PlainRecalls

2026 Recall Year Insight

Federal agencies issued 3,961 product recalls indexed by PlainRecalls in calendar year 2026. That represents about 3.79% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 10.9 recalls per day across the FDA, CPSC, USDA FSIS, 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 80 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 13 critical, 37 moderate, and 0 lower-severity recalls. The page references 32 distinct recalling firms operating in 7 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (23), CPSC (19), NHTSA (7), 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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Critical Apr 22, 2026

Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7

Insulet Corporation

FDA Devices Moderate Apr 22, 2026

Yeastone Broth, 11ML, 10/BOX YY3462

Remel, Inc

FDA Devices Moderate Apr 22, 2026

Gentuity HF-OCT Imaging System Model G10-01; Software version 23.2.13;

Gentuity, LLC

FDA Devices Moderate Apr 22, 2026

Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.

Integra LifeSciences Corp. (NeuroSciences)

FDA Devices Moderate Apr 22, 2026

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

Wilson-Cook Medical Inc.

FDA Devices Moderate Apr 22, 2026

Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software Version: Not Applicable Product Description: THERAKOS Photopheresis or extracorporeal photopheresis (ECP) is a photoimmune therapy where leukocytes are separated from whole blood via apheresis, combined with a photoactive drug (8-methoxypsoralen) and then exposed to ultraviolet A (UVA) light. All blood components, including the treated leukocytes, are returned to the patie

THERAKOS DEVELOPMENT LIMITED

FDA Devices Moderate Apr 22, 2026

Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to be used in combination with a Philips interventional X-ray system and 3DRA data.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 22, 2026

iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software

Beta Bionics, Inc.

FDA Devices Moderate Apr 22, 2026

Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL PLATE, ELEGANCE 4 LEVEL CERVICAL PLATE Model/Catalog Number: See Excel sheet attached named "FDA 5072 Product Information" Software Version: Not applicable Product Description: The Elegance¿Anterior Cervical plate is designed for use as a cervical plate system. It has a shape which restores the intervertebral height and lordosis. The Elegance¿

Clariance-SAS

FDA Devices Moderate Apr 22, 2026

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Integra LifeSciences Corp. (NeuroSciences)

FDA Devices Critical Apr 22, 2026

B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.

B Braun Medical Inc

FDA Devices Moderate Apr 22, 2026

Philips Spectral CT on Rails. Model Number: 728334.

PHILIPS MEDICAL SYSTEMS

FDA Devices Moderate Apr 22, 2026

ARTIS Pheno VE30A and VE40A, Model 10849000

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Apr 22, 2026

CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F

Medline Industries, LP

FDA Devices Critical Apr 22, 2026

B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR. Model Number: SL-2010M2096A.

B Braun Medical Inc

FDA Devices Critical Apr 22, 2026

B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.

B Braun Medical Inc

FDA Devices Moderate Apr 22, 2026

Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.

Integra LifeSciences Corp. (NeuroSciences)

FDA Devices Moderate Apr 22, 2026

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

Linkbio Corp.

FDA Devices Critical Apr 22, 2026

B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.

B Braun Medical Inc

FDA Devices Moderate Apr 22, 2026

Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.

Integra LifeSciences Corp. (NeuroSciences)

FDA Devices Moderate Apr 22, 2026

Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.

Integra LifeSciences Corp. (NeuroSciences)

FDA Devices Critical Apr 22, 2026

B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model Number: B3-3632M3705.

B Braun Medical Inc

FDA Devices Critical Apr 22, 2026

B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Number: SL-2010M2096

B Braun Medical Inc

NHTSA No agency class Apr 22, 2026

VOLKSWAGEN 2025: FUEL SYSTEM, GASOLINE:DELIVERY:PRESSURE SENSOR

VOLKSWAGEN

NHTSA No agency class Apr 22, 2026

TOYOTA 2025: SEATS:CRITICAL FASTENERS

TOYOTA

NHTSA No agency class Apr 22, 2026

TESLA 2024-2026: WHEELS:LUGS/NUTS/BOLTS/STUDS

TESLA

NHTSA No agency class Apr 21, 2026

HYUNDAI 2025-2026: AIR BAGS:SENSOR:SIDE IMPACT

HYUNDAI

NHTSA No agency class Apr 20, 2026

MITSUBISHI 2014-2022: STRUCTURE:BODY:HATCHBACK/LIFTGATE:SUPPORT DEVICE/STRUT

MITSUBISHI

NHTSA No agency class Apr 17, 2026

JAGUAR,LAND ROVER 2019-2024: ELECTRICAL SYSTEM:PROPULSION SYSTEM:DC/DC CONVERTER

JAGUAR,LAND ROVER

CPSC No agency class Apr 16, 2026

Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by ZOLIQUEX

ZOLIQUEX, of China

CPSC No agency class Apr 16, 2026

Agiiman Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards

Jiangxi Runfuyuan Biotechnology Co., Ltd dba Agiiman, of China

CPSC No agency class Apr 16, 2026

Apex Gaming PCs Recalls Manik and Apex-branded ATX Computer Power Supplies Due to Risk of Serious Injury or Death from Electrical Shock and Electrocution Hazards

CPSC No agency class Apr 16, 2026

ATOYUS Children's Activity Cubes Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban and Mandatory Standard for Toys; Sold on Amazon by Melofaver US

Shen Zhen Zhuoyuechaoqun Electronic Commerce Co., Ltd., dba Melofaver US, of China

CPSC No agency class Apr 16, 2026

Fengrong Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards

Ningboaonadianzishangwuyouxiangongsi., dba Fengrong Tool, of China

CPSC No agency class Apr 16, 2026

Free-Standing Professional Gas Ranges Recalled Due to Risk of Burn Hazard; Manufactured by Fisher & Paykel

Fisher & Paykel Appliances (Thailand) Co., Ltd, of Thailand

CPSC No agency class Apr 16, 2026

Fun and Function Recalls Children's Metal Multi-Point Swing Frames Due to Risk of Injury from Fall Hazard

CPSC No agency class Apr 16, 2026

Generac Power Systems Recalls Portable Generators Due to Risk of Serious Injury or Death from Burn and Fire Hazards

CPSC No agency class Apr 16, 2026

JC Sales Recalls Lil' Buddies Pet Laser Toys Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries

CPSC No agency class Apr 16, 2026

Le Hao Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards

Ningbofenghuaxinlehaodianziyouxiangongsi, dba Le Hao Tool, of China

CPSC No agency class Apr 16, 2026

Macy's Recalls Arch Studio Tea Kettles Due to Risk of Serious Injury from Burn Hazard

CPSC No agency class Apr 16, 2026

Mini Round Toddler Trampolines Recalled Due to Strangulation Hazard; Risk of Serious Injury or Death; Manufactured by SEGMART

Shenzhen Segmart Technology Electronics Co., Ltd., of China

CPSC No agency class Apr 16, 2026

Montessori Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Mandatory Standard for Teething Toys; Sold on Amazon by SpringFlower

Shantou Ai Xing Trading Co., Ltd., dba SpringFlower, of China

CPSC No agency class Apr 16, 2026

nvyue Magic Pocket Staffs Recalled Due to Projectile and Laceration Hazards; Imported by Xingwenfeng

CPSC No agency class Apr 16, 2026

Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by BAYOTAK USA

CPSC No agency class Apr 16, 2026

Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by Patoolio Direct

CPSC No agency class Apr 16, 2026

Sanlebi Pet Vet Playsets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Letokids

Guangzhou Letao Keji Youxiangongsi, doing business as Letokids, of China

CPSC No agency class Apr 16, 2026

Sweetcrispy Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards

Zhejiang Hengjian Home Furnishing Co Ltd., dba Sweetcrispy, of China

CPSC No agency class Apr 16, 2026

ZMC Group Recalls LED Finger Beam Lights Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys

NHTSA No agency class Apr 16, 2026

RAM 2026: ELECTRONIC STABILITY CONTROL (ESC):CONTROL MODULE

RAM

FDA Food Moderate Apr 15, 2026

Crab Cakes various sizes sold to food service

Connecticut Crab Company LLC

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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2026

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2026 across the FDA, CPSC, USDA FSIS 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 September 2026.