PlainRecalls

2025 Recall Year Insight

Federal agencies issued 6,236 product recalls indexed by PlainRecalls in calendar year 2025. That represents about 5.97% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 17.1 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 125 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 2025.

On this page of 50 records, severity classification shows 26 critical, 24 moderate, and 0 lower-severity recalls. The page references 21 distinct recalling firms operating in 3 distinct product categories, with 40 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (40), NHTSA (7), USDA FSIS (3), 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 2025 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 Oct 8, 2025

MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. MAGNETOM Spectra (CN). Model Number: 10655588.

Siemens Medical Solutions USA, Inc

FDA Devices Critical Oct 8, 2025

Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological mapping of cardiac structures. Medline Item Numbers BD710DF282CRH BD710DF282RRH BD710FJ282CRH BD710FJ282RRH

Medline Industries, LP

FDA Devices Critical Oct 8, 2025

MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217.

Siemens Medical Solutions USA, Inc

FDA Devices Critical Oct 8, 2025

Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q

Medline Industries, LP

FDA Devices Critical Oct 8, 2025

MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

Siemens Medical Solutions USA, Inc

FDA Devices Critical Oct 8, 2025

MAGNETOM Vida Fit. Model Number: 11410481.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Oct 8, 2025

Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 8, 2025

NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions.

Northeast Scientific Inc.

FDA Devices Moderate Oct 8, 2025

Allura Xper FD20 Biplane OR Table; Model Numbers: (1) 722020, (2) 722025; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Oct 8, 2025

MAGNETOM Skyra fit. Model Number: 10849580.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Oct 8, 2025

Allura Xper CV20; Model Numbers: 722031; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Oct 8, 2025

Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates. The device can be used for mechanical ventilation, manual ventilation, pressure-supported spontaneous breathing, and spontaneous breathing. The device is specified for inhalational anesthesia and/or patient ventilation in accordance with the intended use durin

Draeger, Inc.

FDA Devices Moderate Oct 8, 2025

Allura Xper FD20 Biplane; Model Numbers: (1) 722008, (2) 722013; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 8, 2025

Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616, (2) AG 630, (3) AG 636, (4) AG 640, (5) AG 645, (6) AG 715, (7) AG 730, (8) AG 735, (9) AG 740, (10) AG 745, (11) AG 750, (12) AG 830, (13) AG 840, (14) AG 1015, (15) AG 1030;

LeMaitre Vascular, Inc.

FDA Devices Moderate Oct 8, 2025

Allura Xper FD20/20; Model Numbers: 722038; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 8, 2025

Cardio Vascular-Allura Centron; Model Numbers: 722400; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 8, 2025

VITEK¿ 2 Gram-negative AST Test Kits (Cards) containing Colistin formulation cs02n. VITEK¿ 2 is an automated system consisting of instruments, software and reagent cards designed for the identification and antimicrobial susceptibility testing of bacteria and yeast. Export only

bioMerieux, Inc.

FDA Devices Moderate Oct 8, 2025

Allura Xper FD20/15 OR Table; Model Numbers: 722059; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 8, 2025

NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-151. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US.

Northeast Scientific Inc.

FDA Devices Critical Oct 8, 2025

Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Number: DYNJ61038B

Medline Industries, LP

FDA Devices Moderate Oct 8, 2025

Allura Xper FD20 OR Table; Model Numbers: (1) 722015, (2) 722023, (3) 722035; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Oct 8, 2025

MAGNETOM Cima.X (DE). Model Number: 11647158.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Oct 8, 2025

NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-159. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US.

Northeast Scientific Inc.

FDA Devices Moderate Oct 8, 2025

Allura Xper FD20; Model Numbers: (1) 722006, (2) 722012, (3) 722028; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 8, 2025

NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter. Model/Catalog Number: R-410-154. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US.

Northeast Scientific Inc.

FDA Devices Critical Oct 8, 2025

MAGNETOM Verio Dot Upgrade. Model Number: 10684334.

Siemens Medical Solutions USA, Inc

FDA Devices Critical Oct 8, 2025

Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during diagnostic electrophysiologic studies; Medline Item Numbers 81102RH 81104RH 81107RH 81174RH 81402RH 81404RH 81405RH 81472RH 81473RH 81474RH 81531RH 81532RH

Medline Industries, LP

FDA Devices Moderate Oct 8, 2025

DxC 500 AU Module w/ISE, DxC 500i, With ISE, REF: C63522 and DxC 500 AU Module, DxC 500i, Without ISE, REF: C6352; part of the DxC 500i Clinical Analyzer

Beckman Coulter Inc.

FDA Devices Moderate Oct 8, 2025

IMPLANT EPIKUT PLUS MT16 3,5X10,0MM, REF: ILM 3510N; IMPLANT EPIKUT PLUS MT16 3.8X11.5MM, REF: ILM 3511N; IMPLANT EPIKUT PLUS MT16 3,5X13,0MM, REF: ILM 3513N; IMPLANT EPIKUT PLUS MT16 3,5X15,0MM, REF: ILM 3515N; IMPLANT EPIKUT PLUS MT16 3,8X10,0MM, REF: ILM 3810N; IMPLANT CM16 3,8 X 11MM, REF: ILM 3811N; IMPLANT EPIKUT PLUS MT16 3,8X15,0MM, REF: ILM 3815N; IMPLANT EPIKUT PLUS MT16 4,0X10,0MM, REF: ILM 4010N; IMPLANT EPIKUT PLUS MT16 4,0X11,5MM, REF: ILM 4011N; IMPLANT EPIKUT PLUS

S.I.N. Implant System Ltda

FDA Devices Moderate Oct 8, 2025

Allura Xper FD10/10; Model Numbers: (1) 722005, (2) 722011, (3) 722027; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Oct 8, 2025

Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart. For imaging guidance only, not treatment delivery, during cardiac interventional percutaneous procedures. Medline Item Numbers 10135910RH 10135936RH

Medline Industries, LP

FDA Devices Critical Oct 8, 2025

MAGNETOM Connectom.X. Model Number: 11371480.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Oct 8, 2025

Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring anomalies in the Venclose EVSRF Ablation Catheter prior to use. The Venclose digiRF Generator is a sophisticated multi-voltage energy delivery system featuring touchscreen control that automatically configures non-adjustable treatment parameters (including time and temperature) for compatible catheters connected via a triaxial connector port. Designed for use with Venclose RF Catheters (either the E

Bard Peripheral Vascular Inc

FDA Devices Critical Oct 8, 2025

MAGNETOM Prisma. Model Number: 10849582.

Siemens Medical Solutions USA, Inc

FDA Devices Critical Oct 8, 2025

Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and other devices within the heart. Medline Item Numbers D087031RH

Medline Industries, LP

FDA Devices Critical Oct 8, 2025

BIOGRAPH One (DE). Model Number: 11689172.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Oct 8, 2025

GORE ACUSEAL Vascular Graft, REF: ECH050020J, ECH050020W, ECH050050J, ECH050050W, ECH060010A, ECH060020A, ECH060020J, ECH060020W, ECH060040, ECH060040A, ECH060040W, ECH060050A, ECH060050J, ECH460045A, ECH460045J, ECH470045, ECH470045A; used with Instructions for Use.

W L Gore & Associates, Inc.

FDA Devices Moderate Oct 8, 2025

AESCULAP ELAN 4 FIXED DURAGUARD LONG. Model Number: GB943R.

Aesculap AG

FDA Devices Critical Oct 8, 2025

MAGNETOM Verio Dot. Model Number: 10684333.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Oct 8, 2025

NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-152. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US.

Northeast Scientific Inc.

NHTSA No agency class Oct 8, 2025

BMW 2026: VISIBILITY:WINDSHIELD:CRITICAL FASTENERS

BMW

NHTSA No agency class Oct 7, 2025

LUCID 2022-2025: BACK OVER PREVENTION:SOFTWARE

LUCID

NHTSA No agency class Oct 7, 2025

LUCID 2024-2026: POWER TRAIN:DRIVELINE:DRIVESHAFT

LUCID

NHTSA No agency class Oct 7, 2025

TOYOTA 2025: SEATS:MID/REAR ASSEMBLY

TOYOTA

NHTSA No agency class Oct 7, 2025

ALFA ROMEO 2020-2025: BACK OVER PREVENTION:DISPLAY FUNCTION

ALFA ROMEO

USDA FSIS Moderate Oct 7, 2025

FSIS Issues Public Health Alert For Ready-To-Eat Meals Containing Riced Cauliflower That May Be Contaminated With Listeria

Freshrealm; FreshRealm

NHTSA No agency class Oct 6, 2025

MACK 2019-2025: SEAT BELTS:FRONT:ANCHORAGE

MACK

NHTSA No agency class Oct 6, 2025

RAM 2024-2025: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION MOTOR:CONTROLLER:SOFTWARE

RAM

USDA FSIS Moderate Oct 6, 2025

FSIS Issues Public Health Alert For Ready-To-Eat Meals Containing Spinach That May Be Contaminated With Listeria

FreshRealm; FreshRealm; FreshRealm

USDA FSIS Critical Oct 4, 2025

Foster Poultry Farms, LLC Recalls Chicken Corn Dog and Ground Turkey on a Stick Products Due To Possible Extraneous Matter Contamination

Foster Poultry Farms, LLC

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2025 with 2024 →

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 2025

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 2025 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.