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

5126–5150 of 17964

SevereFDA (Drugs)·D-0676-2021·2021-07-28
Goose Creek Hand Sanitizer Spray Recalled for Chemical Contamination
Goose Creek Hand Sanitizer aloe Champagne Bubbles spray (3.38 FL. OZ.) has been recalled because it is contaminated with methanol, benzene, and acetaldehyde. Consumers should stop using the product immediately.
Product
Goose Creek Hand Sanitizer aloe Champagne Bubbles, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 18489 01334 9
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0674-2021·2021-07-28
Goose Creek Hand Sanitizer recalled for methanol and benzene contamination
Goose Creek Hand Sanitizer aloe Beach Dreams spray (3.38 FL. OZ.) is being recalled because it is contaminated with methanol, benzene, and acetaldehyde. The product was distributed nationwide.
Product
Goose Creek Hand Sanitizer aloe Beach Dreams, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandles.com, 1498 S. Wallace Wilkinson Blvd. Liberty, KY 42539, UPC 8 18489 01336 3
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0688-2021·2021-07-28
69MODE Blue 69 Capsules Recalled for Undeclared Drug Ingredients
Nuri Trading LLC is recalling 69MODE Blue 69 capsules nationwide because they contain undeclared tadalafil and sildenafil, two FDA-approved drugs, making the product an unapproved drug without established safety or efficacy.
Product
69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0669-2021·2021-07-28
SS Lavender & Herbs Scented Sanitizer Recalled for Chemical Contamination
Scentsational Soaps & Candles Inc is recalling SS Lavender & Herbs Scented Sanitizer due to contamination with methanol, benzene, and acetaldehyde. The affected product was distributed nationwide.
Product
SS Lavender & Herbs Scented Sanitizer, Alcohol Antiseptic 70%, Non-sterile Topical Solution, 3.38 FL. OZ. (100 mL) a) Black and White Collection; b) Photo Real Collection
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0692-2021·2021-07-28
Compounded Semorelin/Ipamorelin Injection Recalled for Sterility Assurance
Innoveix Pharmaceuticals is recalling 728 vials of compounded Semorelin/Ipamorelin 3 mg injection due to lack of assurance of sterility. The affected lots are SIP215, SIP220, and SIP210.
Product
Compounded Lyophilized Semorelin/Ipamorelin 3 mg For subcutaneous or intramuscular injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0672-2021·2021-07-28
Goose Creek Hand Sanitizer Recalled for Chemical Contamination
Goose Creek Hand Sanitizer aloe Blueberry Limeade spray has been recalled due to contamination with methanol, benzene, and acetaldehyde. The product should not be used.
Product
Goose Creek Hand Sanitizer aloe Blueberry Limeade, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd. Liberty, KY 42539, UPC 8 14630 02049 5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0668-2021·2021-07-28
SS Eucalyptus Mint Scented Sanitizer Recalled for Chemical Contamination
Scentsational Soaps & Candles Inc is recalling SS Eucalyptus Mint Scented Sanitizer due to contamination with methanol, benzene, and acetaldehyde. The affected product was distributed nationwide.
Product
SS Eucalyptus Mint Scented Sanitizer, Alcohol Antiseptic 70%, Non-sterile Topical Solution, 3.38 FL. OZ. (100 mL), a) Black and White Collection; b) Photo Real Collection
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0673-2021·2021-07-28
Goose Creek Hand Sanitizer Recalled for Chemical Contamination
Goose Creek Hand Sanitizer aloe Limoncello (100 mL) is being recalled because the product contains methanol, benzene, and acetaldehyde. Consumers should stop using the product immediately.
Product
Goose Creek Hand Sanitizer aloe Limoncello, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL),Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd. Liberty, KY 42539, UPC 8 18489 01333 2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0678-2021·2021-07-28
Goose Creek Hand Sanitizer Recalled for Chemical Contamination
Goose Creek Hand Sanitizer aloe Marshmallows (3.38 FL. OZ.) is recalled nationwide due to contamination with methanol, benzene, and acetaldehyde. Consumers should stop using the product immediately.
Product
Goose Creek Hand Sanitizer aloe Marshmallows, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 18489 01331 8
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0670-2021·2021-07-28
SS Lemon Zest Scented Sanitizer contaminated with methanol and benzene
Scentsational Soaps & Candles Inc is recalling SS Lemon Zest Scented Sanitizer due to contamination with methanol, benzene, and acetaldehyde. The affected product was distributed nationwide.
Product
SS Lemon Zest Scented Sanitizer, Alcohol Antiseptic 70%, Non-sterile Topical Solution, 3.38 FL. OZ. (100 mL) a) Black and White Collection; b) Photo Real Collection
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0681-2021·2021-07-28
Goose Creek Hand Sanitizer Recalled for Chemical Contamination
Goose Creek Hand Sanitizer aloe Red, White & Blue Anti-Bacterial Spray (3.38 FL. OZ.) is being recalled nationwide because it is contaminated with methanol, benzene, and acetaldehyde.
Product
Goose Creek Hand Sanitizer aloe Red, White & Blue Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 14630 02045 7
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0684-2021·2021-07-28
Coconut Stand CoCo TKO Hand Sanitizer Contaminated with Methanol, Benzene, Acetaldehyde
Scentsational Soaps & Candles Inc is recalling Coconut Stand CoCo TKO Hand Sanitizer due to contamination with methanol, benzene, and acetaldehyde. The product was distributed nationwide in 3.4 FL. OZ. bottles.
Product
Coconut Stand CoCo TKO Hand Sanitizer, Totally Knocks Out 99.9% of Germs, 3.4 FL. OZ. (100.55 mL), Distributed by: Beauty Sparks LLC St. Petersburg, FL 33711
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0693-2021·2021-07-28
Compounded Lyophilized AOD-9604 Injection Recalled for Sterility Risk
Innoveix Pharmaceuticals is recalling compounded lyophilized AOD-9604 3 mg injection vials nationwide due to lack of assurance of sterility. The affected product was distributed as Rx-only injectable medication.
Product
Compounded Lyophilized AOD-9604, 3 mg For subcutaneous or intramuscular injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0675-2021·2021-07-28
Goose Creek Hand Sanitizer Spray Recalled for Chemical Contamination
Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer aloe Grape Soda spray because it contains methanol, benzene, and acetaldehyde. The contaminated product was distributed nationwide.
Product
Goose Creek Hand Sanitizer aloe Grape Soda, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 18489 01328 8
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0666-2021·2021-07-28
Ulta Beauty Hand Sanitizer Spray Recalled for Chemical Contamination
Ulta beauty Fresh Lemon Citron Frais Hand Sanitizer Spray is being recalled because the product contains methanol, benzene, and acetaldehyde. Affected lot numbers are 20357A, 20358B, and 20363C with expiration date 12/1/2022.
Product
Ulta beauty Fresh Lemon Citron Frais, 70% Alcohol Hand Sanitizer Spray, Net Wt. 100.55/3.4 fl. oz., UPC 717897092017
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0680-2021·2021-07-28
Goose Creek Hand Sanitizer Contaminated With Methanol, Benzene, Acetaldehyde
Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer aloe Optimistic Vibes spray due to contamination with methanol, benzene, and acetaldehyde. The product was distributed nationwide.
Product
Goose Creek Hand Sanitizer aloe Optimistic Vibes, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 14630 02234 5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0687-2021·2021-07-28
Thumbs Up 7 White Capsules Recalled for Undeclared Pharmaceutical Ingredients
Nuri Trading LLC is recalling Thumbs Up 7 White 11K capsules nationwide because they contain undeclared prescription drug ingredients (tadalafil, sildenafil, and vardenafil) and lack FDA approval.
Product
Thumbs Up 7 White 11K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0690-2021·2021-07-28
Erythromycin Topical Gel 2% Recalled Due to Failed Impurity Specifications
Teligent Pharma, Inc. is recalling Erythromycin Topical Gel 2% due to failed impurities and degradation specifications. The recall affects approximately 22,824 tubes distributed nationwide.
Product
Erythromycin Topical Gel, 2%, Net Wt. (a) 30 g,(NDC 52565-033-30) (b) 60 g,(NDC 52565-033-60) Rx Only, Manufactured by: Teligent Pharma, Inc. , Buena, NJ 08310,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0689-2021·2021-07-28
Erythromycin Topical Solution 2% Recalled for Failed Impurities Specifications
Teligent Pharma, Inc. is recalling Erythromycin Topical Solution USP 2% (60 mL, Lot 14180) distributed nationwide because it failed impurities and degradation specifications.
Product
Erythromycin Topical Solution USP, 2% 60 mL, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310, NDC 52565-027-59
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0665-2021·2021-07-28
Acetaminophen Extra Strength tablets recalled for incorrect enteric-coated labeling
LNK International is recalling Acetaminophen Extra Strength coated tablets because the primary label incorrectly states "enteric coated" when the tablets are not enteric coated and should be labeled as standard coated tablets.
Product
Acetaminophen EXTRA STRENGTH Pain Reliever / Fever Reducer, Enteric Coated, 50 Coated Tablets/ 500 mg each, Distributed by Amerisource Bergen, 1300 Morris Drive, Chesterbrook, PA, 19087, NDC 46122-649-71
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0657-2021·2021-07-21
Durisan Hand Sanitizing Wipes Recalled for Microbial Contamination
Sanit Technologies is recalling Durisan Antimicrobial Solutions Hand Sanitizing Wipes because certain lots were found to contain Burkholderia contaminans and/or yeast and mold through internal testing.
Product
Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing Wipes, 0.13%, 160-count canister; Sanit Technologies, LLC, 7810 25th Court East, Sarasota, Florida 34243, UPC 8 52379 00631 8.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0654-2021·2021-07-21
Poseidon Platinum 3500 Capsules Recalled for Undeclared Prescription Drugs
Poseidon Platinum 3500 capsules are being recalled because they contain undeclared sildenafil and tadalafil, which are prescription drugs that were not approved for this product. The safety and efficacy of these undeclared ingredients have not been established.
Product
Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Category
Drug
Distribution
0 states
SevereFDA (Drugs)·D-0694-2021·2021-07-21
Prairie Wolf Distillery Hand Sanitizer Recalled for Misleading Beverage-Like Packaging
Prairie Wolf Distillery Alcohol Antiseptic 80% hand sanitizer is being recalled because the bottles resemble beverage containers, creating a risk of accidental ingestion. The recall affects all lots of both the 500 mL and 591 mL sizes distributed nationwide.
Product
Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer, packaged in a) (16.9oz) 500 mL (UPC 8 60003 31899 7, NDC: 73891-100-14); and b) (20oz) 591 mL (UPC 8 60003 65984 7 NDC: 73891-100-15) bottles, Prairie Wolf Distillery, Guthrie, Oklahoma
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0656-2021·2021-07-21
Durisan Antimicrobial Hand Sanitizer recalled for microbial contamination
Sanit Technologies is recalling Durisan Antimicrobial Solutions hand sanitizer due to internal testing that found contamination with Burkholderia contaminans and/or yeast and mold in certain lots.
Product
Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizer, listed as 0.1% or 0.13%, Alcohol-Free, packaged in a) 18 mL Net Content 0.61 fl oz credit card size container, (UPC 8 52379 00614 1); b) 50 mL Net Content 1.69 oz bottle, (UPC 8 52379 00634 9 and 8 52379 0061
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0691-2021·2021-07-21
Limar Hand Sanitizer recalled for deceptive container packaging
Limar Hand Sanitizer (70% isopropyl alcohol) in 4 oz bottles is being recalled because the containers resemble drinking water bottles, creating a risk of accidental ingestion.
Product
Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont. 4 oz bottles, Manufactured in Dominican Republic: by Ardil Comercial S.R.L., Santo Domingo, Dominican Republic UPC 7 487040 301587
Category
Drug
Distribution
0 states

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5126–5150 of 17964