ave Cleveland, MS 36732 NDC 61553-113-50
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20E022000·2020-04-13
Takata Driver Air Bag Inflator Recall for Honda and Nissan Vehicles
Honda and Nissan are recalling vehicles with Takata driver air bag inflators that may explode during deployment, posing a risk of serious injury or death.
Product
AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·007-2020·2020-04-10
Conagra Recalls Frozen Chicken Bowls Due to Possible Rock Contamination
Conagra Brands is recalling approximately 130,763 pounds of frozen Healthy Choice Chicken Feta & Farro bowls because they may contain small rocks.
Product
Conagra Brands (Conagra Foods Packaged Foods, LLC) — Conagra Brands, Inc. Recalls Frozen Not-Ready-to-Eat Chicken Bowl Products Due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
SevereUSDA FSIS·008·2020-04-10
Jowett Farms Recalls Pork Sausage Products Lacking Import Inspection
Jowett Farms is recalling approximately 42,587 pounds of raw pork trimmings and processed sausage products that were not presented for import re-inspection into the United States.
Product
Jowett Farms Corporation Recalls Pork Products Produced without Benefit of Import Inspection
Category
Food
Distribution
2 states
SevereNHTSA·20V213000·2020-04-09
Hyundai Recalls 2020 Nexo and Sonata for Parking Software Defect
Hyundai is recalling 2020 Nexo and Sonata vehicles because a software defect in the Remote Smart Parking Assist system may allow unintended vehicle movement, increasing crash risk.
Product
HYUNDAI — HYUNDAI SONATA, NEXO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V209000·2020-04-09
Forest River Recalls 2021 Starcraft Bus All Star Over Wiring Chafing
Forest River is recalling 2021 Starcraft Bus All Star transit buses because a wire harness may chafe against the frame, potentially causing engine stalls or loss of braking stability.
Product
STARCRAFT BUS — STARCRAFT BUS ALL STAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V210000·2020-04-09
StarCraft Starquest School Bus Recall for Wire Harness Chaffing
Forest River is recalling 2022 StarCraft Starquest school buses because a wire harness may chafe against the frame, potentially causing engine stalls or loss of braking stability.
Product
STARCRAFT BUS — STARCRAFT BUS STARQUEST
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V207000·2020-04-09
RAM 2500 and 3500 Trucks Recalled for Bed Step Failure Risk
Chrysler is recalling 2019-2020 RAM 2500 and 3500 trucks because the accessory bed step may fail during use, increasing injury risk.
Product
RAM — RAM 3500, 2500
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0910-2020·2020-04-08
Guan's Enoki Mushrooms Recalled Due to Listeria monocytogenes Contamination
Forest Mushroom Food Inc. is recalling Guan's Enoki Mushrooms after California health officials detected Listeria monocytogenes in retail samples.
Product
Guan's Enoki Mushrooms; Net Weight 200 g - 7.05 oz. UPC: 8 59267007013 Product Number:50130 Product of Korea, Keep refrigerated Distributed by Guan's Mushroom Co. Los Angeles, CA Package is clear plastic top with Guan's logo, green bottom with Enoki Mushroom in…
Category
Food
Distribution
8 states
CriticalFDA (Drugs)·D-1080-2020·2020-04-08
Natural Remedies Active Male Formula Recalled for Undeclared Tadalafil
FDA is recalling Natural Remedies Active Male 500 mg dietary supplements because they contain undeclared Tadalafil, an FDA-approved drug for erectile dysfunction.
Product
Natural Remedies Active Male 500 mg Male Pleasure Formula Dietary Supplement Manufactured For: Natural Remedies San Antonio, TX, USA 1(877)543-3501
Category
Drug
Distribution
2 states
SevereNHTSA·20V202000·2020-04-08
Great Dane Recalls 2020-2021 Everest Vans Due to Axle Nut Clip Defect
Great Dane is recalling 2020-2021 Everest Refrigerated Vans because improperly installed axle nut retaining clips may cause loose wheels and loss of vehicle control.
Product
GREAT DANE — GREAT DANE EVEREST
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V203000·2020-04-08
Spartan Gladiator and MetroStar Recalled for Park Brake Line Defect
Marion Body Works is recalling 2019-2020 Spartan Gladiator and MetroStar vehicles because the park brake control line may loosen, potentially causing sudden deceleration and increasing crash risk.
Product
SPARTAN — SPARTAN METROSTAR, GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V206000·2020-04-08
Vac-Tron Vacuum Excavator Trailers Recalled for Rear Impact Protection Defect
Vac-Tron is recalling 2012-2020 vacuum excavator trailers because they may lack extended lower chassis, reducing rear impact protection and increasing crash risk.
Product
VAC-TRON — VAC-TRON MINICOMBO, MC 873 SDT, MC 835 SDT, MC 833 SDT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20E019000·2020-04-08
Agility Fuel Solutions Recalls CNG Pressure Relief Devices for Rupture Risk
Agility Fuel Solutions is recalling certain CNG pressure relief devices that may fail to vent when exposed to heat, potentially causing the fuel system to rupture.
Product
FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY:PRESSURE RELIEF DEVICES recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1071-2020·2020-04-08
Par Pharmaceutical Recalls Glycopyrrolate Tablets Due to Unknown Impurity
Par Pharmaceutical is recalling 29,352 bottles of Glycopyrrolate Tablets, USP 1 mg, because an unknown impurity was detected.
Product
Glycopyrrolate Tablets, USP 1 mg, 100-count bottle, Rx only, Dist. by: Par Pharmaceutical, Chestnut Ridge, NY, 10977, U.S.A, Mfg. by: Par Formulations Private Limited, 1/58, Pudupakkam, Kelambakkam - 603 103., Made in India NDC# 49884-0065-01
Category
Drug
Distribution
0 states
SevereFDA (Devices)·Z-1622-2020·2020-04-08
Philips V60 Ventilators Recalled for Power Management Board Failure
Respironics is recalling 23,581 Philips V60 Ventilators because a solder connection failure on the power board may cause the blower to lose power or shut down unexpectedly, potentially leading to hypercarbia or hypoxemia.
Product
Philips V60 Ventilators with Power Management PCBA part number 1055906
Category
Medical Device
Distribution
53 states

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