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

8326–8350 of 31217

HighFDA (Devices)·Z-1382-2025·2025-03-26
Microstream Neonatal-Infant CO2 Filter Line May Be Difficult to Disconnect
Microstream Neonatal-Infant Intubated CO2 Filter Lines may become difficult or impossible to disconnect from endotracheal tubes during clinical procedures, potentially delaying treatment and causing unintended extubation.
Product
Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Infant Intubated, PT00134354 - Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 2m/6.5ft Extended Duration, QMVIIH
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1391-2025·2025-03-26
IsoLoc Prostate Treatment Balloon Devices Recalled for Incorrect Fill Volume Labeling
Angiodynamics is recalling 1,800 units of IsoLoc prostate treatment balloons due to incorrect fill volume labeling. The affected devices were distributed nationwide.
Product
IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit; UPN/Catalog Number: ISO-60;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0288-2025·2025-03-26
Medline Alcohol Prep Pads Recalled for Subpotent Isopropyl Alcohol
Medline Industries has voluntarily recalled over 6.6 million alcohol prep pads nationwide because the product contains less isopropyl alcohol than labeled. The subpotent product was first reported on March 26, 2025.
Product
MEDLINE ALCOHOL PREP — MEDLINE ALCOHOL PREP (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1386-2025·2025-03-26
Access 2 Immunoassay Analyzer motor alignment issue may delay results
Beckman Coulter is recalling Access 2 Immunoassay Analyzers due to sample motor misalignment that may delay patient test result reporting. The recall affects 873 units distributed worldwide.
Product
Access 2 Immunoassay Analyzer, Catalog Number 81600N
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1374-2025·2025-03-26
Modular Stem Orthopedic Implants Recalled for Incorrect GTIN Labeling
Waldemar Link is recalling 20 units of Modular Stem orthopedic implants due to incorrect GTIN labeling on the outer carton. The label bears a barcode for a different product.
Product
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA = 13 mm, Product Code: 880-601/13
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0282-2025·2025-03-26
Ciprofloxacin Ophthalmic Solution Recalled Nationwide for Defective Container Cap
Ciprofloxacin Ophthalmic Solution is being recalled because the cap spike is lodged in the bottle nozzle, preventing patients from accessing the medication. Affected lot 084A067 was distributed nationwide.
Product
CIPROFLOXACIN — CIPROFLOXACIN (CIPROFLOXACIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1373-2025·2025-03-26
Hip Prosthetic Stem Recalled for Incorrect Product Code Label
A modular hip prosthetic stem (52 units) is being recalled due to an incorrect GTIN barcode on the outer carton label, which displays the code for a different product. No injuries have been reported.
Product
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA = 12 mm, Product Code: 880-601/12
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1372-2025·2025-03-26
Modular Stem Orthopedic Implant Recalled Due to Incorrect Product Identifier
37 units of a modular stem orthopedic implant (Product Code 880-601/11) have been recalled due to an incorrect GTIN product identifier on the carton label, which belongs to a different product. No illnesses or injuries have been reported.
Product
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA = 11 mm, Product Code: 880-601/11
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1371-2025·2025-03-26
Helix Elite SARS-CoV-2 QC Material Recall Due to Potential Ct Value Issues
Microbiologics Inc is recalling Helix Elite Inactivated SARS-CoV-2 quality control material (Lot HE0065-29) because the A549 human cell target may produce late Ct values, potentially affecting test result validity.
Product
Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus (Pellet), Multi-analyte, unassayed quality control material, Catalog Number HE0065N
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1387-2025·2025-03-26
Beckman Coulter DxI 9000 Analyzer Communication Failure Recall
Beckman Coulter recalls certain DxI 9000 immunoassay analyzers due to firmware issues that can cause communication failures, potentially delaying patient result reporting.
Product
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, with Component PCB, TSI/RSI firmware C29278
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·25191·2025-03-20
Bella Pro Series and Cooks espresso machines recalled due to burn and laceration hazards
Sensio recalls about 12,300 Bella Pro Series and Cooks Steam Espresso machines because the brew cup handle can eject forcefully, shattering the carafe. Eight of 18 ejection reports involved burn and laceration injuries.
Product
Bella Pro Series and Cooks Steam Espresso machines
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25193·2025-03-20
Segway Ninebot Max G30P and G30LP KickScooters Recalled for Fall Hazard
The folding mechanism on about 220,000 Segway Ninebot Max G30P and G30LP KickScooters can fail during use, causing the handlebars to fold and posing a fall hazard. Segway has received 68 reports of failures, including 20 injuries.
Product
Segway Ninebot Max G30P and Max G30LP KickScooters
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25188·2025-03-20
Model Year 2025 Ski-Doo and Lynx Snowmobiles Recalled for Engine Mount Failure
Bombardier Recreational Products recalls about 4,144 Model Year 2025 Ski-Doo and Lynx snowmobiles due to engine control module mounts that may break and cause stuck throttle, creating a crash hazard.
Product
Model Year 2025 Ski-Doo and Lynx snowmobiles equipped with a 600R E-TEC, 850 E-TEC or 850 E-TEC Turbo R engine
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25187·2025-03-20
Aiper Seagull Pro Cordless Pool Cleaners Recalled for Fire and Burn Hazards
About 32,660 Aiper Seagull Pro pool cleaners are recalled because the power adapter can overheat and catch fire. The firm reported 19 incidents of melting, smoking or fires, resulting in 5 property damage claims with no injuries.
Product
Aiper Seagull Pro ZT6001 cordless robotic pool cleaners
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25190·2025-03-20
Wireless portable power banks recalled due to fire and burn hazards
VC Group recalls 89,500 MagSafe wireless power banks because lithium-ion batteries can overheat and ignite. The company received 19 fire reports resulting in 10 minor injuries.
Product
VC Group MagSafe Wireless Power Pack Portable Power Banks
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25192·2025-03-20
GIKPAL 10 Drawer Dressers Recalled for Tip-Over and Entrapment Risk to Children
GIKPAL 10 Drawer Dressers sold on Walmart.com are recalled for tip-over and entrapment hazards to children if not anchored to a wall. About 28,590 units were sold between September 2023 and January 2025.
Product
GIKPAL 10 Drawer Dressers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25194·2025-03-20
Benadryl Liquid Elixir 100 mL bottles lack child-resistant packaging
Arsell is recalling Benadryl Liquid Elixir 100 mL bottles sold on Amazon because the packaging is not child-resistant as required by federal law. The medication could poison children if ingested.
Product
Benadryl Liquid Elixir, 100 mL bottles
Category
Drug
Distribution
Distributed nationwide
HighCPSC·25189·2025-03-20
Woolite Delicates Detergent Recalled Due to Bacterial Contamination Risk
Reckitt is recalling approximately 16,200 bottles of Woolite Delicates detergent sold exclusively on Amazon due to potential Pseudomonas bacteria contamination. The bacteria poses a serious infection risk to people with weakened immune systems or external medical devices.
Product
Woolite Delicates detergent in 50-fluid-ounce bottles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25186·2025-03-20
Kimpex Snowmobile Ski Kits Recalled for Detachment Hazard and Crash Risk
Kimpex ski kits for snowmobiles can detach from the vehicle, posing a crash hazard and risk of serious injury. No injuries have been reported to date.
Product
Kimpex Ski and Adaptor Kits
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25184·2025-03-20
Adjustable Dumbbells Recalled for Weight Plate Dislodging Impact Hazard
Weight plates on FitRx SmartBell XL dumbbells can dislodge during use, causing impact injuries. More than 60 incidents reported, linked to 7 documented injuries including bruises and contusions.
Product
FitRx SmartBell XL Quick-Select 10-90 lbs. Adjustable Dumbbells
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1289-2025·2025-03-19
Portex Endotracheal Tubes may deliver inadequate ventilation due to smaller diameter
Portex Endotracheal Tubes from Smiths Medical ASD, Inc. may have a smaller diameter than expected, potentially causing inadequate ventilation and patient hypoxia.
Product
Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127/035 100/141/025 100/141/030 100/141/035
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0609-2025·2025-03-19
Aleppo Tahini Sesame Paste recalled due to Salmonella contamination
Turkana Food Inc. is recalling Aleppo Tahini Sesame Paste because the product tested positive for Salmonella. The recalled product was distributed to 23 states.
Product
Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case
Category
Food
Distribution
23 states
CriticalFDA (Food)·F-0633-2025·2025-03-19
Ulker Biskrem Cocoa Biscuits Recalled for Undeclared Wheat and Egg
ZB Importing LLC recalls Ulker Biskrem Cocoa Biscuits due to undeclared wheat and egg. Consumers with these allergies should not consume the product.
Product
Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628
Category
Food
Distribution
36 states
SevereFDA (Drugs)·D-0268-2025·2025-03-19
Potassium Chloride Injection Strength Mislabeled on Packaging Overwrap
ICU Medical recalls Potassium Chloride Injection (lot 1023172) whose overwrap labeled as 10 mEq may contain 20 mEq containers, creating overdose risk. Product distributed nationwide.
Product
POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0637-2025·2025-03-19
Little Leaf Farms Southwest Salad Kit Recalled for Undeclared Fish and Wheat
Little Leaf Farms Southwest Salad Kit may contain incorrect dressing with undeclared fish and wheat. The recalled lot was distributed in Massachusetts, New Hampshire, and Connecticut.
Product
Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220
Category
Food
Distribution
3 states

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