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

101–125 of 840

CriticalFDA (Drugs)·D-0253-2021·2021-02-24
Optimus Lubricants Hand Sanitizer Recalled for Methanol Contamination
Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.
Product
OPTIMUS LUBRICANTS Instant Hand Sanitizer, (ethyl alcohol 70%) 8.5 Fl. Oz. (250 mL) bottle, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477. UPC # 7 501799 115621
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0262-2021·2021-02-17
Apotex Recalls Enoxaparin Syringes Due to Labeling Mixup
Apotex Corp. is recalling Enoxaparin Sodium Injection syringes because some barrels may display incorrect concentration markings, posing a risk of dosing errors.
Product
Enoxaparin Sodium Injection, USP 120 mg/ 0.8 mL Single Dose Syringes with Automatic Safety Device For Subcutaneous Injection 10 x 0.8 mL Single Dose Syringes Rx Only,Manufactured by: Gland Pharma Ltd. Hyderabad, India Manufactured for: Apotex Corp. Weston, FL 33326 NDC 60505-079
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0218-2021·2021-01-06
Wishgarden Herbs Recalls Happy Ducts Compress Due to Microbial Contamination
Wishgarden Herbs is recalling 46 jars of Happy Ducts Compress because the product tested positive for Cronobacter Sakazakii.
Product
Happy Ducts Compress, 3 oz. plastic jar, www.wishgardenherbs.com, Boulder, CO. 80301. UPC 6 56490 20223 5
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0220-2021·2021-01-06
WishGarden Herbs Recalls Goldenseal Powder Jars Due to Microbial Contamination
WishGarden Herbs is recalling 298 jars of Goldenseal Powder because testing found Cronobacter Sakazakii contamination.
Product
Goldenseal POWDER, 0.25 oz. (7 g) plastic jars, WishGarden Herbs, Inc., Boulder, CO 80301. UPC 6 56490 64137 9
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0168-2021·2020-12-23
AvKare Recalls Trazodone Hydrochloride Tablets Due to Sildenafil Packaging Mix-Up
AvKare Inc. is recalling 14,368 bottles of Trazodone Hydrochloride Tablets 100 mg because they were inadvertently packaged with sildenafil.
Product
TraZODONE Hydrochloride Tablets USP 100 mg, Rx Only, 1000-count Bottle, Manufactured for: AvKARE Pulaski, TN 38478, NDC 42291-834-10
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0118-2021·2020-12-09
MPM Medical Recalls REGENECARE HA Topical Anesthetic Due to Bacteria
MPM Medical LLC is recalling REGENECARE HA topical anesthetic hydrogel because it was found to be contaminated with Burkholderia cepacia bacteria.
Product
REGENECARE HA — REGENECARE HA (LIDOCAINE HCL)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0111-2021·2020-12-09
Lohxa Recalls Chlorhexidine Gluconate Oral Rinse Due to Bacterial Contamination
Lohxa LLC is recalling Chlorhexidine Gluconate Oral Rinse USP, 0.12%, due to contamination with Burkholderia lata bacteria.
Product
Chlorhexidine Gluconate Oral Rinse USP, 0.12%, Alcohol Free, packaged in 15 mL unit does cups (barcode 7016602715), packaged in 50-count unit dose cups per carton, Rx only, Distributed by: Lohxa, Worcester, MA 01608, NDC 70166-027-15
Category
Drug
Distribution
2 states
CriticalFDA (Drugs)·D-0035-2021·2020-10-28
Acella Recalls NP Thyroid 15 Tablets Due to Subpotent Levothyroxine
Acella Pharmaceuticals is recalling NP Thyroid 15 tablets because FDA analysis found the levothyroxine content was less than the labeled claim.
Product
NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0031-2021·2020-10-07
Blumen Hand Sanitizer Recalled for Methanol and Low Ethanol Content
4e Brands North America is recalling Blumen Advanced Hand Sanitizer because testing found methanol contamination and ethanol levels below the labeled claim.
Product
blumen ADVANCED HAND SANITIZER 70% ALCOHOL CONTENT, (ethyl alcohol 70% v/v) Packaged as a) 3.4 fl oz / 100 ml bottle, UPC 8 14266 02359 4, b) 7.5 fl oz / 221 ml bottle, UPC 8 14266 02362 4, Distributed in USA and Canada By: 4e Brands Northamerica LLC, 17806 IH-10W, Suite 300, Sa
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0030-2021·2020-10-07
blumen Hand Sanitizer Recalled for Methanol Contamination and Low Ethanol
4e Brands North America is recalling blumen hand sanitizer bottles due to methanol contamination and ethanol levels below the labeled claim.
Product
blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% natural boost with tea tree oil (70% ethyl alcohol), 33.8 fl oz / 1 L bottle, Distributed in USA and Canada by: 4e Brands 4e Brands Northamerica LLC. 17806 IH-10W, Suite 300, San Antonio, Texas, 78257. Made in Mexico.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0033-2021·2020-10-07
Volu-Sol Handrub Sanitizing Solution Recalled for Unapproved Marketing
Volu-Sol, Inc. is recalling handrub sanitizing solution marketed without an approved NDA/ANDA and listing methanol as an inactive ingredient.
Product
Volu-Sol Handrub Sanitizing Solution (Ethyl Alcohol, 69% v/v and Isopropyl Alcohol, 7.2% v/v) Topical Solution, 473 mL/ 16 fl oz bottle, Vou-Sol 5095 W 2100 S, Salt Lake City, UT 84120, NDC 74401-800-16
Category
Drug
Distribution
2 states
CriticalFDA (Drugs)·D-0029-2021·2020-10-07
Blumen Hand Sanitizer Recalled for Methanol and Low Alcohol Content
4e Brands North America is recalling Blumen hand sanitizer bottles and pumps found to contain methanol and less ethanol than labeled.
Product
blumen Clear ADVANCED HAND SANITIZER with 70% ALCOHOL, (ethyl alcohol 70% v/v), Packaged as a) 2 fl oz / 60 ml bottle, UPC 8 14266 02371 6 b) 17 fl oz / 503 ml bottle with blue cap or pump bottle, UPC 8 14266 02409 6 c) 33.8 fl oz / 1 L straight or curved bottle, UPC 8 14266 0236
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1595-2020·2020-09-30
Protein Shoppe Recalls Red-E Tablets Tainted With Sildenafil
The Protein Shoppe is recalling Red-E Tablets found to contain sildenafil, an unapproved drug for erectile dysfunction. The product was marketed without FDA approval.
Product
Red-E Tablet, Proprietary Blend 3000 mg**, packaged in 1-count plastic bag stapled with cardboard labeling.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1587-2020·2020-09-30
Gelbac T Hand Gel Recalled for Methanol Contamination
Incredible Products is recalling Gelbac T Antibacterial Hand Gel because it contains methanol and is sub-potent for ethanol.
Product
Incredible Products Gelbac T Antibacterial Hand Gel (ethyl alcohol 80%), Kills 99.9% bacteria and germs, a) 4.2 Oz./125 mL bottle, NDC: 71761-000-00, UPC: 7502278002555, Distributed by Pacific Coast Global Inc. Chula Vista, CA 91911, Made in Mexico b) 33.8 Oz./1 L, UPC: 750227800
Category
Drug
Distribution
2 states
CriticalFDA (Drugs)·D-1615-2020·2020-09-23
RLC Labs Recalls Subpotent Nature Throid Thyroid Medication
RLC Labs Inc. is recalling Nature Throid thyroid medication because FDA analysis found the product to be subpotent.
Product
Nature Throid, 1/2 Grain (32.5 mg) Thyroid USP [Liothyronine (T3) 4.5 mcg, Levothyroxine (T4) 19 mcg], packaged in a) 90-count bottles (NDC 64727-3299-6), b) 100-count bottles (NDC 64727-3299-1), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1583-2020·2020-09-23
Born Basic Hand Sanitizer Recalled for Methanol Contamination
Real Clean Distribuciones SA de CV is recalling Born Basic Anti-Bac Hand Sanitizer because it contained methanol and had lower ethanol levels than labeled.
Product
BORN BASIC., ANTI-BAC HAND SANITIZER, 70% Alcohol, (Ethyl Alcohol 70%), 16.9 FL OZ (500 mL) bottle, UPC 8 40038 21456 3, Made in Mexico; Distributed by Scent Theory Products, LLC, New York, NY 10018.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1619-2020·2020-09-23
RLC Labs Recalls Subpotent Nature Throid Thyroid Medication
RLC Labs Inc. is recalling Nature Throid 1.5 Grain thyroid medication because FDA analysis found the product to be subpotent.
Product
Nature Throid, 1.5 Grain (97.5 mg) Thyroid USP [Liothyronine (T3) 13.5 mcg, Levothyroxine (T4) 57 mcg], packaged in a) 30-count bottles (NDC 64727-3305-4), b) 60-count bottles (NDC 64727-3305-5), c) 90-count bottles (NDC 64727-3305-6), and 100-count bottles (NDC 64727-3305-1), R
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1578-2020·2020-09-23
Herbacil Hand Sanitizer Recalled for Methanol Contamination and Low Ethanol
Broncolin, S.A. de C.V. is recalling Herbacil Antiseptic Hand Sanitizer because it contained methanol and had lower ethanol levels than labeled.
Product
HERBACIL, Antiseptic Hand Sanitizer, 70% Alcohol, (Alcohol) 70%, packaged as a) 4.22 fl. oz. (125ml) bottle, UPC 7 14706 91368 6; b) 8.4 fl. oz. (250 ml) bottle, UPC 714706 91367 9; c) 33.8 fl. oz. (1 Liter) bottle, UPC 7 14706 91365 5; , Made in Mexico by: Broncolin, S.A. de C.V
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1584-2020·2020-09-23
Maison Terre Goldenseal Root Powder Recalled for Microbial Contamination
Maison Terre, LLC is recalling Goldenseal Root Powder Organic due to FDA findings of contamination with various microorganisms, including Cronobacter sakazakii.
Product
Goldenseal Root Powder Organic, 1 oz. clear plastic bag, Maison Terre Natural Products, www.maisonterre.net
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1574-2020·2020-09-09
FDA Recalls Skin Guard 24 Hand Sanitizing Towelettes for Unapproved Methanol
SG24 LLC is recalling Skin Guard 24 hand sanitizing towelettes because they contain unapproved methanol and lack FDA approval.
Product
Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Towelette packaged in 2.5 x 3.75 packets, Dist by: SG24 LLC, Bolingbroke, GA 31004
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1570-2020·2020-09-09
Hand Sanitizer Recalled for Methanol Contamination
AAA Cosmetica is recalling bio aaa Advance Hand Sanitizer because it contains methanol. Consumers should stop using the product.
Product
bio aaa Advance Hand Sanitizer Ethyl Alcohol 70%, Unscented, 16.23 Oz (480 mL), Distributed By: Payless Janitorial Corporation 1341 SW 21 Terrance, Fort Lauderdale, Florida Exported By: E. Audicode S.A. de C.V. Manufactured By: AAA Cosmetica S.A. de C.V. UPC 7 502272 12111 5
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1575-2020·2020-09-09
Mylan Recalls Amiodarone Hydrochloride Injection Due to Labeling Mix-Up
Mylan Institutional LLC is recalling Amiodarone Hydrochloride Injection due to a labeling error where cartons may contain the wrong medication.
Product
AMIODARONE HYDROCHLORIDE — AMIODARONE HYDROCHLORIDE (AMIODARONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1576-2020·2020-09-09
Mylan Recalls Tranexamic Acid Injection Due to Labeling Mix-Up
Mylan Institutional LLC is recalling 1,407 cartons of Tranexamic Acid Injection due to a labeling error that may result in the wrong medication being dispensed.
Product
TRANEXAMIC ACID — TRANEXAMIC ACID (TRANEXAMIC ACID)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1534-2020·2020-09-02
Medichem Recalls Chlorhexidine Gluconate Due to Serratia marcescens Contamination
Medichem S.A. is recalling Chlorhexidine Gluconate 0012 for manufacturing due to microbial contamination with Serratia marcescens.
Product
Chlorhexidine Gluconate 0012 For Manufacturing, Processing or Repacking, RX Only, Medichem, S.A. Poligono Industrial Celra, 17460, Celra, Girona (Spain/Espana); Fructuos Gelabert, 6-8, 08970, Sant Joan Despi, Barcelona (Spain/Espana) NDC 53296-0012-0
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1551-2020·2020-09-02
SCA Pharmaceuticals Recalls Heparin Sodium Injection Due to Cross Contamination
SCA Pharmaceuticals is recalling 366 containers of Heparin Sodium 5,000 units in 0.9% Sodium Chloride 500 mL due to cross-contamination with undeclared benzyl alcohol.
Product
Heparin Sodium 5,000 units in 0.9% Sodium Chloride 500 mL, Single Dose Container, Rx Only Injection for Intravenous Use (10 units/mL), SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC#: 70004-0650-44, Bar Code 70004065044.
Category
Drug
Distribution
Distributed nationwide

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