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

6576–6600 of 89512

CriticalFDA (Devices)·Z-1946-2025·2025-06-25
Dexcom One Continuous Glucose Monitoring System Receiver Speaker Defect
Dexcom, Inc. is recalling Dexcom One Continuous Glucose Monitoring System receivers due to potential defective foam or assembly errors that may cause the speaker to lose contact with internal components, resulting in missed audible alerts for dangerous blood glucose levels.
Product
Dexcom One Continuous Glucose Monitoring System, SKUs(Part Number): STK-DO-006 (MT27409-1), STK-DO-013 (MT27409-1), STK-DO-103 (MT27409-2), STK-DO-109 (MT27409-2)
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1944-2025·2025-06-25
Dexcom G7 Glucose Receiver recalled due to defective foam or assembly error
Dexcom, Inc. is recalling Dexcom G7 Glucose Receiver units due to defective foam or assembly error that may cause the speaker to lose contact with the circuit board, preventing audible alerts for low or high blood glucose.
Product
Dexcom G7 Glucose Receiver, SKUs (part number): STK-AT-011(MT26403-0), STK-AT-012 (MT26403-0), STK-AT-013 (MT26403-0), STK-GT-001 (MT26403-1), STK-GT-008 (MT26403-5), STK-GT-013 (MT26403-1) , STK-GT-019 (MT26403-4) , STK-GT-100 (MT26403-2), STK-GT-109 (MT26403-2) , STK-GT-113 (
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0054-2025·2025-06-25
Ready-to-eat salads recalled for potential Salmonella contamination
GBC Food Services is recalling multiple ready-to-eat salad products due to potential Salmonella contamination. The affected salads were purchased between May 8 and May 21, 2025.
Product
Chef Salad 11oz 850065403328 Purchase Dates: 05/08/2025 to 05/21/2025 Family Cobb Salad 22OZ 850054894625 Purchase Dates: 05/08/2025 to 05/21/2025 Individual Garden Salad 12OZ 850054894618 Purchase Dates: 05/08/2025 to 05/21/2025 Individual Greek Salad 12OZ 850054894649 Purchase
Category
Food
Distribution
9 states
SevereFDA (Food)·H-0057-2025·2025-06-25
Ginger Beer Juice Soda Recalled for Potential Salmonella Contamination
RGB Soda, LLC is recalling Refrigerated Cucumber X Tarragon Ginger Beer distributed in Washington due to potential Salmonella contamination. The affected batches were produced on 11/4/2024 and 11/25/2024.
Product
Refrigerated Cucumber X Tarragon Ginger Beer (ginger juice). Product is juice soda and distributed in 5gal. pony keg. The kegs were distributed to the firm's own stores where they were served to glasses. The kegs were labeled with the name of the product and the day it was made.
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-1943-2025·2025-06-25
Dexcom G6 Glucose Receiver recalled for missed audible alerts
Dexcom G6 Glucose Receiver units may have defective foam or assembly errors that disable audible alerts for dangerously low or high blood glucose, risking seizures, loss of consciousness, or death.
Product
Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0493-2025·2025-06-25
UMOVY ACIDO HIALURONICO supplement recalled for undeclared prescription drugs
UMOVY ACIDO HIALURONICO dietary supplement has been recalled because it contains undeclared prescription ingredients Dexamethasone and Diclofenac. The product was marketed without FDA approval.
Product
UMOVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7503046054134
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25V433000·2025-06-25
Chevrolet Blazer EV parking brake wiring can trigger or lose the brake
General Motors is recalling certain 2024-2025 Chevrolet Blazer EV vehicles because a damaged or corroded rear parking brake harness can activate the parking brake while driving, or disable it while parked.
Product
CHEVROLET — CHEVROLET BLAZER EV
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·021-2025-EXP·2025-06-25
Starway Recalls Ineligible Frozen Siluriformes Fish Products Imported from Vietnam
Starway International Group is expanding a recall for frozen fish products from an ineligible Vietnamese establishment. No adverse reactions have been reported.
Product
Starway International Group LLC Expands Recall for Ineligible Frozen Siluriformes Fish Products Imported from Vietnam
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V414000·2025-06-25
International CV brake pressure sensor can leak fluid causing fire
International is recalling certain 2019-2025 CV vehicles because the brake pressure sensor assembly may leak brake fluid into the pressure switch and short circuit. Owners are advised to park outside until repaired.
Product
INTERNATIONAL — INTERNATIONAL CV
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-0056-2025·2025-06-25
Cucumber Carrot Ranch Pack 20oz recalled for Salmonella contamination
GBC Food Services is recalling Cucumber Carrot Ranch Pack 20oz due to potential Salmonella contamination. The affected products were purchased between May 8 and May 21, 2025, and distributed across nine states.
Product
Cucumber Carrot Ranch Pack 20oz 850065403557 Purchase Dates: 05/08/2025 to 05/21/2025
Category
Food
Distribution
9 states
SevereFDA (Food)·H-0046-2025·2025-06-25
Lancaster LF Authentic Greek Salad Kit Recalled for Salmonella Risk
Reser's Fine Foods is recalling Lancaster LF Authentic Greek Salad Kits distributed in MA and PA because the cucumbers may be contaminated with Salmonella. The kits are implicated in an ongoing Salmonella outbreak.
Product
Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages, net wt. 14.25lb., Item Code 407079, UPC 13454.38482. This is wholesale kit consisting of pre-packaged components in a corrugated box for assembly by retail delis. Kit contains sealed bags of cut produce (sliced cucum
Category
Food
Distribution
2 states
SevereFDA (Drugs)·D-0492-2025·2025-06-25
UNAVY ACIDO HIALURONICO supplement recalled for undeclared pharmaceutical ingredients
UNAVY ACIDO HIALURONICO hyaluronic acid supplement is being recalled because it contains three undeclared pharmaceutical ingredients: Dexamethasone, Diclofenac, and Omeprazole. The product was marketed without FDA approval and poses health risks from the unlisted drugs.
Product
UNAVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7 503046 054295
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0052-2025·2025-06-25
Cucumber bowls and snack cups recalled due to Salmonella contamination risk
GBC Food Services, LLC is recalling cucumber products sold between May 8 and May 21, 2025, due to potential Salmonella contamination. Affected products include Cucumber Bowl with Ranch dip, Cucumber Slices with Tajin, and Cucumber with Ranch Snack Cup.
Product
Cucumber Bowl with Ranch dip 15oz UPC 850054894519 Purchase Dates: 05/08/2025 to 05/21/2025 Cucumber Slices W/Tajin 10 oz UPC 85005368569 Purchase Dates: 05/08/2025 to 05/21/2025 Cucumber w/ Ranch Snack Cup 9.5 oz UPC 850065403144 Purchase Dates: 05/08/2025 to 05
Category
Food
Distribution
9 states
SevereFDA (Food)·F-0938-2025·2025-06-25
Afghani Corn Bread Doda Recalled for Undeclared Wheat and Sesame
Ariana Sweets Inc. is recalling Afghani Corn Bread "Doda" because the product contains undeclared wheat and sesame allergens, which are not listed on the label.
Product
AFGHANI CORN BREAD "Doda"; INGREDIENTS: Corn Flour, Sugar, Vegetable Oil, Eggs, Milk, Black Seeds, Caardamom; ALLERGEN STATEMENT: This product contains eggs, milk, and may contain traces of nuts. NET WT 24.0 oz (680g); Keep Cool. Reheat in oven if desired.
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-1902-2025·2025-06-25
Cook Beacon Tip Angiographic Catheters Recalled for Tip Separation Risk
Cook Incorporated is recalling specific lots of Beacon Tip 5.0 Fr Angiographic catheters due to the risk that the catheter tip may separate during use. The affected catheters were distributed worldwide.
Product
Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters are available in various configurations. Configurations include different shaft lengths and tip curves and some catheters are manufactured with a hydrophilic coati
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·H-0053-2025·2025-06-25
Vegetable Bowls and Trays Recalled for Potential Salmonella Contamination
GBC Food Services is recalling vegetable bowls and vegetable ranch trays due to potential Salmonella contamination. Affected products were purchased between May 8 and May 21, 2025.
Product
Vegetable Bowl $5 13oz 850065403380 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Bowl $10 26 oz 860010507131 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Ranch Tray No Dip Small 19.50 oz 850054894335 Purchase Dates: 05/08/2025 to 05/21/2025 Large Vegetable Tray
Category
Food
Distribution
9 states
HighFDA (Devices)·Z-1992-2025·2025-06-25
Fresenius 5008X HDF Hemodialysis Blood Tubing Sets recalled for potential blood leaks
Fresenius Medical Care is recalling 5008X HDF Hemodialysis Blood Tubing Sets due to potential blood leaks between the venous chamber and tubing. The recall affects hemodialysis, hemodiafiltration, hemofiltration, and isolated ultrafiltration procedures nationwide.
Product
5008X HDF Hemodialysis Blood Tubing Set, 24 units per case, with the following models: a. 5008X Standard HDF Bloodline, Model Number: 03-5100-7. b. 5008X Standard HDF Bloodline w/CLIC, Model Number: 03-5100-7C. c. 5008X Standard HDF Bloodline w/ Twister, Model Number: 03-5150-
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1981-2025·2025-06-25
UROSKOP Omnia X-ray System Model 10094910 Frequency Inverter Overheating Recall
Siemens is recalling 95 units of the UROSKOP Omnia X-ray system nationwide due to a resistor in the frequency inverter that may overheat and potentially ignite the plastic housing.
Product
UROSKOP Omnia. Model Number: 10094910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1989-2025·2025-06-25
Prestige Coil System implantable devices recalled for manufacturing defect
BALT USA is recalling Prestige Coil System implantable embolization devices because radiopaque markers on some units were not manufactured to specification and were not visible during angiography.
Product
Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 00810068567663 PRES1245CPKPLT 00810068567694 PRES1445CPKPLT 00810068567724 PRES0103CXPPLT 00810068567304 PRES2512CXPPLT 00810068567397 PRES0258CXPPLT 00810068567380 PRES0212CXPPLT 0081006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0047-2025·2025-06-25
Pain Train Salsa Creamy Avocado Spicy Recalled for Undeclared Milk
Pain Train Salsa - Creamy Avocado Spicy (12 oz, refrigerated) is recalled due to undeclared milk allergen. The product was distributed in Texas.
Product
Pain Train Salsa - Creamy Avocado Spicy Refrigerated. Shelf Life 90 days. 12 oz Flexible Plastic containers. UPC: 19589339802
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1988-2025·2025-06-25
Optima Coil System embolization coils recalled for defective radiopaque marker
BALT USA is recalling the Optima Coil System because the radiopaque marker was not visible during angiography and was not manufactured to specification.
Product
Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851 OPTI0258BLK 00810068568929 OPTI0212BLK 00810068568912 OPTI0206BLK 00810068568905 OPTI0310BLK 00810068568943 OPTI0320BLK 00810068568950 OPTI0151HSS10 008
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0050-2025·2025-06-25
Great Plains Bentonite Herbal Detox Capsules Recall
Yerba Prima Inc is recalling Great Plains Bentonite + Herbal Detox Capsules due to potential contamination with Pseudomonas aeruginosa. Affected bottles have Lot # 05051 with expiration date 02/2028.
Product
Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper proof seal. Case GTIN code:100 46352 00518 5. Retail package UPC code: 0 46352 00518 8. Yerba Prima, Inc. 740 Jefferson Ave Ashland, Oregon 97520 USA
Category
Food
Distribution
21 states
HighFDA (Food)·H-0055-2025·2025-06-25
Fruit and Veg Tray 64oz Recalled for Potential Salmonella Contamination
GBC Food Services, LLC is recalling Fruit and Veg Tray 64oz products due to potential Salmonella contamination. The affected products were distributed to multiple states and purchased between May 8 and May 21, 2025.
Product
Fruit and Veg Tray 64oz 850065403748 Purchase Dates: 05/08/2025 to 05/21/2025
Category
Food
Distribution
9 states
HighFDA (Devices)·Z-1980-2025·2025-06-25
Portable Oxygen Concentrator with Erroneous Calibration Values
Ohio Medical Corporation is recalling 36 units of the GCE HEALTHCARE Zen-O lite portable oxygen concentrator due to erroneous calibration values that may cause the device's alarm for low oxygen purity to function incorrectly as the device ages.
Product
GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1982-2025·2025-06-25
Siemens UROSKOP Omnia Max frequency inverter fire risk recalled
Siemens is recalling UROSKOP Omnia Max medical devices due to a resistor in the frequency inverter that may overheat and ignite the plastic housing. Twenty-five units distributed nationwide are affected.
Product
UROSKOP Omnia Max. Model Number: 10762473
Category
Medical Device
Distribution
Distributed nationwide

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6576–6600 of 89512