PlainRecalls

2025 Recalls

6,168 recalls · Page 86 of 124

2025 Recall Year Insight

Federal agencies issued 6,168 product recalls indexed by PlainRecalls in calendar year 2025. That represents about 6.06% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 16.9 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 124 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 18 critical, 32 moderate, and 0 lower-severity recalls. The page references 20 distinct recalling firms operating in 4 distinct product categories, with 44 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (40), NHTSA (6), CPSC (4), 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Critical May 7, 2025

GE Healthcare Carestation 650 SE, Model/REF Number 1012-9650-012. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Moderate May 7, 2025

Medline Sterile Water, USP, 100mL, REF RDI30295

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate May 7, 2025

IceSeed 1.5 CX NEEDLE OUS, Cryoablation Needle, REF H7493967534170. The needles are intended to convert high-pressure gas to either a very cold Free…

Boston Scientific Corporation

FDA Devices Moderate May 7, 2025

Medline procedure kits, labeled as: REDDY JOINT BATH, REF MMJB001A

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Critical May 7, 2025

GE Healthcare Carestation 620 A1, Model/REF Number 1012-9620-200. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 650 A2, Model/REF Number 1012-9650-002. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 650C A2, Model/REF Number 1012-9655-002. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Moderate May 7, 2025

Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual language), DCF-E2210-F3/1¿(French/English dual …

Defibtech, LLC

FDA Devices Critical May 7, 2025

GE Healthcare Carestation 620 SE, Model/REF Number 1012-9620-012. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Moderate May 7, 2025

Brand Name: Quantum Informatics - VIPER Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or Alarms) Product Description:…

Spectrum Medical Ltd.

FDA Devices Moderate May 7, 2025

epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515; epoc Software Version & Sensor Configura…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate May 7, 2025

Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Numbers: TFL-SLS, TFL-PLS Product D…

Olympus Corporation of the Americas

FDA Devices Moderate May 7, 2025

IceSeed 1.5 CX S NEEDLE US, Cryoablation Needle, REF H7493967233100. The needles are intended to convert high-pressure gas to either a very cold Fre…

Boston Scientific Corporation

FDA Devices Moderate May 7, 2025

Hyperthermia Pump Procedure Kit. Model Number: 902-00045. Sterile, single-use, disposable set used with the Hyperthermia Pump. The Hyperthermia…

Belmont Instrument LLC

FDA Devices Moderate May 7, 2025

Enhanced Verify Evaluation Handset (CFN HH90130FA)

Medtronic Neuromodulation

FDA Devices Moderate May 7, 2025

Automated External Defibrillators, Model DDU-2450. Item number: DCF-E2460DE (German language)

Defibtech, LLC

FDA Devices Moderate May 7, 2025

Distal Femoral Augment; Item Numbers: (1) 880-300/11 (Sz. 0 - cemented sm), (2) 880-300/21 (Sz. 0 - cemented lg), (3) 880-301/11 (Sz. 1-2 - cemented …

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 750c A2, Model/REF Number 1012-9755-002. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 650 A1, Model/REF Number 1012-9650-000. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Critical May 7, 2025

GE Healthcare Carestation 650 A1, Model/REF Number 1012-9650-200. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Moderate May 7, 2025

Stratus CS Acute Care cTNI TestPak.IVD test for cardiac troponin I in heparinized plasma.

Siemens Healthcare Diagnostics Inc

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 750 A1, Model/REF Number 1012-9750-000. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Moderate May 7, 2025

Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual language), DCF-E2210-F3/1¿(French/English dual …

Defibtech, LLC

FDA Devices Moderate May 7, 2025

Medline procedure kits, labeled as: OL OCULAR, REF DYNJ906183K

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate May 7, 2025

The Trimble RTS873 robotic total station is a solution designed for construction professionals seeking precision, efficiency, and reliability in thei…

Trimble Ab

FDA Devices Moderate May 7, 2025

Straight Inflow/Outflow Patient Line Kit. Model Number: 902-00037. Sterile, single-use, disposable set used with the Hyperthermia Pump. The Str…

Belmont Instrument LLC

FDA Devices Moderate May 7, 2025

Brand Name: Quantum Informatics - VISION / LIVE VUE Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or Alarms) Product …

Spectrum Medical Ltd.

FDA Devices Moderate May 7, 2025

Medline procedure kits, labeled as: PLASTICS SUTURE TRAY, REF SUT13535

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate May 7, 2025

L-Shaped Femoral Augment; Item Numbers: (1) 880-320/12 (Sz. 0 - cemented sm), (2) 880-320/22 (Sz. 0 - cemented lg), (3) 880-321/12 (Sz. 1-2 - cemente…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate May 7, 2025

HistoCore PELORIS 3, Model/Catalog Number: 45.0005/45.7512.501 A11, Software Version: 3.4.0. The HistoCore PELORIS 3 Rapid Tissue Processor is a dua…

Leica Biosystems Melbourne Pty Ltd

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 620 A1, Model/REF Number 1012-9620-000. anesthesia systems

GE Medical Systems China Co., Ltd.

FDA Devices Moderate May 7, 2025

Medline procedure kits, labeled as: 1) WOUND CARE TRAY, REF DYNDA1412A; 2) LACERATION TRAY, REF DYNDL1263A.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 750c A1, Model/REF Number 1012-9755-000. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Moderate May 7, 2025

Medline procedure kits, labeled as: NON STERILE I&D KIT, REF DYKM1438

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate May 7, 2025

Automated External Defibrillators, Model DDU-2300. Item numbers: DCF-E2310D3/1¿(German/English dual language), DCF-E2310E3/1¿(German/French dual lang…

Defibtech, LLC

FDA Devices Critical May 7, 2025

GE Healthcare Carestation 650c A1, Model/REF Number 1012-9655-200. Anesthesia system.

GE Medical Systems China Co., Ltd.

FDA Devices Moderate May 7, 2025

Medline procedure kits, labeled as: HAND, REF DYNJ902002J

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate May 7, 2025

Straight Inflow/Bifurcated Outflow Line Kit. Model Number: 902-00038. Sterile, single-use, disposable set used with the Hyperthermia Pump. The …

Belmont Instrument LLC

FDA Devices Moderate May 7, 2025

IceSeed 1.5 CX NEEDLE US, Cryoablation Needle, REF H7493967433170. The needles are intended to convert high-pressure gas to either a very cold Freez…

Boston Scientific Corporation

FDA Devices Moderate May 7, 2025

epoc BGEM Crea Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736382; epoc Software Version & Sensor Configur…

Siemens Healthcare Diagnostics Inc

NHTSA Critical May 7, 2025

FREIGHTLINER 2025: SERVICE BRAKES, AIR:SUPPLY:RESERVOIR/TANK

FREIGHTLINER

NHTSA Critical May 7, 2025

AUDI 2022-2024: ENGINE

AUDI

NHTSA Critical May 7, 2025

POLESTAR 2025: BACK OVER PREVENTION:SOFTWARE

POLESTAR

NHTSA Critical May 6, 2025

HYUNDAI 2025: POWER TRAIN:AUTOMATIC TRANSMISSION:FLUID/LUBRICANT:PUMP

HYUNDAI

NHTSA Critical May 5, 2025

PORSCHE 2022-2023: AIR BAGS:SENSOR:OCCUPANT CLASSIFICATION:FRONT PASSENGER

PORSCHE

NHTSA Critical May 2, 2025

MERCEDES-BENZ 2022-2024: SEAT BELTS:FRONT

MERCEDES-BENZ

CPSC Moderate May 1, 2025

Baseus Portable Chargers Recalled Due to Fire Hazard; Sold on Amazon.com by Shenzhen Baseus Technology

CPSC Moderate May 1, 2025

Dlesot Snap Children's Hair Clips Recalled Due to Lead Poisoning Hazard; Violation of Federal Ban for Lead in Paint; Sold Exclusively on Amazon by YF…

YuanQuXianXianQiDianZiShangWuYouXianZeRenGongSi, (dba YFLGOTOO), of China

CPSC Moderate May 1, 2025

Kohl's Recalls Tea Light Candle Holders Due to Fire Hazard

CPSC Moderate May 1, 2025

Kubota Tractor Corporation Recalls RTV-Series Utility Vehicles Due to Crash Hazard

Kubota Tractor Corporation, of Grapevine, Texas

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: CPSC + NHTSA - consumer product and vehicle recall feeds for 2025

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 2025 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 August 2026.