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

7326–7350 of 7514

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-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-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-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-0667-2021·2021-07-28
SS Coconut Breeze Scented Sanitizer Recalled for Chemical Contamination
SS Coconut Breeze Scented Sanitizer has been recalled due to contamination with methanol, benzene, and acetaldehyde. The 3.38 FL. OZ. bottles were distributed nationwide.
Product
SS Coconut Breeze 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-0683-2021·2021-07-28
Goose Creek Hand Sanitizer Recalled for Methanol and Benzene Contamination
Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer aloe Tropical Daydream spray due to contamination with methanol, benzene, and acetaldehyde. The product was distributed nationwide.
Product
Goose Creek Hand Sanitizer aloe Tropical Daydream, 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 01335 6
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2074-2021·2021-07-28
Philips Respironics V60 Plus Ventilator software defect reduces oxygen delivery to patients
Respironics V60 Plus Ventilators (software versions 3.00 and 3.10) may reduce oxygen flow below clinical settings, risking oxygen desaturation and hypoxemia in mechanically ventilated patients.
Product
Philips Respironics V60 Plus Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an assist ventilator and is intended to augment patient breathing. It is intended for spontaneously breathing individuals who require mechanical ventilation
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2073-2021·2021-07-28
Philips Respironics V60 Ventilator Flow Rate Reduction Safety Defect
Philips Respironics V60 ventilators with High Flow Therapy software versions 3.00 and 3.10 may reduce oxygen delivery below prescribed levels when pressure limits are reached, risking oxygen desaturation.
Product
Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an assist ventilator and is intended to augment patient breathing. It is intended for spontaneously breathing individuals who require mechanical ventilation: pat
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0790-2021·2021-07-28
Circle K Chicken Salad Sandwich Recall Due to Listeria Risk
LSG Sky Chefs is recalling Circle K Chicken Salad Sandwiches because the chicken used is subject to a national recall due to potential Listeria monocytogenes contamination. The recall affects products with best buy dates of 6/7/21 through 7/9/21 distributed in AZ, CA, and NV.
Product
Circle K Chicken Salad Sandwich, 5.9 oz. (167g) clamshell packaging with tamper strip, UPC 815138013996, Manufactured By: LSG Sky Chefs Supply Chain Solutions, Inc. 3555 S. 28th St. Phoenix, AZ. Perishable/Keep Refrigerated.
Category
Food
Distribution
3 states
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-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-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-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-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-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
SevereCPSC·21764·2021-07-22
Bel Furniture Recalls Barrington 5-Drawer Chests for Tip-Over Hazards
Bel Furniture is recalling about 90 Barrington 5-Drawer Chests because the dressers can tip over and trap children if not anchored to the wall. One child has already been injured when a chest tipped over.
Product
Barrington 5-Drawer Chests
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2019-2021·2021-07-21
INTUA CRT-P Pacemakers Recalled Due to Battery Degradation Risk
The INTUA CRT-P pacemakers (1,707 units) may develop high internal battery impedance later in device life, causing system resets and triggering Safety Mode. Therapy continues but device replacement is required.
Product
INTUA CRT-P, Model Numbers: a) V272 b) V273 c) W273
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2015-2021·2021-07-21
Boston Scientific ADVANTIO DR EL Pacemakers Recalled for Battery Malfunction
Boston Scientific is recalling ADVANTIO DR EL dual chamber pacemakers and CRT-Ps due to a latent battery condition that may cause system resets and trigger Safety Mode, requiring device replacement.
Product
ADVANTIO DR EL (pacemaker), Model Numbers: a) J064 b) J067 c) K064 (added 7/15/2021) d) K084 (added 7/15/2021) e) K087 (added 7/15/2021)
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1956-2021·2021-07-21
Philips Respironics Continuous Ventilators Recalled for Foam Degradation Risk
Philips Respironics is recalling approximately 255,810 continuous ventilators because polyurethane foam may degrade into particles that could be inhaled or ingested, or release chemicals.
Product
Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1957-2021·2021-07-21
Philips Respironics BiPAP ventilators recalled for foam degradation and off-gassing
Philips Respironics BiPAP ventilators' polyurethane foam may degrade into particles that could be inhaled or ingested, or off-gas certain chemicals. About 8,047 devices worldwide are affected.
Product
A-Series BiPAP Hybrid A30 (not marketed in US), A-Series BiPAP V30 Auto Continuous Ventilator, Minimum Ventilatory Support, Facility Use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1974-2021·2021-07-21
Philips Respironics ventilators recalled for degrading foam and chemical hazards
Philips Respironics ventilators are recalled because foam components may degrade and release particles and chemicals that patients could inhale.
Product
SystemOne (Q-Series), DreamStation, DreamStation Go, Dorma 400, Dorma 500, REMstar SE Auto Noncontinuous Ventilators The Philips Respironics E30 ventilator is intended to provide invasive and non-invasive ventilatory support for individuals with Respiratory Insufficiency. It
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2017-2021·2021-07-21
VITALIO DR EL Pacemakers Recalled Due to Battery-Related Device Resets
Boston Scientific is recalling VITALIO DR EL pacemakers with Extended Life batteries due to a latent battery condition that may cause unexpected device resets and Safety Mode activation later in device life.
Product
VITALIO DR EL (pacemaker), Model Numbers: a) J274 b) J277 c) K274 (added 7/15/2021) d) K277 (added 7/15/2021) e) K284 (added 7/15/2021) f) K287 (added 7/15/2021)
Category
Medical Device
Distribution
0 states
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 (Devices)·Z-1972-2021·2021-07-21
Philips Respironics E30 ventilator foam degradation poses inhalation hazard
Philips Respironics E30 ventilators may have polyurethane foam that degrades into particles. These particles can enter the air pathway and be inhaled or ingested by patients, or the foam may off-gas chemicals.
Product
Philips Respironics E30 with Humidifier, Continuous Ventilator, Minimum Ventilatory Support, Facility Use; Product Numbers DSX9999H11, INX9999H19, RINX9999H19 The Philips Respironics E30 ventilator is intended to provide invasive and non-invasive ventilatory support for indiv
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2018-2021·2021-07-21
Boston Scientific INGENIO CRT-P Pacemakers Recalled for Battery Defect
Boston Scientific is recalling INGENIO CRT-P pacemakers that may develop high internal battery impedance, causing unexpected device resets and Safety Mode activation. Affected devices require replacement.
Product
INVIVE CRT-P, Model Numbers: a) V172 b) V173 c) V182 d) V183 e) W172 f) W173
Category
Medical Device
Distribution
0 states

How to read this listing

Filters

7326–7350 of 7514