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 deaths or serious injuries are reported, 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

6026–6050 of 18015

ModerateFDA (Drugs)·D-1523-2020·2020-08-26
Calvin Scott Recalls Phendimetrazine Capsules Due to Packaging Deviation
Calvin Scott & Co. is recalling specific lots of Phendimetrazine capsules because light-sensitive products were repackaged in transparent pouches, violating CGMP standards.
Product
Phendimetrazine Brown/Clear Capsules, 105 mg, 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Virtus Pharm., LLC Newtown, PA 18940; NDC 69543-0409-11
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1532-2020·2020-08-26
Calvin Scott Recalls Phentermine Tablets Due to Packaging Defect
Calvin Scott & Company is recalling specific lots of Phentermine HCL 37.5 mg tablets because they were repackaged in transparent pouches, violating light-sensitivity requirements.
Product
Phentermine HCL Blue Speckled tablets, 37.5 mg, packaged in a) 14-count bags (NDC 10702-0025-10) and b) 28-count bags (NDC 10702-0025-10), Rx Only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: KVK-Tech., Inc Newtown, PA 18940.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1516-2020·2020-08-26
Calvin Scott Recalls Hydrochlorothiazide Tablets Due to Packaging Defect
Calvin Scott & Company is recalling Hydrochlorothiazide 50mg tablets because light-sensitive products were repackaged in transparent pouches, violating CGMP standards.
Product
Hydrochlorothiazide 50mg tablets, 14-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Accord Healthcare, Inc., Durham NC 27703; NDC 16729-0184-17
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1526-2020·2020-08-26
Calvin Scott Recalls Phentermine HCL Capsules Due to Packaging Defects
Calvin Scott & Company is recalling specific lots of Phentermine HCL capsules because light-sensitive products were repackaged in transparent pouches.
Product
Phentermine HCL GrayYellow capsules, 15mg, packaged in a) 28-count bags and b) 56-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: Tagi Pharma, South Beloit, IL 61080; NDC 51224-0203-70
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1529-2020·2020-08-26
Calvin Scott Recalls Phentermine Capsules Due to Packaging Defect
Calvin Scott & Co. is recalling Phentermine HCL capsules because light-sensitive products were repackaged in transparent pouches.
Product
Phentermine HCL Blue/White Capsules, 37.5 mg, 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: KVK-Tech., Inc Newtown, PA 18940; NDC 10702-0029-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1528-2020·2020-08-26
Calvin Scott Recalls Phentermine HCL Capsules Due to Packaging Defect
Calvin Scott & Company is recalling Phentermine HCL 30mg capsules because they were repackaged in transparent pouches, exposing the light-sensitive medication to potential degradation.
Product
Phentermine HCL Blue/Clear capsules, 30mg, packaged in a) 10-count bags (NDC 10702-0028-10), b) 28-count bags (NDC 10702-0028-10) and c) 56-count bags (NDC 10702-0028-10), Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by KVK-Tech Newtown, PA 18940;
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1519-2020·2020-08-26
Calvin Scott Recalls Thyroid Neutral Tabs Due to Packaging Deviation
Calvin Scott & Company is recalling Thyroid Neutral Tabs 2 gr because light-sensitive tablets were repackaged in transparent pouches, violating CGMP standards.
Product
Thyroid Neutral Tabs 2 gr, 28-count tablets, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, MN 87123, Manufactured by RLC, Cave Creek, AZ 85331 Labs, NDC 64727-3308-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1531-2020·2020-08-26
Calvin Scott Recalls Phentermine Tablets Due to Packaging Deviations
Calvin Scott & Company is recalling specific lots of Phentermine HCL tablets because they were repackaged in transparent pouches, violating CGMP requirements for light-sensitive drugs.
Product
Phentermine HCL White/Blue Speckled tablets, 37.5 mg, packaged in a) 7-count bags, and b) 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Lannett Company, Inc. Philadelphia, PA 19136; NDC 00527-1445-10
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1512-2020·2020-08-26
Ultra Seal Recalls Pain Relief Tablets Due to Stability Failures
Ultra Seal Corporation is recalling specific lots of Pain Relief Maximum Strength tablets because they failed stability specifications for salicylic acid.
Product
Pain Relief Maximum Strength (Acetaminophen 250 mg/aspirin 250 mg/Caffeine 65 mg) tablets, 2-tablets per packet, Manufactured for Select Corporation, Carrollton, TX 75007
Category
Drug
Distribution
2 states
LowFDA (Drugs)·D-1513-2020·2020-08-26
Ultra Seal Recalls Extra Strength Headache Relief Tablets for Stability Failures
Ultra Seal Corporation is recalling 701,735 packets of Extra Strength Headache Relief tablets due to out-of-specification results for salicylic acid.
Product
Extra Strength Headache Relief (Acetaminophen 250 mg/aspirin 250 mg/Caffeine 65 mg) tablets, 2-tablet packets, Manufactured for: Convenience Valet Glendale Heights, IL 60139,
Category
Drug
Distribution
2 states
CriticalFDA (Drugs)·D-1538-2020·2020-08-19
Itech 361 LLC Recalls All Clean Hand Sanitizer Due to Methanol
Itech 361 LLC is recalling 18,760 bottles of All Clean Hand Sanitizer because the product contains undeclared methanol.
Product
All Clean Hand Sanitizer, Fresh Scent, 1 Liter bottles, Ethyl Alcohol 70.00%, Produced by Eskbiochem SA de CV Ave Mexico Japon 50 Celaya, Gto. Mexico 38010, Distributed by All Clean Natural LTD, UPC Code 6 28055 37013 0
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1500-2020·2020-08-19
Eosera Recalls Ear Itch MD Anti-Itch Spray Due to cGMP Deviations
Eosera, Inc. is voluntarily recalling 43,424 bottles of Ear Itch MD Anti-Itch Spray due to cGMP deviations. The product was distributed nationwide in the United States.
Product
Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0071-5, UPC 851722007125
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1501-2020·2020-08-19
Eosera Recalls Ear Itch MD Sprays Due to Manufacturing Deviations
Eosera, Inc. is voluntarily recalling specific lots of Ear Itch MD sprays nationwide due to cGMP deviations.
Product
Day & Night Pack Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%), 0.5 FL OZ (15 mL) bottles/Ear Itch MD Nighttime Intensive Soothing Spray (pramoxine HCL 1%), 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0071-5
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1495-2020·2020-08-19
SCA Pharmaceuticals Recalls Heparin Sodium Bags Due to Low Potency
SCA Pharmaceuticals is recalling 3,932 bags of Heparin Sodium 5,000 units due to out-of-specification potency results at the 30-day stability timepoint.
Product
Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL bag (5 units/mL), Rx only, SCA Pharmaceuticals 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0650-46
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1499-2020·2020-08-19
Eosera Recalls Ear Pain MD Pain Relief Drops Due to cGMP Deviations
Eosera, Inc. is voluntarily recalling 125,874 bottles of Ear Pain MD Pain Relief Drops with 4% Lidocaine due to current Good Manufacturing Practice (cGMP) deviations.
Product
Ear Pain MD Pain Relief Drops with 4% Lidocaine (lidocaine HCl Monohydrate 4%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0072-2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1502-2020·2020-08-19
Lupin Recalls Mibelas 24 Fe Tablets Due to Impurity Test Failures
Lupin Pharmaceuticals is recalling Mibelas 24 Fe chewable tablets because they failed impurity specifications. The recall covers 560,922 pouches distributed nationwide.
Product
Mibelas 24 Fe (norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tablets) chewable,1 mg/0.02 mg/75 mg, Rx Only, Provides 24 days of active therapy, Pouch Contains one wallet of 28 tablets, NDC: 68180-911-11, Carton contains 3 wallets of 28 tablets each, NDC
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1496-2020·2020-08-19
Taro Recalls Clobetasol Propionate Cream Due to Content Uniformity Failure
Taro Pharmaceuticals is recalling specific lots of Clobetasol Propionate Cream 0.05% because the bulk material failed content uniformity testing.
Product
Clobetasol Propionate Cream USP, 0.05%, a) 15 g tube, NDC: 60429-902-15; b) 45 g tube, NDC: 60429-902-45, Rx Only, For External Use Only, Not for Ophthalmic Use, Mfd by: Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T 1C1, Marketed by: Golden State Medical Supply, Inc. C
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1498-2020·2020-08-19
Eosera Recalls Ear Pain MD Pain Relief Drops For Kids
Eosera, Inc. is voluntarily recalling 45,673 bottles of Ear Pain MD Pain Relief Drops For Kids due to cGMP deviations.
Product
Ear Pain MD Pain Relief Drops For Kids (lidocaine HCl Monohydrate 4%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0070-8
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1494-2020·2020-08-19
FDA Recalls Nystatin Oral Suspension Due to Subpotent Drug Levels
Pharmaceutical Associates, Inc. is recalling Nystatin Oral Suspension because it failed potency testing. Patients should consult their healthcare provider.
Product
NYSTATIN — NYSTATIN (NYSTATIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1492-2020·2020-08-19
Teva Recalls Lidocaine Patches Due to Missing Lot and Expiration Dates
Teva Pharmaceuticals is recalling Lidocaine 5% Patches because individual pouches are missing lot and expiration dates. The recall covers 28,596 cartons distributed nationwide.
Product
LIDOCAINE — LIDOCAINE (LIDOCAINE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1497-2020·2020-08-19
Golden State Medical Supply Recalls Clobetasol Propionate Cream Due to Content Uniformity Failure
Golden State Medical Supply Inc. is recalling specific lots of Clobetasol Propionate Cream, USP, 0.05% because the bulk material failed content uniformity testing.
Product
Clobetasol Propionate Cream, USP, 0.05%, packaged in a)15g Tubes (NDC 60429-902-15) and b) 45g Tubes (NDC 60429-902-45), Rx Only, Mfd. by: Taro Pharmaceuticals Inc. Brampton, Ontario, Canada, Marketed by: Golden State Medical Supply Inc. Camarillo, CA 93012.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1490-2020·2020-08-19
West-Ward Recalls Leucovorin Calcium Tablets With Incorrect Identification Code
West-Ward Columbus Inc. is recalling 2,300 bottles of Leucovorin Calcium 10 mg tablets because they are imprinted with the incorrect identification code.
Product
LEUCOVORIN CALCIUM — LEUCOVORIN CALCIUM (LEUCOVORIN CALCIUM)
Category
Drug
Distribution
2 states
CriticalFDA (Drugs)·D-1453-2020·2020-08-12
Hemp Extract Recalled for Undeclared Lead Contamination
Michigan Herbal Remedies is recalling 496 bottles of Made by Hemp 1000MG Hemp Extract due to elevated levels of undeclared lead.
Product
Made by Hemp 1000MG Hemp Extract, Strawberry Creme, 1 OZ (30 ML) bottles, Dist by: MHR Brands, Jenison, MI, UPC 8 02991 76554 4
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1477-2020·2020-08-12
Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead Contamination
Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract due to elevated levels of undeclared lead. Consumers should stop using the product.
Product
Tasty Drops, Hemp Oil Extract, Vanilla, 1500MG CBD,1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29086 6
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1464-2020·2020-08-12
Pathway To Wellness CBD Oil Recalled for Undeclared Lead Contamination
Michigan Herbal Remedies is recalling 100 bottles of Pathway To Wellness CBD Oil due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.
Product
Pathway To Wellness, CBD Oil, Premium Hemp Oil Drops, Natural, 1000MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Pathway to Wellness
Category
Drug
Distribution
Distributed nationwide

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6026–6050 of 18015