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

6626–6650 of 7514

SevereFDA (Drugs)·D-0395-2022·2022-02-02
Lidocaine HCl Sterile Buffered Solution Recalled for Lack of Sterility Assurance
Edge Pharma is recalling Lidocaine HCl Sterile Buffered Solution for Injection (1%, 10 mL syringes) due to lack of assurance of sterility. The recall affects approximately 4,465 syringes distributed nationwide.
Product
Lidocaine HCl Sterile Buffered Solution for Injection (PF) 1%, 10mL per syringe, Single Use Syringe for Infiltration and Nerve Block, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-0850-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0592-2022·2022-02-02
Fresh Express Romaine Chopped Salad Recalled for Listeria Risk
Fresh Express Inc is recalling Romaine Chopped salad in 32oz. and 2lb. packages due to potential Listeria monocytogenes contamination. The recall affects approximately 9,741 cases distributed across 20 U.S. states and Canada.
Product
"Romaine Chopped" (salad product) packed in 32oz. and 2lb. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0532-2022·2022-02-02
Fresh Express Bacon Thousand Island Salad Recalled for Listeria Risk
Fresh Express Inc is recalling Bacon Thousand Island salad in 9.4 oz packages due to potential Listeria monocytogenes contamination. The recall affects 9,116 cases distributed across multiple U.S. states and Canada.
Product
"Bacon Thousand Island" (salad product) packed in 9.4oz. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0539-2022·2022-02-02
Fresh Express "Chopped Asian" Salad Recalled for Listeria Risk
Fresh Express Inc is recalling "Chopped Asian" salad products in multiple package sizes due to potential Listeria monocytogenes contamination. The products were distributed to domestic and Canadian retailers.
Product
"Chopped Asian" (salad product) packed in 12oz., 12.3oz., and 13.6oz. packages
Category
Food
Distribution
20 states
SevereFDA (Drugs)·D-0412-2022·2022-02-02
MVASI Sterile Ophthalmic Solution Lacks Assured Sterility
Edge Pharma is recalling MVASI (bevacizumab-awwb) intraocular injection syringes nationwide due to lack of assurance of sterility. The recall affects 199 syringes with code 11-2021-01@2 dated 12/15/2021.
Product
MVASI, (bevacizumab-awwb), Sterile Ophthalmic Solution for Injection, 3.25mg/0.13mL (25 mg/mL) 0.13 mL per syringe, Dose: 1.25mg/0.05mL, Single Use Syringe For Intraocular Injection, Edge Pharma, LLC, 856 Hercules Dr. Colchester, VT 05446, NDC 05446-1661-13
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0408-2022·2022-02-02
Mitomycin-C Sterile Ophthalmic Solution Lacks Sterility Assurance
Edge Pharma is recalling Mitomycin-C Sterile Ophthalmic Solution because the manufacturer cannot assure that the product is sterile. The recall affects 163 syringes distributed nationwide.
Product
Mitomycin-C Sterile Ophthalmic Solution, Preservative Free, 0.32mg/0.8 mL (0.4mg/mL) 0.8 mL per syringe, Single Use Syringe, For Topical Ophthalmic Use, Edge Pharma LLC, 856 Hercules Dr. Colchester, VT 05446, NDC 05446-1009-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0493-2022·2022-02-02
Trilogy Evo Ventilator Recalled for Foam Degradation Risk
Philips Respironics recalls 473 Trilogy Evo ventilators due to non-conforming foam that may degrade and release particles. Affected patients risk inhaling or ingesting foam particles and chemicals during device use.
Product
Trilogy Evo, Material Numbers DS2110X11B (USA) and KR2110X15B (Korea) The Trilogy Evo ventilator provides continuous or intermittent positive pressure ventilation for the care of individuals who require mechanical ventilation. Trilogy Evo is intended for pediatric through adul
Category
Medical Device
Distribution
17 states
SevereFDA (Drugs)·D-0401-2022·2022-02-02
Edge Pharma Edetate Disodium Ophthalmic Solution Recall for Sterility Concerns
Edge Pharma is recalling Edetate Disodium (EDTA) 3% Sterile Ophthalmic Solution due to lack of assurance of sterility. The product is a single-dose eye drop used for topical ophthalmic use.
Product
Edetate Disodium (EDTA), Sterile Ophthalmic Solution, (PF) 3%, 10mL per dropper, Single Dose Droptainer for Topical Ophthalmic Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT, 05446, NDC 05446-1428-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0595-2022·2022-02-02
Fresh Express Shredded Lettuce Recall Due to Listeria Contamination Risk
Fresh Express Inc is recalling shredded lettuce products in multiple package sizes due to potential Listeria monocytogenes contamination. The recall affects approximately 211,228 cases distributed across 20 U.S. states and Canada.
Product
"Shredded Lettuce" (salad product) packed in 8oz., 14oz., 16oz., and 5lb. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0594-2022·2022-02-02
Santa Fe Bowl salad product recalled for potential Listeria contamination
Fresh Express Inc is recalling Santa Fe Bowl salad in 5.23oz and 5.7oz packages due to potential Listeria monocytogenes contamination. The product was distributed to over 100 U.S. distributors and Canada.
Product
"Santa Fe Bowl" (salad product) packed in 5.23oz. and 5.7oz. packages
Category
Food
Distribution
20 states
SevereFDA (Drugs)·D-0424-2022·2022-02-02
Vancomycin HCl Ophthalmic Solution Recalled for Sterility Assurance
Edge Pharma LLC is recalling Vancomycin HCl sterile ophthalmic solution for injection due to lack of assurance of sterility. The affected product was distributed nationwide.
Product
Vancomycin HCl, Sterile Ophthalmic Solution for Injection, Preservative Free, 8 mg/0.8mL (10 mg/mL) (vancomycin equivalent), 0.8 mL per syringe, Single Use Syringe, For Intraocular Injection, Edge Pharma LLC, 856 Hercules Dr., Colchester, VT, 05446, NDC 05446-0736-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0610-2022·2022-02-02
Twisted Chopped Greek Caesar Salad Recalled for Listeria Risk
Fresh Express Inc is recalling Twisted Chopped Greek Caesar salad in 9.3oz packages due to potential Listeria monocytogenes contamination. The product was distributed to retailers in 20 U.S. states and Canada.
Product
"Twisted Chopped Greek Caesar" (salad product) packed in 9.3oz. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0566-2022·2022-02-02
Fresh Express Kale Caesar Salad Recalled for Listeria Contamination Risk
Fresh Express Inc is recalling Kale Caesar salad in 8.5oz packages due to potential Listeria monocytogenes contamination. Affected products were distributed across 23 US states and Canada.
Product
"Kale Caesar" (salad product) packed in 8.5oz. packages
Category
Food
Distribution
20 states
SevereFDA (Devices)·Z-0494-2022·2022-02-02
Trilogy Evo Ventilator Repair Kit Recalled for Degrading Foam Material
Philips Respironics recalled 205 Trilogy Evo ventilator repair kits containing non-conforming foam material that may degrade into particles potentially inhaled or ingested by users. The affected kits were distributed in the US and internationally.
Product
Trilogy Evo Repair Kit, RP-Trilogy Evo Muffler Assembly, Material Number 1135257 The Trilogy Evo ventilator provides continuous or intermittent positive pressure ventilation for the care of individuals who require mechanical ventilation. Trilogy Evo is intended for pediatric t
Category
Medical Device
Distribution
17 states
CriticalFDA (Devices)·Z-0450-2022·2022-01-26
Medtronic HawkOne Atherectomy System Recalled for Tip Detachment and Embolization Risk
Medtronic is recalling the HawkOne Directional Atherectomy System globally due to reports of tip damage that can detach and cause embolization. The device is used to remove arterial plaque in peripheral blood vessels.
Product
Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-M and H1-M-INT., Multi-vessel, 6F (2.2 mm) Recommended sheath, 0.014" (0.36 mm) Compatible guidewire. The HawkOne directional atherectomy system is intended for use in atherectomy of the peripheral vasculature
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0451-2022·2022-01-26
Medtronic HawkOne Directional Atherectomy Device Recalled for Tip Damage
Medtronic is recalling 28,094 units of its HawkOne directional atherectomy system due to reports of catheter tip damage and detachment that can cause blood clots in blood vessels.
Product
Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-S and H1-S-INT, Small Vessel, 6F (2.2 mm) Recommended sheath, 0.014" (0.36 mm) Compatible guidewire. The HawkOne directional atherectomy system is intended for use in atherectomy of the peripheral vasculature.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0505-2022·2022-01-26
Haifa Smoked Turbot Fish Recalled for Listeria Contamination
D & M Smoked Fish, Inc. is recalling Haifa Smoked Turbot Cold Smoked (8 oz) because it may be contaminated with Listeria monocytogenes. The product was distributed in New York and New Jersey.
Product
"Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z."
Category
Food
Distribution
2 states
SevereFDA (Drugs)·D-0462-2022·2022-01-26
Semglee Insulin Glargine Prefilled Pens Missing Label
Mylan Pharmaceuticals is recalling approximately 73,175 Semglee (insulin glargine) prefilled pens nationwide because some units have a missing label. Patients should check their pens and contact their pharmacist or doctor if affected.
Product
Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL Prefilled Pen (NDC 49502-0196-71), packaged in Five 3 mL Prefilled Pens per carton (NDC 49502-0196-75), Rx only, Manufactured in Malaysia for: Mylan Specialty L.P., Morgantown, WV, 26505.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0377-2022·2022-01-26
SENNA Syrup unit-dose cups recalled for microbial contamination
Lohxa, LLC is recalling SENNA Syrup (sennosides) 8.8 mg/5 mL unit-dose cups due to microbial contamination of the non-sterile product. The recall affects Lot #AM1115S with expiration date 01/2023, distributed nationwide.
Product
SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC 50262-731-24.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0456-2022·2022-01-19
Health Naturals Live Oak Nootropic Mind Capsules Recalled for Undeclared Milk
NutraCap Labs LLC is recalling Health Naturals/Live Oak Nootropic Mind Capsules 90ct bottles because they contain undeclared milk. The product was distributed across 25 U.S. states.
Product
Health Naturals/ Live Oak Nootropic Mind Capsules 90ct Bottle UPC CODE 7 48528 53969 4
Category
Food
Distribution
26 states
SevereFDA (Food)·F-0445-2022·2022-01-19
Grow Young Fitness Joint Support Capsules recalled for undeclared shellfish
NutraCap Labs LLC is recalling Grow Young Fitness Movin' Joint Support Capsules because the product contains undeclared shellfish, which poses a risk to consumers with shellfish allergies.
Product
Grow Young Fitness Movin' Joint Support Capsules 150ct UPC CODE 6 96550 08806 5
Category
Food
Distribution
26 states
SevereFDA (Food)·F-0519-2022·2022-01-19
Moor Herbs Infant Formula Recall: Unsafe Mineral Levels and Missing Vitamin D
Moor Herbs Healthy Beauty Angel Formula, marketed as an infant formula, has not undergone required FDA pre-market notification. The product contains excessive iron, potassium, and sodium, and lacks vitamin D, posing risks to infants.
Product
Moor Herbs Healthy Beauty Angel Formula packed in 16oz. plastic containers
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0450-2022·2022-01-19
NutraCap Labs Candy Bliss Recalled for Undeclared Milk
NutraCap Labs LLC is recalling Human Performance Synapse Candy Bliss 16oz jars (Lot #2002005, expiration 02/2022) because the product contains undeclared milk, which poses a risk to consumers with milk allergies.
Product
Human Performance Synapse Candy Bliss 16oz Jar NO UPC CODE
Category
Food
Distribution
26 states
SevereFDA (Food)·F-0463-2022·2022-01-19
Muscle Rage King Test Capsules Recalled for Undeclared Milk
NutraCap Labs LLC is recalling Muscle Rage King Test Capsules (300ct, UPC 5 06055 94301 42) because the product contains undeclared milk. This poses a risk to consumers with milk allergies.
Product
Muscle Rage King Test Capsules 300ct Bottle UPC CODE 5 06055 94301 42
Category
Food
Distribution
26 states
SevereFDA (Food)·F-0469-2022·2022-01-19
New Alpha Nutrition Huge Load Capsules Recalled for Undeclared Milk
NutraCap Labs LLC is recalling New Alpha Nutrition Huge Load Capsules (90ct bottles) due to undeclared milk. The product poses a risk to consumers with milk allergies.
Product
New Alpha Nutrition Huge Load Capsules 90ct Bottle NO UPC CODE
Category
Food
Distribution
26 states

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6626–6650 of 7514