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

12126–12150 of 18028

ModerateFDA (Drugs)·D-1035-2016·2016-06-22
Valeant Recalls Chlordiazepoxide HCl/Clidinium Bromide Capsules Due to Impurities
Valeant Pharmaceuticals is recalling specific lots of Chlordiazepoxide HCl/Clidinium Bromide capsules because they failed impurities and degradation specifications.
Product
Chlordiazepoxide HCl/Clidinium Bromide capsules, 5 /2.5 mg, 100-count bottle, Rx Only, Manufactured in Canada by: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7 Canada; Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1031-2016·2016-06-22
Galderma Recalls Doxycycline Capsules Due to Missing Lot and Expiration Dates
Galderma Laboratories is recalling Doxycycline USP Capsules 40 mg because some bottles are missing lot numbers or expiration dates.
Product
Doxycycline, USP Capsules 40 mg, Packaged in 30 ct Bottles, Rx Only. Marketed by: Prasco Laboratories, Mason, OH 45040 USA, Manufactured by: Catalent Pharma Solutions, LLC, Winchester, Kentucky 40391. NDC: 66993-815-30.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1034-2016·2016-06-22
Valeant Recalls Librax Capsules Due to Failed Impurity Specifications
Valeant Pharmaceuticals is recalling specific lots of Librax capsules because they failed impurity and degradation specifications.
Product
LIBRAX — LIBRAX (CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1029-2016·2016-06-22
Genzyme Recalls Hectorol Injection Vials Due to Incorrect Barcode Labeling
Genzyme is recalling 2,350 vials of Hectorol (doxercalciferol) injection because the vial labels contain an incorrect barcode. The affected product was distributed to Michigan, Pennsylvania, and New Jersey.
Product
Hectorol (doxercalciferol injection) 2 mcg/1mL, Rx only, Manufactured by: Genzyme Biosurgery Corporation 500 Kendall Street, Cambridge, MA 02142, NDC 58468-0126-1
Category
Drug
Distribution
3 states
LowFDA (Drugs)·D-1036-2016·2016-06-22
Sandoz Recalls Lisinopril Tablets Due to Missing Package Insert
Sandoz Inc is recalling 3,048 bottles of Lisinopril Tablets USP, 30 mg, because the package insert is incorrect or missing.
Product
Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-0630-01
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0966-2016·2016-06-15
FDA Recalls Thin and Slim Thermogenic Fat Burner for Unapproved Ingredient
Novacare, LLC is recalling The Store Thin and Slim Thermogenic Fat Burner because FDA sampling found salicylic acid, an ingredient not approved for dietary supplements.
Product
The Store Thin and Slim Thermogenic Fat Burner Dietary Supplement packaged in 90 capsule containers. Distributed by The Store 2050 E. 6200 S., Holladay, UT 84121, The Store Holliday, 4695 S.Holladay Blvd, Holladay, UT 84117, The Store Midway, 42 W. Main Street, Midway, UT 84049.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0964-2016·2016-06-15
Novacare Recalls MetaPro 360 Supplement Containing Unapproved Salicylic Acid
Novacare, LLC is recalling MetaPro 360 Metabolic Accelerator dietary supplements because FDA sampling confirmed the presence of salicylic acid, an unapproved drug ingredient.
Product
MetaPro 360 Metabolic Accelerator Dietary Supplement packaged in 120 capsule containers. www.metapro360.com 877-778-7509.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0970-2016·2016-06-15
FDA Recalls Asia Black 25 Ephedra Extreme Fat Burner for Unapproved Ingredients
Novacare, LLC is recalling Asia Black 25 Ephedra Extreme Fat Burner because FDA sampling confirmed the presence of salicylic acid, an unapproved ingredient in dietary supplements.
Product
Asia Black 25 Ephedra Extreme Fat Burner Potent Dietary Supplement packaged in 100 capsule containers. Distributed by Cloma Pharma Laboratories, Samford, CT 06902.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0960-2016·2016-06-15
Fuel Up High Octane capsules recalled for undeclared sildenafil analogue
Reesna, Inc. is recalling Fuel Up High Octane capsules because they contain undeclared hydroxythiohomosildenafil, an analogue of the prescription drug Sildenafil.
Product
FUEL UP HIGH OCTANE, capsules, a) 1-count package, b) 5-count bottle, c) 10-count bottle WWW.FUELUPPILLS.COM
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0957-2016·2016-06-15
Baxter Recalls Sodium Chloride Injection Due to Insect Particulate Matter
Baxter Healthcare is recalling 255,852 bags of 0.9% Sodium Chloride Injection because customers reported finding an insect in the primary container.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0962-2016·2016-06-15
FDA Recalls Thermo FX Supplement for Unapproved Salicylic Acid
Novacare, LLC is recalling The People's Chemist Thermo FX Barely Legal Thermogenic Aid because FDA sampling confirmed the presence of salicylic acid in the product.
Product
The People's Chemist Thermo FX Barely Legal Thermogenic Aid, packaged in 90 capsule containers. Manufactured by TPC, LLC, www.thepeopleschemist.com.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0959-2016·2016-06-15
Fuel Up Plus capsules recalled for undeclared sildenafil analogue
Reesna, Inc. is recalling Fuel Up Plus capsules marketed as a dietary supplement because they contain undeclared hydroxythiohomosildenafil, an analogue of the ED drug sildenafil.
Product
FUEL UP PLUS, capsules, a) 1-count package, b) 5-count bottle, c) 10-count bottle WWW.FUELUPPILLS.COM
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1010-2016·2016-06-15
Well Care Compounding Pharmacy Recalls SUPER TRI-MIX #4 Due to Sterility Concerns
Well Care Compounding Pharmacy is recalling 869 vials of SUPER TRI-MIX #4 because FDA inspections found violations that may affect sterility.
Product
SUPER TRI-MIX #4, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-1025-2016·2016-06-15
Well Care Compounding Pharmacy Recalls QUAD-MIX #3 Due to Sterility Concerns
Well Care Compounding Pharmacy is recalling QUAD-MIX #3 vials because FDA inspections found violations that may affect product sterility.
Product
QUAD-MIX #3, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0965-2016·2016-06-15
FDA Recalls Thin and Slim Burn Fat Now Supplement for Unapproved Ingredient
Novacare, LLC is recalling Thin and Slim Burn Fat Now dietary supplements because FDA sampling confirmed the presence of salicylic acid, an unapproved drug ingredient.
Product
Thin and Slim Burn Fat Now Dietary Supplement packaged in 90 capsule containers. http://www.secretsofherbs.com. Made in the USA.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0988-2016·2016-06-15
FDA Recalls 1-HCG 1000 IU/ML Due to Sterility Concerns
Well Care Compounding Pharmacy is recalling 1-HCG 1000 IU/ML vials because FDA inspections identified GMP violations that may impact product sterility.
Product
1-HCG 1000 IU/ML, packaged in 5mL and 10mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0958-2016·2016-06-15
Baxter Recalls Dextrose Injection Due to Insect Contamination
Baxter Healthcare is recalling Dextrose Injection, USP, 70% due to confirmed reports of an insect found in the primary container.
Product
DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0963-2016·2016-06-15
FDA Recalls MaxOut Body Fat Burner for Unapproved Salicylic Acid
Novacare, LLC is recalling MaxOut Body Fat Burner with Ephedra because FDA sampling confirmed the presence of salicylic acid in the dietary supplement.
Product
Thin and Slim MaxOut Body Max Out FX Fat Burner with Ephedra packaged in containers of 60 capsules. Distributed by Teamtrade, Inc., Ft. Lauderdale, FL. 1-866-MaxOut www.MaxOutBODY.com.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1006-2016·2016-06-15
Well Care Compounding Pharmacy Recalls QUAD-MIX #1 Due to Sterility Concerns
Well Care Compounding Pharmacy is recalling QUAD-MIX #1 vials because FDA inspections found violations that may affect sterility.
Product
QUAD-MIX #1, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0984-2016·2016-06-15
Estradiol Valerate Recall Due to Sterility Assurance Concerns
Well Care Compounding Pharmacy is recalling Estradiol Valerate 40mg/mL vials because FDA inspections found GMP violations that may affect sterility.
Product
ESTRADIOL VALERATE 40MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0983-2016·2016-06-15
Estradiol Valerate Recall Due to Sterility Assurance Concerns
Well Care Compounding Pharmacy is recalling Estradiol Valerate 20mg/mL vials due to GMP violations affecting sterility.
Product
ESTRADIOL VALERATE 20MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-1027-2016·2016-06-15
FDA Recalls Itraconazole and Mupirocin Nasal Spray Due to Sterility Concerns
Well Care Compounding Pharmacy is recalling Itraconazole 0.2%/Mupirocin 0.2% Nasal Spray because FDA inspections found GMP violations that may affect sterility.
Product
ITRACONAZOLE 0.2%/MUPIROCIN 0.2% NASAL SPRAY; 30 mL Spray, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0985-2016·2016-06-15
Gentamicin Ophthalmic Solution Recalled for Sterility Assurance Concerns
Well Care Compounding Pharmacy is recalling Gentamicin 15 mg/ml Ophthalmic Solution due to FDA inspection findings regarding sterility assurance.
Product
GENTAMICIN 15 MG/ML Ophthalmic Solution, Sterile Droppers, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-1026-2016·2016-06-15
Well Care Compounding Pharmacy Recalls Otic Solution Due to Sterility Concerns
Well Care Compounding Pharmacy is recalling specific lots of Clotrimazole 1%/Betamethasone Dipropionate 0.05% Otic Solution because FDA inspections found GMP violations that may affect sterility.
Product
CLOTRIMAZOLE 1%/ BETAMETHASONE DIPROPIONATE 0.05% OTIC SOLUTION, 15mL dropper, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-1000-2016·2016-06-15
Methylcobalamin Injection Recalled Due to Sterility Assurance Concerns
Well Care Compounding Pharmacy is recalling Methylcobalamin 1 mg/mL vials because FDA inspections found GMP violations that may impact product sterility.
Product
METHYLCOBALAMIN 1 MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Category
Drug
Distribution
1 state

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12126–12150 of 18028