2025 Recalls
5,015 recalls · Page 85 of 101
2025 Recall Year Insight
Federal agencies issued 5,015 product recalls indexed by PlainRecalls in calendar year 2025. That represents about 5.97% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 13.7 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 101 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 12 critical, 38 moderate, and 0 lower-severity recalls. The page references 19 distinct recalling firms operating in 5 distinct product categories, with 38 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (25), NHTSA (12), CPSC (10), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.
ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box, 100 boxes per Carton, Sterile, Manufactured by W…
Wuxi Medical lnstrument Factory Co., Ltd.
A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate, 12-Hole, Left Intended forFixation of fractures of the distal tibia Model/Catalog Number…
Tyber Medical
A.L.P.S. mvX-MEDIAL TIBIA PLATE 6H LT-Medial Tibia Plate, 6-Hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number:…
Tyber Medical
ASP BIOTRACE Auto Read 60 Steam BI Process Challenge Device, REF 73135.
TERRAGENE S.A.
Brivo MR355, NMRI system
GE Healthcare (China) Co., Ltd.
A.L.P.S. mvX--MEDIAL TIBIA PLATE 12H RT-Medial Tibia Plate, 12-Hole, Right Intended for Fixation of fractures of the distal tibia Model/Catalog Num…
Tyber Medical
BD Alaris Pump Module REF 8100 The BD Alaris System with Guardrails Suite MX is a modular infusion pump and monitoring system for the continuous o…
CareFusion 303, Inc.
A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right Intended Fixation of fractures of the distal tibia. Model/Catalog Number:…
Tyber Medical
A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral Fibula Plate, 10-Hole, Left. Intended Fixation of fractures of the distal…
Tyber Medical
A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number…
Tyber Medical
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate, 6-hole, Right Model/Catalog Number: 770708062
Tyber Medical
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate, 8-hole, Left Intended to bridge or otherwise stabilize bone fragments to …
Tyber Medical
A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate, 4-hole, Left Intended for Fixation of fractures of the distal tibia Mo…
Tyber Medical
SIGNA Creator, SIGNA Explorer, NMRI systems
GE Healthcare (China) Co., Ltd.
Pentax Medical Video Processor- Intended to be used with PENTAX Medical endoscopes, monitors and other peripheral devices for endoscopic diagnosis, t…
Pentax of America Inc
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate, 12-Hole, Right. Intended for Fixation of fractures of the distal tibia …
Tyber Medical
SIGNA MR355, SIGNA MR360, NMRI system
GE Healthcare (China) Co., Ltd.
A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate, 16-Hole, Right Intended Fixation of fractures of the distal tibia Model/Catalog Number…
Tyber Medical
138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 138911-01 BD PYXIS MEDBANK MINI CR-4HH-P 169-115 BD PYXIS MED…
CareFusion 303, Inc.
PENTAX Medical Video Upper GI Scope-Intended to provide optical visualization of (via a video monitor), and therapeutic access to the lower gastroint…
Pentax of America Inc
Brand Name: Leica Biosystems Cryostats Product Name: CM1950 Model/Catalog Number: 1491950C4US Software Version: firmware V3.01
LEICA BIOSYSTEMS NUSSLOCH GMBH
A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate, 4-hole, Right Model/Catalog Number: 770708042
Tyber Medical
A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate, 6-Hole, Right Model/Catalog Number: 770715062 Intended for Fixation of fractures of the …
Tyber Medical
139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS MEDFLEX MN 1000 12HH 139053-01 BD PYXIS MEDFLEX MN 1000 2HH-2FH-3FM 139041-01 BD PYXIS…
CareFusion 303, Inc.
DxC 500 AU Clinical Chemistry Analyzer, REF: C63519, and C63520 with affected software.
BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD.
PENTAX Medical Video Colonoscope- Intended to provide optical visualization of (via a video monitor), and therapeutic access to the lower gastrointe…
Pentax of America Inc
MERCEDES-BENZ 2024: PARKING BRAKE
MERCEDES-BENZ
FORD 2023: BACK OVER PREVENTION:SOFTWARE
FORD
FORD,LINCOLN 2021-2024: POWER TRAIN:AUTOMATIC TRANSMISSION:CONTROL MODULE (TCM/PCM/TECM)
FORD,LINCOLN
FORD,LINCOLN 2021-2022: ELECTRICAL SYSTEM: INTEGRATED TRAILER BRAKE CONTROL
FORD,LINCOLN
FORD 2022-2024: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY
FORD
FORD 2021-2022: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY:MANAGEMENT SYSTEM/ENERGY CONTROL MODULE (BMS/BECM):SOFTWARE
FORD
FORD 2022: POWER TRAIN:AUTOMATIC TRANSMISSION:CONTROL MODULE (TCM/PCM/TECM)
FORD
FORD 2021-2022: POWER TRAIN:AXLE ASSEMBLY:AXLE SHAFT
FORD
AUDI 2024-2025: ELECTRICAL SYSTEM:12V/24V/48V BATTERY
AUDI
FORD 2022: SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE
FORD
FORD 2022-2023: ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL
FORD
ARVA Recalls NEO BT PRO Avalanche Transceivers Due to Risk of Loss of Emergency Transmission; Risk of Serious Injury or Death
Canyon Bicycles USA Recalls Speedmax CF Triathlon Bicycles Due to Fall and Injury Hazards
Costway Recalls Babyjoy High Chairs Due to Entrapment and Suffocation Hazards; Ban on Inclined Sleepers and Violation of Federal Regulations for High…
Goplus Corporation, dba Costway, of Fontana, California
Forever 21 Recalls Children's Pajamas Due to Burn Hazard; Violation of Federal Flammability Regulations; Sold Exclusively by Forever 21
F21 OpCo LLC, dba Forever 21, of Los Angeles, California
Goal Zero Recalls Solar Series Combiner Cables for Solar Panels Due to Fire Hazard
Head Rush Technologies Recalls TRUBLUE iQ and TRUBLUE iQ+ Auto Belays Due to Fall Hazard
Head Rush Technologies, of Louisville, Colorado
Kichler Lighting Recalls Wall Sconces Due to Risk of Electric Shock
P.J. Salvage Recalls Pajama Sets and Robes Due to Burn Hazard; Violation of Federal Flammability Regulations for Children's Sleepwear; Sold Exclusive…
Triangle Tube Recalls Prestige and Aerco Esteem Gas Boilers Due to Carbon Monoxide (CO) Poisoning Hazard; Two Deaths Reported
Burnsen SA, of Belgium
Wayfair Recalls Style Life Eleven Baby Loungers Due to Suffocation Risk and Fall Hazard; Violation of Federal Regulations for Infant Sleep Products; …
Bespoke Clothing Valley Inc., (Royalbelle), d/b/a Zoomie Kids, of China
AUDI 2022-2023: POWER TRAIN:AUTOMATIC TRANSMISSION:GEAR POSITION INDICATION (PRNDL)
AUDI
AAHU BARAH brand SOFT PLUM; NET WT. 0.5 LB; Import By: AAHU BARAH USA, INC.; Soft Plum Aloo Bukahara 1/2 LB; *May Contain Sulfites As preservatives; …
Global Commodities Inc
Wegmans, Organic Almonds Dry Roasted Salted, 12oz clear bag, 12 bags per case.
United Natural Trading Inc. dba Woodstock Farms
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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2025
Read our methodology — how this data is sourced, computed, and verified.