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

6876–6900 of 89525

HighFDA (Food)·F-0928-2025·2025-06-11
GNC Women's 30+ Vitapak recalled due to undeclared fish allergen
GNC Holdings LLC is recalling GNC Women's 30+ Vitapak due to undeclared fish allergen (parvalbumin). The product was distributed across multiple states.
Product
GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that measures 10.25 width x 3.56 height x 3.15 depth containing 30 sachets of 3 width x 2.75 height with tear notch. 15 Cartons per Case
Category
Food
Distribution
48 states
HighFDA (Food)·F-0823-2025·2025-06-11
Artisan Multigrain Bread recalled for undeclared egg allergen
NEW GRAINS GLUTEN FREE BAKERY is recalling Artisan Multigrain Bread (32 oz packages) distributed in Utah because label printing quality failed to clearly declare the egg allergen present in the product.
Product
Artisan Multigrain Bread: Gluten-free multigrain bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Honey, Golden flax seed, Palm oil, Potato flour, Yeast, Sugar, Psyllium husk powder, Rice bran, Sea salt,
Category
Food
Distribution
1 state
HighFDA (Food)·F-0838-2025·2025-06-11
Pecan Caramel Bars Recalled for Undeclared Allergen Labels
New Grains Gluten Free Bakery is recalling Pecan Caramel Bars sold in Utah because printing quality issues made allergen declarations for egg, milk, and pecans unreadable or missing on the package.
Product
Pecan Caramel Bars Individually wrapped in plastic. Ingredients: White rice flour, Sugar, Honey, Pecan pieces, Butter, Eggs, Rice milk, Potato flour, Vanilla, Baking powder, Xanthan gum, Unflavored gelatin, Sea salt Contains: Egg, Milk, Tree nuts
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1900-2025·2025-06-11
Signature Laparoscopic Atraumatic Grasper Insulation Defect Recall
Silex Medical is recalling Signature Laparoscopic Instruments (Model 5881033) because insulation on the shaft does not fully extend to the proximal end, leaving an exposed area near the rotator wheel.
Product
Signature Laparoscopic Instruments, 20mm Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5881033.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1886-2025·2025-06-11
Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack Recalled
Mozarc Medical is recalling Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Packs due to a potential breach of sterile barrier packaging that could compromise the catheter's sterility.
Product
Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1893-2025·2025-06-11
Signature Laparoscopic Dolphin Nose Grasper Instrument Insulation Defect
Silex Medical is recalling 2 units of a Signature Laparoscopic Instruments Dolphin Nose Grasper with Rotating Shaft due to incomplete insulation on the shaft, leaving an exposed area near the rotator wheel.
Product
Signature Laparoscopic Instruments, Dolphin Nose Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5860020.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V368000·2025-06-11
Nova Bus turn signal indicator lights may remain solidly illuminated
Nova Bus is recalling certain 2022-2023 LFS buses because a digital display firmware error may leave the instrument panel turn signal indicators solidly lit, failing FMVSS 108.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1888-2025·2025-06-11
Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack recalled
Mozarc Medical is recalling Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. The affected catheter models were distributed nationwide in the US and in Canada and Mexico.
Product
Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1908-2025·2025-06-11
Beckman Coulter Sample Probes with Defective Tips Clinical Chemistry
Beckman Coulter is recalling sample probes with defective tips used in clinical chemistry analyzers. The defective probes may dispense lower sample concentrations, potentially leading to false low test results and delayed diagnosis.
Product
Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1896-2025·2025-06-11
Signature Laparoscopic Sharp Tooth Grasper Insulation Defect Recall
Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.
Product
Signature Laparoscopic Instruments, Sharp Tooth Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863020.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1885-2025·2025-06-11
Palindrome Precision Chronic Hemodialysis Catheter Sport Pack Recalled
Mozarc Medical US LLC is recalling Palindrome Precision Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. Affected units were distributed worldwide including the US, Canada, and Mexico.
Product
Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1901-2025·2025-06-11
Access Testosterone assay Catalog Number 33560 recalled
Beckman Coulter is recalling the Access Testosterone assay (Catalog Number 33560) due to inadequate maintenance on manufacturing equipment that caused cross-contamination in testosterone reagent packs, which could result in inaccurate patient test results.
Product
Access Testosterone assay, Catalog Number 33560
Category
Medical Device
Distribution
1 state
HighFDA (Drugs)·D-0455-2025·2025-06-11
Fluoxetine Tablets USP 20 mg Recalled for N-Nitroso Contamination
Torrent Pharma Inc. is recalling Fluoxetine Tablets USP 20 mg due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit. The affected lot is distributed nationwide.
Product
FLUOXETINE — FLUOXETINE (FLUOXETINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0008-2025·2025-06-11
Bengal King Family Pack Vegetable Singara Contains Undeclared Peanut
South Asian Food Inc. is recalling Bengal King Family Pack Vegetable Singara due to undeclared peanut, a major allergen that poses a serious risk to consumers with peanut allergies.
Product
Bengal King Family Pack Vegetable Singara
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1903-2025·2025-06-11
Luminex VERIGENE Gram Negative Blood Culture Test Recalled
Luminex is recalling VERIGENE Gram Negative Blood Culture test cartridges due to a consumable issue that may produce incorrect results on a small portion of one lot.
Product
VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results VERIGENE System; invitro diagnostic test
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0002-2025·2025-06-11
Bedner Growers cucumbers recalled for potential Salmonella contamination
Bedner Growers, Inc. is recalling cucumbers shipped from May 3–12, 2025, due to potential Salmonella contamination. Affected products were distributed in Florida in cardboard boxes of 24, 36, or 68 count.
Product
Cucumbers, Wholesale Produce Supply, Bedner Growers, Inc. 10066 Lee Road Boynton Beach, FL 33473 (561)733-5490. Cucumbers were packaged in cardboard shipping boxes to customers with packaging sizes consisting of 68, 36, or 24 count per box.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1895-2025·2025-06-11
Signature Laparoscopic Debakey Grasper Instruments Recalled for Insulation Defect
Silex Medical is recalling 8 units of Signature Laparoscopic Debakey Grasper instruments (Model 5862100) due to incomplete insulation on the shaft near the rotator wheel, which could expose the user or patient to electrical contact.
Product
Signature Laparoscopic Instruments, Debakey Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862100.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0837-2025·2025-06-11
Dye-Free Frosted Sugar Cookies Recalled for Undeclared Allergens
New Grains Gluten Free Bakery is recalling Dye-Free Frosted Sugar Cookies due to printing quality issues that failed to clearly declare allergens (egg, milk, soy) on the label. The product was distributed in Utah.
Product
Dye-Free Frosted Sugar Cookie: Gluten-free dye-free frosted sugar cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: White rice flour, Powdered sugar, Butter, Sugar, Palm shortening, Sprinkles, Rice milk, Egg whites, Potato flour, Imitation vanilla, Baking powder,
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1889-2025·2025-06-11
MAHURKAR Chronic Hemodialysis Catheter recalled for sterile barrier defect
Mozarc Medical is recalling MAHURKAR Chronic Hemodialysis Catheter Sport Pack units due to a potential breach in sterile barrier packaging that could compromise the product's sterility.
Product
MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0824-2025·2025-06-11
Gluten-Free Artisan White Bread Recall Due to Undeclared Egg Allergen
New Grains Gluten Free Bakery is recalling approximately 41 units of Artisan White Bread due to undeclared egg allergen on the label. Poor print quality rendered the egg allergen declaration illegible or missing.
Product
Artisan White Bread: Gluten-free artisan white bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm oil, Potato flour, Yeast, Rice bran, Psyllium husk powder, Sea salt, Xanthan gum. Contains: Egg.
Category
Food
Distribution
1 state
HighFDA (Food)·H-0001-2025·2025-06-11
Salsa Cilantro recalled for potential foreign object contamination
Mexquisite, Inc. is recalling Salsa Cilantro in 8.5lb plastic jugs due to potential foreign object contamination. The product was distributed to Texas and California.
Product
Salsa Cilantro 8.5lb plastic jugs packaged 4 jugs to case. MSC12114
Category
Food
Distribution
2 states
HighFDA (Food)·F-0927-2025·2025-06-11
Diced Almonds Recalled for Undeclared Milk Allergen
Rocky Mountain Chocolate Factory is recalling diced almonds due to an undeclared milk allergen. Consumers with milk allergies should not consume the product.
Product
Nuts, Almonds DR Diced, LB. Diced Almonds. Bulk (Plastic bag inside corrugated box) Net Wt: 18.5lbs. UPC: 660-1300203. Firm Name & Address Listed on Label: RMCF 265 Turner Dr, Durango CO 81303.
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1897-2025·2025-06-11
Signature Laparoscopic Bullet Tip Grasper Instrument Insulation Defect Recall
Silex Medical is recalling 6 units of the Signature Laparoscopic Bullet Tip Grasper with Rotating Shaft due to incomplete insulation on the shaft near the rotator wheel, which could expose users to electrical hazards.
Product
Signature Laparoscopic Instruments, Bullet Tip Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863030.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0007-2025·2025-06-11
Eudos Bronquilan Recalled for Undeclared Food Color Additives
Nature's Eudos Distributors LLC is recalling Eudos Bronquilan due to undeclared food color additives (FD&C Yellow #5, FD&C Blue #1, and FD&C Red #40). Consumers with allergies or sensitivities to these dyes should not use the product.
Product
Eudos Bronquilan
Category
Food
Distribution
2 states
HighFDA (Food)·H-0011-2025·2025-06-11
Giant Instant Oatmeal Raisins and Spice Recalled for Undeclared Walnuts
Giant Instant Oatmeal Raisins and Spice is being recalled because walnuts are not declared on the outer packaging, though they appear on the inner packaging. Consumers with walnut allergies who rely on outer-package labeling are at risk.
Product
Giant, Instant Oatmeal Raisins and Spice, 10 -1.5 oz. Packets, per box. Net. Wt. 15.01 oz.
Category
Food
Distribution
5 states

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6876–6900 of 89525