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 2 critical, 17 moderate, and 31 lower-severity recalls. The page references 14 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 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 Low Sep 3, 2025

C8-4v Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2; All Software Versions.

MAQUET GMBH

FDA Devices Low Sep 3, 2025

L9-3 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals utilizing them. The kit is provided sterile, single-use and includes a range of components dependent upon the specific procedure. These kits will be assembled using Medline and other manufacturers medical device components and drug components in some cases. Customers specify the kit contents, quantity, and placement of individual items in the kit.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Low Sep 3, 2025

X7-2 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

GE HealthCare OEC 9900 Elite C-arm Systems.

GE Medical Systems, LLC

FDA Devices Moderate Sep 3, 2025

Brand Name: HOMEDICS Product Name: Air Compression Leg Massager Model/Catalog Number: SR-160HJ Product Description: Powered Inflatable Tube Massager used on the leg. The Air Compression Leg Massager is indicated for the temporary relief of minor muscle aches and pains and for temporary increase in circulation to the treated areas in people who are in good health. The Air Compression Leg Massager simulates kneading and stroking of tissues by using an inflatable garment.

Zhejiang Luyao Electronics Technology Co., Ltd.

FDA Devices Critical Sep 3, 2025

Battery Operated infusion pumps. t:slim X2 G5, Replacement, Refurbished, REF: 1000911; t:slim X2 GS Classic, Replacement, Refurbished, REF: 1003808; t: slim X2, Basal-IQ, mg/dl, REF: 1004219; Pump, t:slim X2, Clinical Use Only, REF: 1004484; Pump, t:slim X2, Control-IQ, REF: 1005611; Pump, t:slim X2, Control-IQ, mmoUL, Refurbished Replacement, REF: 1005613; Pump, t:slim X2, Control-IQ, mg/dl, REF: 1005615; Pump, t:slim X2, Control-IQ, mg/dl, Refurbished Replacement, REF: 1005617; Pump,

Tandem Diabetes Care, Inc.

FDA Devices Low Sep 3, 2025

S9-2 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Critical Sep 3, 2025

Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Catheter Models 401150RH, 401206RH, 401207RH, 401210RH, 401211RH, 401212RH, 401222RH, 401223RH, 401226RH, 401227RH, 401228RH, 401260RH, 401261RH, 401271RH, 401305RH, 401306RH, 401309RH, 401310RH, 401311RH, 401312RH, 401317RH, 401353RH, 401357RH, 401381RH, 401392RH, 401399RH, 401400RH, 401425RH, 401430RH, 401433RH, 401434RH, 401435RH, 401436RH, 401438RH, 401441RH, 401442RH, 401445RH, 401443RH, 401444RH

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Low Sep 3, 2025

C8-5 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) BORN ON ARRIVAL KIT, Model/Item Number LLBN11C; 2) LABOR & DELIVERY PACK, Model/Item Number LLLD19I.

American Contract Systems Inc

FDA Devices Low Sep 3, 2025

mC7-2 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

C5-2 Lumify Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Spectrum IQ Infusion Pump, Product Code 3570009

Baxter Healthcare Corporation

FDA Devices Moderate Sep 3, 2025

GE HealthCare OEC 9800.

GE Medical Systems, LLC

FDA Devices Low Sep 3, 2025

X6-1 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

C9-3v Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

L12-4 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

BP10-5ec Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

SCNHD LA L7-4 HDI Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

L8-4 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

7.5MHZ Endo Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Orascoptic Superior Visualization Phantom Nose Pad Accessory Kit ( nose pad and screw) 1 pk. and 20 pk.

Orascoptic Surgical Acuity

FDA Devices Low Sep 3, 2025

L10-4LAP Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

C10-4ec Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissue temperature for temporary increase in local blood circulation, temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, muscle spasm, and temporary relaxation of muscles. Component: N/A

THOR Photomedicine Ltd

FDA Devices Low Sep 3, 2025

X5-1 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

PrisMax V2-US, Hemodialysis Delivery System, Product Codes: 955626, 955558, 955627, 955701

VANTIVE US HEALTHCARE LLC

FDA Devices Moderate Sep 3, 2025

AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) SFCH CRANI PACK (PS 132432), MODEL/ITEM NUMBER UICR10W; 2) SFCH SHUNT PACK (PS 139798), MODEL/ITEM NUMBER UISH55V.

American Contract Systems Inc

FDA Devices Low Sep 3, 2025

C8-4v Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

VL13-5 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

S4-1 Lumify Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

S4-2 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

OMNI II TEE Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

C9-2 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

Akreos, SKU: AO60P0300. Akreos intraocular lenses

Bausch & Lomb Surgical, Inc.

FDA Devices Low Sep 3, 2025

3D9-3v Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

L18-5 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Brand Name: Atlantis IO FLO Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04S / 6802034 Product Description: The Atlantis intraoral feature locating object for suprastructures (IO FLO-S) is intended to support the prosthetic procedure with the aim of restoring chewing function in partial or complete edentulous patients, by enabling digital impression taking on implant or abutment level for all positions in the mouth of the patient or on the master model. Component: not a compone

Dentsply IH, Inc.

FDA Devices Moderate Sep 3, 2025

STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite analyzers, for the quantitative determination of the plasma levels of unfractionated (UFH) and low molecular weight (LMWH) heparins by measuring their anti-Xa activity on antithrombin in a competitive assay using a synthetic chromogenic substrate.

Diagnostica Stago, Inc.

FDA Devices Moderate Sep 3, 2025

AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) HEART PACK - 205947, MODEL/ITEM NUMBER ANCV78BC; 2) VASCULAR PACK - 232024, MODEL/ITEM NUMBER ANVA82AB; 3) OFF PUMP CABG PACK - 170316, MODEL/ITEM NUMBER BHOP48O; 4) OFF PUMP CABG PACK - 170316, MODEL/ITEM NUMBER BHOP48P; 5) PEDIATRIC OPEN HEART PACK - 170212, MODEL/ITEM NUMBER BHPH18F; 6) PEDIATRIC OPEN HEART PACK - 170212, MODEL/ITEM NUMBER BHPH18G; 7) CABG ACCESSORY PACK, MODEL/ITEM NUMBER HGCB98F; 8)

American Contract Systems Inc

FDA Devices Low Sep 3, 2025

D2cwc Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Orascoptic Superior Visualization Dragonfly Nose Pad Accessory Kit ( nose pad and screw) 1 pk and 20 pk.

Orascoptic Surgical Acuity

FDA Devices Low Sep 3, 2025

mL26-8 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) A-C SUPPLEMENT PACK - 205946, Model/Item Number ANCV67X; 2) KIDNEY PERFUSION PACK - 208439, Model/Item Number ANKP15AD; 3) LAPCHOLAPPY PACK, Model/Item Number FYLA38G; 4) CYSTO PACK, Model/Item Number HSCY13M; 5) PICC DRESSING CHANGE KIT, Model/Item Number HSDR10K; 6) MIDLINE CHANGE KIT, Model/Item Number HSMD20H; 7) SHOULDER ARTHOSCOPY PACK, Model/Item Number PDSA12D; 8) PDA LF SJW, Model/Item Number SW

American Contract Systems Inc

FDA Devices Low Sep 3, 2025

C6-3 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

eL18-4 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

STA Satellite. Product Code: All references. All software versions. The STA Satellite is a fully automated benchtop analyzer capable of simultaneously performing clotting, chromogenic, and immunologic assays.

Diagnostica Stago, Inc.

FDA Devices Low Sep 3, 2025

mC12-3 Transducer Probe

Philips Ultrasound, Inc

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.