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

15901–15925 of 27769

HighFDA (Devices)·Z-0082-2024·2023-10-18
RoyalVibe Unapproved Medical Devices Recalled Due to Lack of FDA Authorization
RoyalVibe Health recalled multiple unapproved medical devices including ultrasound generators and therapy devices never FDA-authorized or cleared. Users could forgo legitimate medical treatment based on unproven marketing claims.
Product
CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water Restructuring Pad, RoyalVibe Therapy Balls
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0076-2024·2023-10-18
Medfusion Syringe Pumps Recalled for Force Sensor Calibration Drift
The Medfusion Syringe Pump Model 3500-500 may experience force sensor calibration drift, causing false alarms or delayed occlusion detection. Approximately 20,815 units are being recalled worldwide, with increased risk in devices manufactured before April 2022.
Product
Medfusion Syringe Pump, Model 3500-500, v3, v4, v5, and v6
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0102-2024·2023-10-18
Knee Tibial Insert Recalled Due to Component Mix-Up in Packaging
Encore Medical is recalling the EMPOWR 3D Knee Tibial Insert due to a packaging error where hip and knee components were swapped, potentially causing surgeons to use the wrong implant during surgery.
Product
EMPOWR 3D Knee Tibial Insert, 5R, 10MM, VE, REF: 342-10-705
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0077-2024·2023-10-18
Medfusion Syringe Pump Sensor Calibration Drift May Cause False Alarms
Smiths Medical is recalling Medfusion Model 3500VX-500 Syringe Pumps due to force sensor calibration drift that can cause false alarms, system failures, or delayed occlusion detection.
Product
Medfusion Syringe Pump, Model 3500VX-500, v3, v4, v5, and v6
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0012-2024·2023-10-18
Maisie Jane's Smooth Almond Butter Recalled for High Aflatoxin Levels
Maisie Jane's Smooth almond butter is being recalled due to high levels of aflatoxin contamination. Consumers should discard the product or return it for a refund.
Product
Maisie Jane's Smooth almond butter, 12 oz glass jar, 6 units per case, shelf stable
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-0089-2024·2023-10-18
Cardinal Health Recalls Surgical Procedure Packs Due to Defective Components
Cardinal Health is recalling 13,351 surgical procedure packs distributed nationwide and in Canada. The packs contain recalled equipment drapes, table covers, and surgical room turnover kits.
Product
Procedure packs: (1) Presource PBDS Cat. PNVMNIB21, Kit, Neuro IMAS, Sterile; (2) Presource PBDS Cat. PN08LAG13, Kit, Spine, Sterile; (3) Presource PBDS Cat. PN08LAG17, Kit, Spine, Sterile; (4) Presource PBDS, Cat. PN11SFS40, Kit, Thoracolumbar Fusion, Sterile; (5) Presour
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0109-2024·2023-10-18
Surgical instrument button malfunction may extend operative time
Olympus THUNDERBEAT surgical instruments may have a blue seal button that remains engaged after release, potentially extending surgery time. The company is recalling 271 affected units nationwide.
Product
THUNDERBEAT, 5MM, 45CM, Front-actuated Grip Type S Model: TB-0545FCS Indicated for open, laparoscopic (including single-site surgery) general surgery and gynecological surgery (including urologic, thoracic, plastic and reconstructive, bowel resections, cholecystectomies, Nissen
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0099-2024·2023-10-18
Constellation Vision System surgical units recalled for pressure control defect
Alcon Research recalls Constellation Vision System ophthalmic microsurgical units due to a printed circuit board design flaw that could disable pressure control, risking infection and tissue damage.
Product
Constellation Vision System, REF: 8065751150
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0083-2024·2023-10-18
Cardinal Health procedure packs recalled for containing previously recalled components
Cardinal Health is recalling surgical procedure packs that contain previously recalled components including equipment drapes, table covers, and surgical room turnover kits. Approximately 13,351 packs were distributed nationwide and in Canada.
Product
Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced Surgery Center SAR, Sterile. (2) Presource Block Tray, Catalog SNE37ANMOF, Medical Center Odessa.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V950000·2023-10-12
2022 Acura TLX Tire Damage Recall Due to Bead Cuts and Tears
Honda is recalling approximately 19 model-year 2022 Acura TLX vehicles because their tires may have sustained cuts and tears. Damaged tires can lead to loss of vehicle control and increase crash risk.
Product
ACURA — 2022 ACURA TLX
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24703·2023-10-12
Crystal Clear Sodium Hydroxide 2-lb Bags Lack Child-Resistant Packaging
Family Health Products is recalling Crystal Clear Sodium Hydroxide sold on Amazon because the packaging is not child-resistant as required by law. The product poses a risk of chemical burns and eye irritation if accessed by children.
Product
Crystal Clear Sodium Hydroxide, 2 lb. bags
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V951000·2023-10-12
Motorhomes recalled for faulty LPG service valves causing propane leak risk
Kibbi is recalling 2022–2023 Renegade Valencia motorhomes. Service valves on LPG tanks may be improperly connected, creating a propane leak risk that could lead to fire if an ignition source is present.
Product
RENEGADE — 2023 RENEGADE VALENCIA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V947000·2023-10-12
2022 RAM PROMASTER recalled for inoperative rearview camera
Chrysler recalls 2022 RAM PROMASTER vehicles with an incorrect rearview camera that cannot be installed, reducing rear visibility and increasing crash risk.
Product
RAM — 2022 RAM PROMASTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V949000·2023-10-12
2021-2023 Holiday Rambler and Fleetwood Motorhomes: Propane Tank Valve Defect
REV Recreation Group is recalling certain 2021-2023 Holiday Rambler and Fleetwood motorhomes due to service valve defects on LPG tanks that may cause propane leaks and fire risk. Dealers will replace valves at no cost.
Product
HOLIDAY RAMBLER — 2021 HOLIDAY RAMBLER NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24006·2023-10-12
The FORT Children's Play Tents Recalled for Choking and Laceration Hazards
About 13,250 FORT children's play tents are being recalled because magnets used to connect pieces can come loose, posing choking and laceration risks to young children. The manufacturer is no longer in business and offers no remedy.
Product
The FORT Children's Play Tents
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24008·2023-10-12
Gevi Countertop Nugget Ice Makers Recalled Due to Laceration Hazard
Gevi countertop nugget ice makers with model number GIMN-1102 and a date code before June 1, 2022, are being recalled because metal auger blades can break and create sharp metal pieces in the ice basket, posing a laceration risk. No injuries have been reported.
Product
Gevi Household Countertop Nugget Ice Makers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24702·2023-10-12
YourHealthToolkit Children's Weighted Blankets Recalled for Asphyxiation Hazard
YourHealthToolkit is recalling about 280 children's 5-pound weighted blankets sold on Amazon.com from January through March 2020. A young child can become entrapped inside the blanket by unzipping it, posing a risk of death by asphyxiation.
Product
YourHealthToolkit 5-pound children's weighted blankets
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0037-2024·2023-10-11
FDA Recalls Dr. Berne's MSM Drops Due to Non-Sterility Concerns
Dr. Berne's MSM DROPS 5% Solution was recalled by the FDA for non-sterility issues. Lot 6786, with expiration date March 31, 2025, is distributed nationwide and internationally.
Product
Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, [email protected], UPC 00854582001111.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0001-2024·2023-10-11
Arrow PICC Catheters Recalled for Incorrect Product Label Information
Arrow International recalled 1,173 PICC line units due to incorrect product code and name on packaging labels. Affected lot 33F23B0781 was distributed in the US.
Product
Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet, REF CDC-45552-VPS2; Catheter: Percutaneous Implanted Long-Term Intravascular Catheter Stylet: Diagnostic Intravascular Catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-0004-2024·2023-10-11
FDA Recalls Arrow PICC Catheters with Incorrect Product Code Labels
Arrow INTERNATIONAL recalled 172 units of ErgoPack PICC catheters due to incorrect product code and product name labels. The error affected lot 13F22G0508 distributed in the US.
Product
Arrow ErgoPack Pressure Injectable Arrowg+ard Blue Advance Three-Lumen PICC pre-loaded with Arrow VPS TipTracker Stylet, REF CDC-45563-TTS; catheter, intravascular, therapeutic, long-term greater than 30 days
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-0003-2024·2023-10-11
Arrow Central Venous Catheter Recalled for Incorrect Lidstock Labeling
Arrow International is recalling 380 units of its Arrowg+ard Blue Plus Four-Lumen central venous catheter (model CDC-45854-P1A, lot 13F22L0806) due to incorrect product code and name listed on the package lidstock.
Product
Arrow Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-0002-2024·2023-10-11
Arrow ErgoPack central venous catheter recalled for incorrect labeling
ARROW INTERNATIONAL is recalling 180 units of the Arrow ErgoPack Complete CVC catheter (Lot 33F23B0723) distributed in the US because the product code and product name were incorrectly listed on the kit's label.
Product
Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-1700-2023·2023-10-11
Sweet & Spicy BBQ Sauce Recalled for Undeclared Fish Allergen
The Fresh Chile Company is recalling Sweet & Spicy BBQ sauce due to an undeclared fish (anchovies) allergen on the label. Consumers with fish allergies may be at risk.
Product
Sweet & Spicy BBQ sauce, Fresh Chile BBQ sweet & Spicy Medium. 19 fluid ounce glass jar 19 fl oz. (510g) , with a metal screw top lid.
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-0025-2024·2023-10-11
BD Cathena IV Catheter Safety Shield May Fail to Properly Engage
Becton Dickinson is recalling BD Cathena IV catheters because the safety shield may fail to properly engage, potentially exposing the contaminated needle.
Product
REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx Only, Sterile EO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0009-2024·2023-10-11
Guider Softip Guide Catheter Recalled for Incorrect Tip Curve Shape
Boston Scientific is recalling certain lots of Guider Softip Guide Catheters because they were manufactured with an incorrect tip curve shape that differs from the labeled specification.
Product
Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

15901–15925 of 27769