PlainRecalls

2025 Recalls

6,168 recalls · Page 111 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 8 critical, 42 moderate, and 0 lower-severity recalls. The page references 27 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 Moderate Feb 12, 2025

IntelliVue Patient Monitor MX550. Model Number: 866066

Philips North America Llc

FDA Devices Moderate Feb 12, 2025

Definium 656HD & Discovery XR656HD (GTINs: 00840682138598, 00195278840226, 00840682136709). X-Ray imaging system.

GE Medical Systems, LLC

FDA Devices Moderate Feb 12, 2025

The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of the Rapid fFN Specimen Collection kit (PN: 71738-001). The Collection Tube (…

Hologic, Inc.

FDA Devices Critical Feb 12, 2025

regard Item Number: 830106006, LD01114F - Newborn Kit containing the component Neo-Tee Resuscitator. Convenience kit to be used in Labor and Delivery.

ROi CPS LLC

FDA Devices Critical Feb 12, 2025

Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Indicated for use in a hospital and in outpatient care environments for the controlled adm…

Fresenius Kabi USA, LLC

FDA Devices Moderate Feb 12, 2025

Lev5, REF CT1587B, 50 Susceptibility discs Levofloxacin 5 ug, IVD, CE 2797

Oxoid Limited

FDA Devices Moderate Feb 12, 2025

IntelliVue Patient Monitor MX500. Model Number: 866064

Philips North America Llc

FDA Devices Moderate Feb 12, 2025

Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

Allura CV20 System Code: 722031

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

ETHIBOND EXCEL Polyester Suture, REF: 6664H, X425H, X872H, EH7491H. Not sold in US

Ethicon, LLC

FDA Devices Moderate Feb 12, 2025

Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

Discovery XR656 HD. X-Ray imaging system.

GE Medical Systems, LLC

FDA Devices Moderate Feb 12, 2025

Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK AP120253PK AP120313PK AP125213PK AP125253PK AP125313PK AP135213PK …

US Endodontics, LLC

FDA Devices Moderate Feb 12, 2025

AlluraXperFD20/10 System Code: (1) 722029

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137; in-vitro diagnostic instrument

Beckman Coulter, Inc.

FDA Devices Moderate Feb 12, 2025

Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282 System Code: (1) 722078 (2) 722223 (3) 722233

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

AlluraXperFD20/15 System Code: (1) 722058

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

Access PCT Reagent Pack, Catalog Number C53987, when used on Access 2 and UniCel Dxl Immunoassay Systems

Beckman Coulter Inc.

FDA Devices Moderate Feb 12, 2025

Azurion 5 M12 System Code: (1) 722227 (2) 722231

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each), Model: C-CA-23, Item: 33516;

New Medical Technologies Gmbh

FDA Devices Moderate Feb 12, 2025

Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Infuser RI-2. Designed to be used in general operation in hospital or alternate ca…

Belmont Instrument LLC

FDA Devices Moderate Feb 12, 2025

Allura Xper FD20/20 System Code: (1) 722038

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

. Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Biocare N1 TiUltra TCC RP 4.0x11mm . Nobel Biocare N1 TiUltra TCC RP 4.0x13mm Nobel Biocare N1…

Nobel Biocare

FDA Devices Moderate Feb 12, 2025

NeiMed NasoGel for DRY NOSES UDI-DI/UPC code: 00705928045309 SKU GSP30-2R-48-ENU-USL GSP30-0R-96-ENU-USL GSP30-ARA-INTL GSP30-SWE-INTL GSP30-ENG-INT …

Neilmed Pharmaceuticals Inc

FDA Devices Moderate Feb 12, 2025

Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

Discovery XR656HD. X-Ray imaging system.

GE Medical Systems, LLC

FDA Devices Moderate Feb 12, 2025

Temporary Titanium Abutments

DDS Lab

FDA Devices Moderate Feb 12, 2025

IntelliBridge EC10 Module. Model Number: 865115

Philips North America Llc

FDA Devices Moderate Feb 12, 2025

AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

PERMA-HAND Silk Suture, REF: K872H, W723H, 623H, K833H; Perma-hand Silk Suture is indicated for use in general soft tissue approximation and/or ligat…

Ethicon, LLC

FDA Devices Moderate Feb 12, 2025

Allura Xper FD10C System Code: (1) 722001

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 12, 2025

LIFEPAK 35 ECG cable REF 11111-000041

Physio-Control, Inc.

FDA Devices Moderate Feb 12, 2025

Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6., Catalog Number BQ716341. Product usage for automated pipetting, diluting,…

Sysmex America, Inc.

NHTSA Critical Feb 12, 2025

AUDI,VOLKSWAGEN 2022-2025: BACK OVER PREVENTION:SOFTWARE

AUDI,VOLKSWAGEN

NHTSA Critical Feb 12, 2025

VOLKSWAGEN 2025: POWER TRAIN:AUTOMATIC TRANSMISSION

VOLKSWAGEN

NHTSA Critical Feb 12, 2025

AUDI 2021-2024: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY

AUDI

NHTSA Critical Feb 12, 2025

PORSCHE 2023: SEAT BELTS: REAR/OTHER:BUCKLE ASSEMBLY

PORSCHE

NHTSA Critical Feb 7, 2025

VOLVO 2025: EXTERIOR LIGHTING:HEADLIGHTS:CONCEALMENT DEVICES

VOLVO

NHTSA Critical Feb 7, 2025

MERCEDES-BENZ 2022-2024: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY

MERCEDES-BENZ

CPSC Moderate Feb 6, 2025

Ariens Recalls Snow Throwers Due to Laceration Hazard

Ariens Company, of Brillion, Wisconsin

CPSC Moderate Feb 6, 2025

Doosan Bobcat North America Recalls Bobcat & Steiner AirFX Finish Mower Deck Attachments Due to Crush Hazard

Doosan Bobcat North America, of West Fargo, North Dakota

CPSC Moderate Feb 6, 2025

Jazwares Recalls America's Got Talent Microphones with Lithium-Ion Batteries Due to Fire Hazard

CPSC Moderate Feb 6, 2025

LG Recalls Electric Ranges Due to Fire Hazard

LG Electronics Inc., of South Korea

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.