PlainRecalls

2026 Recalls

2,438 recalls · Page 39 of 49

2026 Recall Year Insight

Federal agencies issued 2,438 product recalls indexed by PlainRecalls in calendar year 2026. That represents about 2.40% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 6.7 recalls per day across the FDA, CPSC, and NHTSA 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 49 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 2 critical, 48 moderate, and 0 lower-severity recalls. The page references 12 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Feb 11, 2026

OXIRIS SET, Product Code 112016; Dialyzer, High Permeability With Or Without Sealed Dialysate System

VANTIVE US HEALTHCARE LLC

FDA Devices Moderate Feb 11, 2026

Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser Probe Curved Cat No. VS0120.25 3. 25GA Laser Probe Flex-Tip Ca…

Vortex Surgical Inc.

FDA Devices Moderate Feb 11, 2026

Vivoo Protein Test

Changchun Wancheng Bio-Electron Co., Ltd.

FDA Devices Moderate Feb 11, 2026

FDR Visionary Suite; Model Number: CH-200; Version: (1) 566-16130-23, (2) 566-16130-31, (3)

FUJIFILM Healthcare Americas Corporation

FDA Devices Moderate Feb 11, 2026

Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC431Q-0730; Software Version: N/A Product Descri…

Olympus Corporation of the Americas

FDA Devices Critical Feb 11, 2026

*HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm; Material Number (UPN): M00553560;

Boston Scientific Corporation

FDA Devices Moderate Feb 11, 2026

PRISMAFLEX M150 SET, Product Code 109990; Dialyzer, High Permeability With Or Without Sealed Dialysate System

VANTIVE US HEALTHCARE LLC

FDA Devices Moderate Feb 11, 2026

Vortex Surgical TID Pharos Illuminated Depressor, VS0801B

Vortex Surgical Inc.

FDA Devices Moderate Feb 11, 2026

Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-411Q-0720 Product Description: These instruments have been designed t…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 11, 2026

Brand Name: CleverCut Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0320; Software Version: N/A Product Descri…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 11, 2026

Vortex Surgical I2 Injection Kit, VS0500

Vortex Surgical Inc.

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

Vortex Surgical 25GA Backflush, VS0270.25; 25GA Backflush Retractable, VS0275.27

Vortex Surgical Inc.

FDA Devices Moderate Feb 11, 2026

PRISMAFLEX TPE2000 SET, Product Code 114093; Dialyzer, High Permeability With Or Without Sealed Dialysate System

VANTIVE US HEALTHCARE LLC

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

PRISMAFLEX HF1000 SET, Product Code 107140; Dialyzer, High Permeability With Or Without Sealed Dialysate System

VANTIVE US HEALTHCARE LLC

FDA Devices Moderate Feb 11, 2026

NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 11, 2026

EMPOWR 3D Knee Tibial Insert 5R 14MM, VE, REF: 342-14-705

Encore Medical, LP

FDA Devices Moderate Feb 11, 2026

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.

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS

Siemens Medical Solutions USA, Inc

FDA Devices Critical Feb 11, 2026

AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm; Material Number (UPN): M00553680;

Boston Scientific Corporation

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

PRISMAFLEX ST150 SET US, Product Code 107640US; Dialyzer, High Permeability With Or Without Sealed Dialysate System

VANTIVE US HEALTHCARE LLC

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

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.

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

Product Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number: 81559 Software Version: Not Applicable Product Description: Lumipulse ¿-Am…

Fujirebio Diagnostics, Inc.

FDA Devices Moderate Feb 11, 2026

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.

FDA Devices Moderate Feb 11, 2026

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.

FDA Devices Moderate Feb 11, 2026

S. Typhi/Para Typhi A Antigen

Changchun Wancheng Bio-Electron Co., Ltd.

FDA Devices Moderate Feb 11, 2026

Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25

Vortex Surgical Inc.

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

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

FDA Devices Moderate Feb 11, 2026

Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model/Catalog Number: 235447 Software Version: Not Applicable Product …

Fujirebio Diagnostics, Inc.

FDA Devices Moderate Feb 11, 2026

TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE, catalog number DWJ318

Tornier, Inc

FDA Devices Moderate Feb 11, 2026

NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 11, 2026

Tecfen Retractable Membrane Polisher, QTPR1267-23

Vortex Surgical Inc.

FDA Devices Moderate Feb 11, 2026

The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips; URIMED Urinalysis Reagent Strips URS-5, Rapid UTI Test Includes Ketones: Leukoc…

Changchun Wancheng Bio-Electron Co., Ltd.

FDA Devices Moderate Feb 11, 2026

Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0320 Product…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 11, 2026

Vivoo pH Test

Changchun Wancheng Bio-Electron Co., Ltd.

FDA Devices Moderate Feb 11, 2026

Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC412Q-0215; Software Version: N/A Product Descrip…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 11, 2026

Vivoo Sodium Test; Vivoo Vitamin C Test; Vivoo Hydration Test

Changchun Wancheng Bio-Electron Co., Ltd.

FDA Devices Moderate Feb 11, 2026

25GA Subretinal Injection Cannula VS0220.25

Vortex Surgical Inc.

FDA Devices Moderate Feb 11, 2026

PRISMAFLEX HF1000 SET, Product Code 107142; Dialyzer, High Permeability With Or Without Sealed Dialysate System

VANTIVE US HEALTHCARE LLC

FDA Devices Moderate Feb 11, 2026

CellMek SPS Sample Preparation System, REF: C44603, with software

Beckman Coulter, Inc.

FDA Devices Moderate Feb 11, 2026

Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive VS0740.23 2. 25GA ACTU8 Forceps Adaptive VS0740.25 3. 25GA ACTU8 Forc…

Vortex Surgical Inc.

FDA Devices Moderate Feb 11, 2026

Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog Number: 235454 Software Version: Not Applicable Product Description: L…

Fujirebio Diagnostics, Inc.

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 - consumer product and vehicle recall feeds for 2026

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2026 across the FDA, CPSC and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.