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

12401–12425 of 27719

HighFDA (Devices)·Z-1923-2024·2024-06-05
ClearCut and A-OK ophthalmic surgical knives recalled for sharpness issues
Alcon is recalling ClearCut Dual Bevel Sideport and A-OK Corneal/Scleral V-Lance ophthalmic surgical knives due to increased complaint reports about sharpness. Approximately 427,764 units are affected worldwide.
Product
ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1903-2024·2024-06-05
Stryker neurovascular devices recalled for inadequate endotoxin testing
Stryker Neurovascular is recalling Trevo ProVue devices due to manufacturing testing deficiency that may result in unsafe endotoxin levels and risk of fever, shock, or aseptic meningitis.
Product
Trevo ProVue, Catalog: 90184
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1267-2024·2024-06-05
Ganache candy boxes recalled nationwide for undeclared coconut allergen
Maribel's Sweets is recalling 4,011 boxes of 4-piece ganache candy because they contain undeclared coconut, which poses an allergen risk to consumers with coconut allergies.
Product
3. 4pc ganache box
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0517-2024·2024-06-05
Metoprolol Tartrate Tablets Recalled Nationwide for Metal Contamination
Rubicon Research is recalling 11,664 bottles of Metoprolol Tartrate 25mg tablets nationwide due to the presence of metal in the tablets. Consumers should discontinue use and contact their healthcare provider.
Product
METOPROLOL TARTRATE — METOPROLOL TARTRATE (METOPROLOL TARTRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1914-2024·2024-06-05
Stryker Mako Surgical System Software Error Affects Knee and Hip Replacements
Stryker Orthopaedics is recalling Mako surgical system software used for knee and hip replacement procedures due to a software error that causes treatment delays when switching between surgical applications without proper system restart.
Product
Total Knee Arthroplasty (TKA) 2, Total Knee Arthroplasty (TKA) 1, Partial Knee Arthroplasty (PKA) 3, Total Hip Arthroplasty (THA) 4.0, 4.1 on Mako 3.0, 3.1 Software: TKA 2.0.de.1+TKA 1.0.1.de.1+PKA3.0.2.de. Application Part Number: 700002190743-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0530-2024·2024-06-05
ALOE GATOR SPF 40+ Sunscreen Recalled for Out-of-Specification Active Ingredient
ARG Laboratories is recalling ALOE GATOR SPF 40+ sunscreen (4 oz, Lot 04023C1) distributed nationwide due to out-of-specification active ingredient levels that may affect product efficacy.
Product
ALOE GATOR, (Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%), SPF 40+, Broad Spectrum Protective Gel, Sport Performance, NET WT 4 OZ (113g), Manufactured for AGS Brands. UPC 0 17971 10421 7
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1929-2024·2024-06-05
BD Pyxis MedStation ES 7-Drawer Auxiliary Tower Recalled for Fire Risk
CareFusion recalled 87,302 units of the BD Pyxis MedStation ES 7-Drawer Auxiliary Tower due to potential fluid ingress that could cause smoke, system downtime, or fire.
Product
BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower, REF: 324
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0526-2024·2024-06-05
Golden Tiger Pain Relief Cream Recalled for Out-of-Specification Ingredients
ARG Laboratories is recalling Golden Tiger Natural Pain Relieving Cream nationwide due to an active ingredient that does not meet specifications and violative grade propylene glycol used during manufacturing.
Product
NATURAL PAIN RELIEVING CREAM, GOLDEN TIGER, (Camphor 3%, Menthol 3%)Enriched with Pump Capsaicin, Aloe Vera, Willow Bark & MSM, Bottle with Pump NET WT 32 fl. oz (946.33ml), Manufactured for Golden Tiger LLC Made in USA, UPC 1 82294 00004 8
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0521-2024·2024-06-05
Pain Relieving Cream Recalled Due to Out-of-Specification Active Ingredient
ARG Laboratories' Natural Pain Relieving Cream Golden Tiger is being recalled due to out-of-specification active ingredient and improper-grade propylene glycol used in manufacturing. No illnesses have been reported.
Product
NATURAL PAIN RELIEVING CREAM, GOLDEN TIGER, (Camphor 3%, Menthol 3%) Enriched with Capsaicin, Aloe Vera, Willow Bark & MSM, Gallon Jug 128 fl. oz. (3776 ml), Manufactured for Golden Tiger LLC, Made in USA, UPC 1 82294 00005 5
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·23V352000·2024-06-05
Jeep Grand Cherokee Steering Column Intermediate Shaft Defect Recall
Certain 2021–2023 Jeep Grand Cherokee models have an incorrectly assembled steering column intermediate shaft that may disconnect and cause loss of steering control, increasing crash risk. Chrysler is offering free inspection and replacement.
Product
JEEP — 2021 JEEP GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1919-2024·2024-06-05
Dako CoverStainer Microscope Slide Stainer Recalled for Plexiglass Door Breakage
Agilent Technologies recalls Dako CoverStainer microscope slide stainers due to potential plexiglass door breakage that could cause injury.
Product
Brand Name: Dako CoverStainer, Dako CoverStainer CPO Product Name: CoverStainer, CoverStainer CPO Model/Catalog Number: CS10030, CS10040, CS10026, CS10026E Software Version: N/A Product Description: Microscope Slide Stainer IVD Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1898-2024·2024-06-05
Radiographic imaging system tubes may fall due to bolt rupture
FUJIFILM's FDR Visionary Suite radiographic imaging system has bolts that may rupture due to fatigue, potentially causing the tube support to fall and injure patients. The recall affects 18 units distributed across nine states.
Product
FDR Visionary Suite - Intended to generate digital or conventional radiographic images of the skull, spinal column, chest, abdomen, extremities, and other body parts of human anatomies in all routine radiography examinations. Model/Catalog Number: 566-16130-23 566-16130-33
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1924-2024·2024-06-05
Alcon ClearCut S and A-OK ophthalmic surgical knives recalled for sharpness defects
Alcon is recalling about 19,867 ClearCut S and A-OK ophthalmic surgical knives worldwide due to an increase in complaints about blade sharpness.
Product
ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0531-2024·2024-06-05
EYLEA injectable eye medication recalled due to sterility and syringe breakage
Regeneron is recalling 405,725 prefilled syringes of EYLEA (aflibercept) eye injection due to lack of assurance of sterility and complaints of syringe breakage. This FDA Class II recall affects multiple lots distributed nationwide.
Product
EYLEA — EYLEA (AFLIBERCEPT)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1902-2024·2024-06-05
Trevo XP ProVue neurovascular retriever devices recalled for inadequate endotoxin testing
Stryker Neurovascular's Trevo XP ProVue Retriever devices did not undergo adequate endotoxin testing and may exceed safe limits, potentially causing fever, shock, and aseptic meningitis.
Product
Trevo XP ProVue Retriever 4 x 20, Catalog: 90182 Trevo XP ProVue Retriever 3 x 20, Catalog: 90183 Trevo XP ProVue Retriever 4 x 30, Catalog: 90185 Trevo XP ProVue Retriever 6 x 25, Catalog: 90186 Kits: TREVO XP 3X20+PRO14 2-PACK, Catalog: 80051 TREVO XP 4X20+PRO18 2-PACK
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V351000·2024-06-05
Fleetwood, Holiday Rambler Motorhomes Recalled for Damaged Trailer Hitch
REV Recreation Group is recalling 2020-2024 Fleetwood Bounder, Holiday Rambler Vacationer, and select Fleetwood Southwind motorhomes. The trailer hitch may become damaged due to stress or overloading, potentially causing the towed vehicle to separate.
Product
FLEETWOOD — 2020 FLEETWOOD BOUNDER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1932-2024·2024-06-05
BD Pyxis Anesthesia Station 4000 Recalled for Fluid Ingress Fire Risk
CareFusion's BD Pyxis Anesthesia Station 4000 is recalled due to potential fluid ingress that may cause smoke, fire, or system downtime. The recall involves 11,875 units distributed worldwide.
Product
BD Pyxis(TM) Anesthesia Station 4000, REF: 338
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1925-2024·2024-06-05
Ophthalmic surgical knives recalled due to sharpness complaints
Alcon is recalling ClearCut S Safety Sideport Knife (1.2mm Dual Bevel) due to increased reports of sharpness issues. The recall affects 4,930 units distributed worldwide.
Product
ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1906-2024·2024-06-05
Stryker Neurovascular Microcatheter Recall Due to Inadequate Endotoxin Testing
Stryker Neurovascular is recalling the Trevo Trak 21 Microcatheter due to potential endotoxin contamination from inadequate testing. High endotoxin levels may increase risk of fever, shock, and aseptic meningitis.
Product
Trevo Trak 21 Microcatheter, Catalog: 90338
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1281-2024·2024-06-05
H-E-B Chocolate Ice Cream recalled for potential metal contamination
H-E-B Creamy Creations Chocolate Ice Cream 3-ounce 12-packs distributed in Texas are recalled due to potential metal contamination. Consumers should not consume the affected product.
Product
3-ounce H-E-B Creamy Creations Chocolate Ice Cream-12 pk
Category
Food
Distribution
0 states
HighFDA (Food)·F-1280-2024·2024-06-05
H-E-B Ice Cream Recalled for Potential Metal Contamination
H-E-B Creamy Creations ice cream in 12-packs is being recalled due to potential metal contamination. Affected products have code dates from August 31 to September 3, 2024, and were distributed in Texas.
Product
3-ounce H-E-B Creamy Creations Ice Cream Lime/Orange Combo - 12 pack
Category
Food
Distribution
0 states
HighFDA (Drugs)·D-0513-2024·2024-06-05
Intraocular Injection Recalled for Sterility Assurance Failure
Imprimis NJOF, LLC is recalling preservative-free intraocular injection vials of Dexamethasone-Moxifloxacin due to lack of assurance of sterility. Approximately 39,700 vials were distributed nationwide.
Product
Dexamethasone-Moxifloxacin (1 mg/mL and 5mg/mL) Preservative-Free, 1mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-512-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1918-2024·2024-06-05
Medline medical procedure kits recalled for potential needle guide ring detachment
Medline is recalling 12,994 paracervical and pudendal procedure kits because the Trumpet Needle Guide ring can detach when excessive pressure is applied, potentially causing injury.
Product
Medline medical procedure kits, labeled as follows: a) PARACERVICAL PUD TRAY, REF DYNDH1832; b) AHS PARACERVICAL/PUDENDAL KIT, REF DYNJRA2210; c) PARACERVICAL/PUDENDAL BLK KIT, REF DYNJRA9046; d) PARACERVICAL/PUDENDAL BLK KIT, REF DYNJRA9046H; Medical procedure conve
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1900-2024·2024-06-05
EsophaCap Sponge May Detach From String During Removal
Lucid Diagnostics is recalling EsophaCap medical devices (220 units in MN and MD) because the sponge may detach from the string during removal, particularly at esophageal sphincters.
Product
Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) Model/Catalog Number: EC25T10VI Software Version: N/A Product Description: EsophaCap is pouched as individual units. 10 units go into a shelf-box. Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1277-2024·2024-06-05
Texas Pecan Co Mixed Nuts Recalled for Potential Allergen Cross-Contamination
Texas Pecan Co is recalling mixed nut and dried fruit products due to potential cross-contamination with milk, soy, sesame, wheat, tree nuts, and peanuts. Consumers with allergies should not consume the affected products.
Product
1lb and 8oz bags include Apricots, Whole Dates, golden Raisins, Mangos, Currants, Blueberries, Cranberries, Prunes, Raw Sunflower Seeds, Raw Pumpkin Seeds, Pecan Medium Pieces, Blanched Sliced Almonds, Natural Sliced Almonds, Blanched Slivered Almonds, Blanched Whole Almonds and
Category
Food
Distribution
0 states

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12401–12425 of 27719