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 12 critical, 38 moderate, and 0 lower-severity recalls. The page references 23 distinct recalling firms operating in 1 distinct product categories, with 48 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, 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 Moderate Jun 10, 2026

BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet

CareFusion 303, Inc.

FDA Devices Moderate Jun 10, 2026

Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;

Bayer Medical Care, Inc.

FDA Devices Moderate Jun 10, 2026

Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jun 10, 2026

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product Description: Preface: This report under 21 CFR 806.10 is being submitted for the dV5 system tower, as the NIR Handheld Camera or SOCK is developed and integrated as part of the dV5 system. The affected component of the dV5 system tower is the NIR handheld camera, and is supplied by Schoelly as the manufacturer. Therefore, the product description in this report references t

Intuitive Surgical, Inc.

FDA Devices Moderate Jun 10, 2026

BD Pyxis Mini Main REF: 349 Medication cabinet

CareFusion 303, Inc.

FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.

Becton Dickinson & Company

FDA Devices Moderate Jun 10, 2026

Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E

Kico Knee Innovation Company

FDA Devices Moderate Jun 10, 2026

Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System

Stryker Corporation

FDA Devices Critical Jun 10, 2026

Pediatric care bed; Product Designation: KayserBett IDA;

KAYSERBETTEN GMBH & CO. KG

FDA Devices Moderate Jun 10, 2026

Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4

Daavlin Distributing Company

FDA Devices Moderate Jun 10, 2026

Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jun 10, 2026

MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph

GE Medical Systems China Co., Ltd.

FDA Devices Moderate Jun 10, 2026

Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 Model/Catalog Number: 555884 Software Version: N/A Product Description: CESK SHANDS JACKSONVILLE 20055717 Component: No

B Braun Medical Inc

FDA Devices Moderate Jun 10, 2026

BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet

CareFusion 303, Inc.

FDA Devices Moderate Jun 10, 2026

Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid Scala Model/Catalog Number: CI-1601-04 Software Version: N/A Product Description: The HiResolution Bionic Ear System is a cochlear implant designed to provide useful hearing to individuals with severe-to-profound hearing loss. It consists of internal and external components. The internal components include the HiRes" Ultra 3D receiver and either the HiFocus" SlimJ electrode or the HiFocus" Mid-Scala (MS)

Advanced Bionics, LLC

FDA Devices Moderate Jun 10, 2026

Brand Name: B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED TIP CATH Model/Catalog Number: 530201 Software Version: N/A Product Description: NES1725KFXL SPINAL EPID CLOSED TIP CATH Component: No

B Braun Medical Inc

FDA Devices Moderate Jun 10, 2026

COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code: 60884522007028 The devices are intended for use in providing tracheal access for airway management. Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable inner cannulae (LPC, FEN, CFS, CFN, LGT) and twist-lock connectors. These Shiley Tracheostomy Tubes have a radiopaque, biocompatible outer cannula constructed of polyvinyl chloride.

Covidien LLC

FDA Devices Moderate Jun 10, 2026

Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jun 10, 2026

BD Pyxis MedStation ES REF: 323 Medication cabinet

CareFusion 303, Inc.

FDA Devices Moderate Jun 10, 2026

Brand Name: B. BRAUN MEDICAL INC. Product Name: BPSK, BLOCKJOCKS TRAY Model/Catalog Number: 570246 Software Version: N/A Product Description: BPSK, BLOCKJOCKS TRAY Component: No

B Braun Medical Inc

FDA Devices Moderate Jun 10, 2026

Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jun 10, 2026

ARTIS Icono biplane, floor and ceiling.: ARTIS icono biplane Model 11327600. ARTIS icono ceiling Model 11328100. ARTIS icono floor Model 11327700. interventional fluoroscopic x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jun 10, 2026

Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jun 10, 2026

TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis

Grace Medical, Inc.

FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.

Becton Dickinson & Company

FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.

Becton Dickinson & Company

FDA Devices Moderate Jun 10, 2026

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Oculus Technologies of Mexico, S.A. de C.V.

FDA Devices Critical Jun 10, 2026

Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868); P25BKAY PENCAN SPINAL TRAY (333865); P27BK PENCAN SPINAL W/BUPIVAC (333871); P25BK SPINAL TRAY (333851)

B Braun Medical Inc

FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.

Becton Dickinson & Company

FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.

Becton Dickinson & Company

FDA Devices Moderate Jun 10, 2026

ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.

Becton Dickinson & Company

FDA Devices Moderate Jun 10, 2026

The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.

Fresenius Kabi USA, LLC

FDA Devices Moderate Jun 10, 2026

BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet

CareFusion 303, Inc.

FDA Devices Moderate Jun 10, 2026

Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D150BC-40 / D150VC-40 / D150LC-40 / D150LC-40E/D150BC-41 / D150VC-41 / D150LC-41; Digital Radiography System RADspeed safire: UD150B-40 / D150BC-40; Radiography System RADspeed fit: N/A (Integrated in the system); X-RAY R/F

Shimadzu Medical Systems

FDA Devices Moderate Jun 10, 2026

Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife

SSC- Surgical Specialties Corporation

FDA Devices Moderate Jun 10, 2026

DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)

DeRoyal Industries Inc

FDA Devices Moderate Jun 10, 2026

BD Pyxis MedStation 4000 REF: 303 Medication cabinet

CareFusion 303, Inc.

FDA Devices Moderate Jun 10, 2026

Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044

Covidien LLC

FDA Devices Moderate Jun 10, 2026

Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042

Covidien LLC

FDA Devices Moderate Jun 10, 2026

Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C

Kico Knee Innovation Company

FDA Devices Moderate Jun 10, 2026

Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;

Covidien, LP

FDA Devices Moderate Jun 10, 2026

Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.

Becton Dickinson & Company

FDA Devices Critical Jun 10, 2026

Atlan A350. Model Number: 8211500. anesthesia workstation

Draeger, Inc.

FDA Devices Moderate Jun 10, 2026

CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3

GE Medical Systems Information Technologies Inc

FDA Devices Moderate Jun 10, 2026

Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID Model/Catalog Number: 530184 Software Version: N/A Product Description: LYNDON B JOHNSON HOSPITAL SPINAL EPID Component: No

B Braun Medical Inc

FDA Devices Critical Jun 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.

Becton Dickinson & Company

FDA Devices Moderate Jun 10, 2026

BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet

CareFusion 303, Inc.

FDA Devices Critical Jun 10, 2026

LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.

Fresenius Kabi USA, 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.