PlainRecalls

2025 Recalls

5,015 recalls · Page 42 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 9 critical, 39 moderate, and 2 lower-severity recalls. The page references 24 distinct recalling firms operating in 6 distinct product categories, with 48 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (37), CPSC (8), FDA Food (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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Low Aug 20, 2025

Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10

Diversatek Healthcare

FDA Devices Moderate Aug 20, 2025

Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S Software Version: Not Applica…

SPINEART SA

FDA Devices Critical Aug 20, 2025

Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS

Baxter Healthcare Corporation

FDA Devices Moderate Aug 20, 2025

GE SIGNA Premier XT (China Only), Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Catheter Kit Model/Catalog Number: IMU7F-40, IMU7F-35, IMU7F-30, IMU7F-25, and IMU7F-2…

Insightra Medical Inc

FDA Devices Moderate Aug 20, 2025

Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number: 341-16-704 Product Descriptio…

Encore Medical, LP

FDA Devices Moderate Aug 20, 2025

Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/CS Model…

Carefree Surgical Specialties

FDA Devices Moderate Aug 20, 2025

GE Signa Voyager, Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 7R 16MM, VE Model/Catalog Number: 342-16-707 Product Descriptio…

Encore Medical, LP

FDA Devices Moderate Aug 20, 2025

Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Roll Gauze + Tail Medium 4 Long X-Ray Detectable 5pk 25pk/CS Ro…

Carefree Surgical Specialties

FDA Devices Critical Aug 20, 2025

Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Resuscitator w/Mercury Filter, …

Ambu Inc.

FDA Devices Moderate Aug 20, 2025

GE Discovery MR750 3.0T, Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

GE Discovery MR450 1.5T, Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

Sparrow Ascent Patient Controller, REF's: 11-110-K, 11-310-K, 11-320-K, 11-321-K, 11-310-K-28, 11-320-K-28, 11-321-K-28

Spark Biomedical Inc

FDA Devices Moderate Aug 20, 2025

GE SIGNA Hero XT (China Only), Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

Bartels ELISA Legionella Urinary Antigen. Model Number: B1029-440. In Vitro Diagnostic test kit for the presumptive diagnosis of past or current L…

Trinity Biotech USA

FDA Devices Moderate Aug 20, 2025

HemosIL LMW Heparin Controls; Part Number: 0020300200;

Instrumentation Laboratory

FDA Devices Critical Aug 20, 2025

DreamStation Auto BiPAP. Non-Continuous Ventilator.

Philips Respironics, Inc.

FDA Devices Moderate Aug 20, 2025

FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401

Boston Scientific Corporation

FDA Devices Critical Aug 20, 2025

DreamStation Auto. Non-Continuous Ventilator.

Philips Respironics, Inc.

FDA Devices Moderate Aug 20, 2025

GE SIGNA Artist Evo, Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Low Aug 20, 2025

Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI 4HH/169-112, BD PYXIS MEDBANK …

CareFusion 303, Inc.

FDA Devices Moderate Aug 20, 2025

Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/CS Model…

Carefree Surgical Specialties

FDA Devices Moderate Aug 20, 2025

Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 65 40-S Software Version: Not Applica…

SPINEART SA

FDA Devices Moderate Aug 20, 2025

GE SIGNA PET/MR AIR (China Only), Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Critical Aug 20, 2025

Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 Software Version: N/A Product Description: The …

Thoratec LLC

FDA Devices Moderate Aug 20, 2025

GE SIGNA PET/MR, Tomographic Imager Combining Emission Computed Tomography with Nuclear Magnetic Resonance

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

Prosthesis Head B, 28 mm, 7 mm neck length. Item Number: 198-828/04.

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 20, 2025

GE SIGNA Hero Elite (China Only), Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

GE SIGNA PET/MR AIR Plus (China Only), Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

Custom Manifold Kit: REF: K09-02239C, K09-02249UP, K09-09110B, K09-10294A, K09-11227A, K09-11456B, K09-12123B, K09-13342AP, K09-13391BP, K09-13548, …

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 20, 2025

GE SIGNA Hero MAX (China Only), Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 20, 2025

Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray Detectable 5pk 25pk/CS Roll Gauzes M…

Carefree Surgical Specialties

FDA Devices Moderate Aug 20, 2025

GE SIGNA Architect AIR (China Only), Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Critical Aug 20, 2025

DreamStation Auto CPAP. Non-Continuous Ventilator.

Philips Respironics, Inc.

FDA Devices Moderate Aug 20, 2025

Custom Tubing Kit: REF: K04-00417, K04-00963, K04-01029

Merit Medical Systems, Inc.

NHTSA Critical Aug 20, 2025

MERCEDES-BENZ 2023-2026: STEERING:CRITICAL FASTENERS

MERCEDES-BENZ

CPSC Moderate Aug 14, 2025

Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violates the Small Ball Ban; Sold on Shein by STWUQIKONG

Shantou Jinping District Wuqikong Daily Necessities Store, dba STWUQIKONG, of China

CPSC Moderate Aug 14, 2025

Drinkmate Recalls 1-Liter Carbonation Bottles Due to Serious Impact and Laceration Hazards

CPSC Moderate Aug 14, 2025

Empower Brands Recalls Remington Hair Dryers Due to Risk of Serious Injury or Death from Electrocution and Shock Hazards

CPSC Moderate Aug 14, 2025

ESR HaloLock Wireless Power Banks Recalled Due to Fire and Burn Hazards; Distributed by Waymeet

Waymeet Limited, of Hong Kong

CPSC Moderate Aug 14, 2025

Firefly Fuel Recalls Firefly Safe & Green 32 oz. Fuel Bottles Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Multi…

Firefly Fuels Inc., of Sarasota, Florida

CPSC Moderate Aug 14, 2025

Synergy Housewares Recalls Wolfgang Puck Petite Tea Kettles Due to Burn Hazard; Sold on HSN

CPSC Moderate Aug 14, 2025

Viewrail Recalls Electronic LED Modules used with Floating Stairs and Rails Due to Fire Hazard

CPSC Moderate Aug 14, 2025

Werner Recalls 20' and 24' Multi-Max Pro Multi-Purpose Ladders Due to Fall Hazard

NHTSA Critical Aug 14, 2025

JEEP 2024-2025: TIRES:PRESSURE MONITORING AND REGULATING SYSTEMS

JEEP

FDA Food Critical Aug 13, 2025

Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.35OZ (10g) STRAWBERRY POUCHES 5-0.42OZ (12g) BANANA POUCHES 5-0.25 OZ (10g) APPLE POUCHES …

Doehler North America, Inc.

FDA Food Moderate Aug 13, 2025

Twister Fruit Punch, 59 FL OZ (1.84 QT) 1.75 L, packaged in a paper carton, UPC: 048500021231

Dollar General Corporation

FDA Food Moderate Aug 13, 2025

Milo's Famous Sweet Tea, 128 FL OZ (1 GAL) 3.78 L, packaged in a plastic jug, UPC: 091475511009

Dollar General Corporation

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2025