2026 Recalls
905 recalls · Page 11 of 19
2026 Recall Year Insight
Federal agencies issued 905 product recalls indexed by PlainRecalls in calendar year 2026. That represents about 1.08% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 2.5 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS combined. Year-level views are the cleanest way to see macro patterns: volume spikes often correlate with new regulatory priorities (e.g., infant-sleep products after 2021, lithium-ion batteries after 2022), supply-chain contamination events, or changes in agency enforcement intensity, while quiet years can reflect either genuine product-safety improvements or reduced agency staffing and reporting lag. With 19 pages at 50 recalls each, browsing this year end-to-end gives a statistically representative sample of what the federal recall pipeline looked like in 2026.
On this page of 50 records, severity classification shows 5 critical, 45 moderate, and 0 lower-severity recalls. The page references 25 distinct recalling firms operating in 4 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (27), CPSC (19), NHTSA (4), which matters because each agency's recall authority, hazard framing, and remedy mechanism differ — an FDA food recall, a CPSC consumer-product recall, and a NHTSA vehicle recall are legally distinct instruments even when the underlying hazard language sounds similar. Reviewing the dominant agency for a given year is one of the fastest ways to understand where federal attention was concentrated.
Year-indexed browsing serves three practical purposes: historical research (tracking how a hazard class evolved over time), consumer action (finding whether a product purchased in 2026 was later recalled), and journalistic or regulatory context (understanding what the enforcement landscape looked like in a given period). Every record on this page links to a full detail view with the hazard, remedy, distribution, and agency-assigned recall number — always use that recall number to verify current status directly with the issuing agency before acting on time-sensitive remedies, because agencies amend, terminate, and expand recalls in the months and years after initial publication. Data on this page reflects federal agency public filings; the agency's live record remains authoritative for legal, medical, or safety decisions. Verify with FDA openFDA, CPSC, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.
Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number:KD-VC433Q-0730; Software Version: N/A Product Descript…
Olympus Corporation of the Americas
Vortex Surgical 25GA Backflush, VS0270.25; 25GA Backflush Retractable, VS0275.27
Vortex Surgical Inc.
PRISMAFLEX TPE2000 SET, Product Code 114093; Dialyzer, High Permeability With Or Without Sealed Dialysate System
VANTIVE US HEALTHCARE LLC
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0730; Software Version: N/A Product Description: These instrumen…
Olympus Corporation of the Americas
PRISMAFLEX HF1000 SET, Product Code 107140; Dialyzer, High Permeability With Or Without Sealed Dialysate System
VANTIVE US HEALTHCARE LLC
NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS
Siemens Medical Solutions USA, Inc
EMPOWR 3D Knee Tibial Insert 5R 14MM, VE, REF: 342-14-705
Encore Medical, LP
LotFancy Urinary Tract Infection Urine (UTI) Test Strips; PALINOIA UTI-10 PARAMETER REAGENT STRIPS; Vaunn Medical 8-in-1 Urinalysis Reagent Strip; …
Changchun Wancheng Bio-Electron Co., Ltd.
Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0320; Software Version: N/A Product Descrip…
Olympus Corporation of the Americas
SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS
Siemens Medical Solutions USA, Inc
AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm; Material Number (UPN): M00553680;
Boston Scientific Corporation
Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single Use Electrosurgical Knife KD-640L Model/Catalog Number: KD640-L Product …
Olympus Corporation of the Americas
Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0730; Software Version: N/A Product Descrip…
Olympus Corporation of the Americas
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3030 Product Description: These instruments have been designed to …
Olympus Corporation of the Americas
PRISMAFLEX ST150 SET US, Product Code 107640US; Dialyzer, High Permeability With Or Without Sealed Dialysate System
VANTIVE US HEALTHCARE LLC
Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus Single Use Electrosurgical Knife KD-645 Model/Catalog Number: KD-645L Pr…
Olympus Corporation of the Americas
Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number: CL0073 Software Version: Not Applicable Product Description: L…
Fujirebio Diagnostics, Inc.
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3020 Product Description: These instruments have been designed to …
Olympus Corporation of the Americas
Product Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number: 81559 Software Version: Not Applicable Product Description: Lumipulse ¿-Am…
Fujirebio Diagnostics, Inc.
Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Laser Probe OS4 Illuminated Flex-Tip VK401213 3. 23G Laser Probe OS4 Intuitive Exenda…
Vortex Surgical Inc.
MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump is indicated for use by p…
Medtronic MiniMed, Inc.
S. Typhi/Para Typhi A Antigen
Changchun Wancheng Bio-Electron Co., Ltd.
Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25
Vortex Surgical Inc.
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V431M-0730; Software Version: N/A Product Description: These instrumen…
Olympus Corporation of the Americas
Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0330; Software Version: N/A Product Descrip…
Olympus Corporation of the Americas
Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model/Catalog Number: 235447 Software Version: Not Applicable Product …
Fujirebio Diagnostics, Inc.
TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE, catalog number DWJ318
Tornier, Inc
Airova Recalls Aroeve Air Purifiers Due to Fire and Burn Hazards
MERCEDES-BENZ 2022-2024: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY
MERCEDES-BENZ
MERCEDES-BENZ 2020-2023: AIR BAGS: AIR BAG/RESTRAINT CONTROL MODULE
MERCEDES-BENZ
HYUNDAI 2026: STEERING:LINKAGES:KNUCKLE:SPINDLE:ARM
HYUNDAI
HYUNDAI 2025-2026: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY
HYUNDAI
Andy & Evan Recalls Children's Pajama Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwe…
Andy & Evan Industries, Inc., of New York City, New York
Aterian Recalls PurSteam Elite Travel Steamers and Mighty Lil Steamers Due to Risk of Serious Burn Injury
Clark Associates Recalls Lancaster Table & Seating Powder-Coated Aluminum Outdoor Restaurant Chairs and Barstools Due to Fall Hazard
Cobelae Busy Books Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates Small Parts Ban; Sold on Amazon by Flyindream
Shenzhenmengzhongfeikejiyouxiangongsi doing business as Flyindream, of China
Dresbe LED Christmas Headbands Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Produc…
Wenxi Xuefeng Technology Co., Ltd, dba Dresbe, of China
DriBiz Recalls Ammo Tabs Desiccant Tiles Due to Injury Hazard
EnHomee 10-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clot…
Xuzhou Mingquanhe Home Furnishing Co., Ltd., of China
Fixwal 7-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothi…
Changzhou Xunchuang Home Furnishing Co., Ltd., dba Momok of China
Furnulem 5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Sto…
Shanghai Taiye Furniture Co., Ltd., dba Furnulem, of China
GM Gumili Wintergreen Essential Oil Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Chi…
Guangzhou Feifan Kuajing Supply Chain Co., Ltd. dba Gumili Beauty, of China
Kitosun Submersible LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Produ…
Kitosun Original Company Limited, dba Kitosun, of China
Little Cow Company Recalls 9 oz Candles in Glass Jars Due to Fire, Burn and Laceration Hazards
Little Cow Company LLC, of Portland, Oregon
Lola Plus The Boys Recalls Youth Clothing with Drawstrings Due to Risk of Serious Injury or Death from Strangulation Hazard; Violates Federal Rule fo…
Organic Zing Birch Essential Oil Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-…
Salvia Cosmeceuticals, of India
Semfri Children's Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Jinjiangshi XunMai Network Technology Co., Ltd., dba Semfri, of China
Shintenchi 6-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clo…
Huizhou Sunhouse Home Furnishings Co., Ltd., of China
YITA Recalls Multiple Brands of Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for…
Zan International Trading Recalls Lotus Joy Sweet Birch Essential Oil Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates M…
Guangzhou Tenghui Fragrance & Flavor Co., Ltd., of China
Nearby Recall Years
Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.
Data Sources
- Source: FDA openFDA Enforcement API — calendar-year recall filings for food, drugs, and devices
- Source: CPSC + NHTSA + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2026
Read our methodology — how this data is sourced, computed, and verified.