PlainRecalls

2026 Recalls

2,438 recalls · Page 46 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 21 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Jan 21, 2026

MOSAIQ Oncology Information System with Particle Therapy License (License Kit 45700000000IQRO)

Elekta, Inc.

FDA Devices Moderate Jan 21, 2026

VANTAGE GALAN 3T Model MRT-3020/MEXL-3020

Canon Medical System, USA, INC.

FDA Devices Moderate Jan 21, 2026

Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE, REF DYKMBNDL116G

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075 (2.7-7cm,SP1098,Box)

Intuitive Surgical, Inc.

FDA Devices Moderate Jan 21, 2026

BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F

HANGZHOU BEVER MEDICAL DEVICES CO., LTD.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10F; Model Number: 722002;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: DR HOLCOMB FACIAL PACK, Medline kit SKU DYNJ5448…

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Brand Name: PALACOS Product Name: PALACOS R+G pro 40; PALACOS R+G pro 80 Model/Catalog Number: 5081288; 5081289 Software Version: N/A Product Des…

Heraeus Medical GmbH (Dental Division)

FDA Devices Moderate Jan 21, 2026

A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on S…

Medtronic Neuromodulation

FDA Devices Moderate Jan 21, 2026

Medicrea, IB3D PL Instruments Set, Rx Only REF: SPS03174

Medicrea International

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC0102…

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10/10; Model Number: 722027;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD20; Model Number: 722028;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Product Name: Allura Xper FD10C; Model number: 722001;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. A…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10; Model Number: 722003;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE, REF CDS980754T; 2) GYN LAP HYSTERECTOMY CDS, REF CDS982662Q; 3) DAVI…

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) PRE OP KIT, Medline kit SKU DYKS1093B; 2) P…

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.

Mobius Imaging, LLC

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10/10; Model Number: 722011;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2…

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

MAVERICK¿ Measurement Module Spectrometer PN 820-01367 (originally part of a kit PN 820-01519) Finished Goods PN 820-01496

REPLIGEN CORPORATION

FDA Devices Moderate Jan 21, 2026

Allura Xper FD20/20; Model Number: 722038;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972…

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10/10; Model Number: 722005;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD20; Model Number: 722012;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2 4084P-1 4080PE 4080PG

ICU Medical Inc.

FDA Devices Moderate Jan 21, 2026

Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF, REF CDS860235L; 2) GENERAL LAPAROSCOPIC, REF CDS930223M; 3) LAP …

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum of the anti…

Diagnostica Stago, Inc.

FDA Devices Critical Jan 21, 2026

FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Gl…

Abbott Diabetes Care, Inc.

FDA Devices Moderate Jan 21, 2026

ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.

Hologic, Inc

FDA Devices Moderate Jan 21, 2026

VANTAGE TITAN 3T Model MRT-3010/MEXL-3010

Canon Medical System, USA, INC.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD20/10; Model Number: 722029;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) ADMIN KIT, Medline kit SKU DYKS1339B; 2) A…

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

SMV DSI, System, Tomography, Computed, Emission

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING

FDA Devices Moderate Jan 21, 2026

Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label descriptions and corresponding models: 1. Azurion…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.

Fresenius Kabi USA, LLC

FDA Devices Moderate Jan 21, 2026

Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography (CT) X-ray System.

Mobius Imaging, LLC

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10; Model Number: 722010;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Portex Spinal Tray, Item No. A3729-24 A3595

ICU Medical Inc.

FDA Devices Moderate Jan 21, 2026

Medicrea, IB3D Universal Implant Inserter, Rx Only REF: A24000000

Medicrea International

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-PLASTIC CRANIOFACIAL PK-LF, Medline kit SKU…

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: NEURO ANGIO PACK, Medline kit SKU DYNJ38935

Medline Industries, LP

FDA Devices Critical Jan 21, 2026

FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Con…

Abbott Diabetes Care, Inc.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD20 Biplane; Model Number: 722008;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Brand Name: PALACOS Product Name: PALACOS MV pro 40; PALACOS MV pro 80 Model/Catalog Number: 5150633; 5150635 Software Version: N/A Product Descr…

Heraeus Medical GmbH (Dental Division)

FDA Devices Moderate Jan 21, 2026

The product is used for the evaluation of the intrinsic coagulation pathway, APTT substitution test and the monitoring of heparin therapy.

Instrumentation Laboratory

FDA Devices Moderate Jan 21, 2026

CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag Pre-connected Pack, REF: CMAEK00…

Thoratec LLC

FDA Devices Moderate Jan 21, 2026

Plum Duo Infusion System, List Number 40002-04-01

ICU Medical, Inc.

FDA Devices Moderate Jan 21, 2026

Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G12100090 AB9G14080090 AB9G12080090 AB9U12060090 AB9U14100090 AB9U140800…

Medtronic 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.