PlainRecalls

2025 Recalls

6,168 recalls · Page 113 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 4 critical, 46 moderate, and 0 lower-severity recalls. The page references 19 distinct recalling firms operating in 4 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (43), CPSC (4), NHTSA (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, 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 5, 2025

HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN: M00553540

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN: M00553560

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT, Reorder number DYNDC3189; dressing change tray

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27001L, Uretero-Renoscope, 8 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27001K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The Sterile Percutaneous Refere…

Medtronic Navigation, Inc.

FDA Devices Moderate Feb 5, 2025

NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10

Zimmer, Inc.

FDA Devices Moderate Feb 5, 2025

HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553550

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

MEDLINE ARTERIAL LINE PACK, REF DYNJ65208B, medical convenience kit containing Infusion Catheter with Antimicrobial Heparin Coating.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27030KB, Pediatric Cysto-Urethroscope, NON STERILE, CE

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

CENTURION Infusion Catheter, 7F, 17cm (DO), Reorder MIC17F7; Infusion Catheter with Antimicrobial Heparin Coating.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 5, 2025

CyberKnife Treatment Delivery System, REF 0660000 The CyberKnife System may be labeled as CyberKnife M6TM or VSI TM Robotic Surgery System. The Cy…

Accuray Incorporated

FDA Devices Moderate Feb 5, 2025

AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553650

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27002KP, Pediatric Uretero-Renoscope 7.3 Fr., NON STERILE, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and Pyxis" MedStation 4000 ar…

CareFusion 303, Inc.

FDA Devices Moderate Feb 5, 2025

AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN: M00553670

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

Infinity Central Station. Model Number: MS26800 The Infinity CentralStation (ICS) is intended for centralized monitoring of adult, pediatric and n…

Draeger Medical Systems, Inc.

FDA Devices Moderate Feb 5, 2025

AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553680

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN: M00553640

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

ARTIS One Angiographic X-Ray System

SIEMENS MEDICAL SOLUTIONS USA, INC

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27000L,Uretero-Renoscope, 7 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

Medline procedure kits labeled as: 1) Port Access Kit, Reorder number CVI5130; 2) VANTEX 7FR 3L 20CM CVC STOCK+ BUNDLE US. Reorder number STCVC0…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27002K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN: M00553690

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

HemosIL Heparin Calibrators; Part Number: 0020300600; in vitro diagnostic

Instrumentation Laboratory

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27000K, Ureteroscope, 7 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27002L, Uretero-Renoscope, 9.5 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 10 x 25mm 5 degrees, Part #325-07102505, n…

Alphatec Spine, Inc.

FDA Devices Critical Feb 5, 2025

Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT, Item Number ART1185B; 2) ARTERIAL LINE BUNDLE, Item Number ART255; 3) ARTERI…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 5, 2025

Design Options COMBINED SPINAL/EPIDURAL TRAY- Intended for administration of analgesic/anesthetic agent to intrathecal space and epidural space for …

B. Braun Medical, Inc.

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27011K, Ureteroscope, 8 Fr., 6¿, 34cm, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN: M00553530

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C,D - Height 14 mm, Item Number 00-5994-022-14

Zimmer, Inc.

FDA Devices Moderate Feb 5, 2025

HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN: M00553570

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553520

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

AXIOS Stent and Delivery System 15mmx10mm UPN: M00553750

Boston Scientific Corporation

FDA Devices Moderate Feb 5, 2025

Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva", Model 1000 Model/Catalog Number: 1000 Software Version: NA Product Description: The Liv…

LivaNova USA, Inc.

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27010K, Ureteroscope, 7 Fr., 34 cm, NON STERILE, RxONLY, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

KARL STORZ - ENDOSKOPE, REF: 27011L, Uretero-Renoscope, 8 Fr., 6¿, 43cm, NON STERILE, RxONLY, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Feb 5, 2025

Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT, Reorder number DYNDC3188; surgery tray

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 5, 2025

muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate

Murata Vios, Inc.

FDA Devices Moderate Feb 5, 2025

Brand Name: SenTiva DUO" Product Name: VNS Therapy¿ SenTiva DUO", Model 1000-D Model/Catalog Number: 1000-D Software Version: NA Product Descript…

LivaNova USA, Inc.

FDA Devices Moderate Feb 5, 2025

AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN: M00553660

Boston Scientific Corporation

NHTSA Critical Feb 5, 2025

HONDA 2025: SEAT BELTS:REAR/OTHER

HONDA

NHTSA Critical Jan 31, 2025

FORD,LINCOLN 2025: ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL

FORD,LINCOLN

NHTSA Critical Jan 31, 2025

FORD,LINCOLN 2020-2022: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

FORD,LINCOLN

CPSC Moderate Jan 30, 2025

AliExpress Recalls Multi Styler Hair Dryers Due to Electrocution or Shock Hazards; Sold on AliExpress.com

Super Appliance Store, of China

CPSC Moderate Jan 30, 2025

AMX Global Recalls Portable Folding Stadium Seats Due to Fall and Injury Hazards

CPSC Moderate Jan 30, 2025

Cabinet Health Recalls 4 oz. Refillable Medicine Bottles Due to Failure to Retain Child-Resistance; Risk of Child Poisoning

Cabinet Health Inc., of Washington, D.C.

CPSC Moderate Jan 30, 2025

Cozchique Tebbis, and Beeziac Girls Pajamas Recalled Due to Burn Hazard; Violation of Federal Flammability Regulations; Sold Exclusively on Amazon by…

Tupop E-Commerce Co. Ltd., of China

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.