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 16 critical, 32 moderate, and 2 lower-severity recalls. The page references 27 distinct recalling firms operating in 5 distinct product categories, with 40 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (31), NHTSA (10), CPSC (7), 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 Moderate Dec 24, 2025

Halyard, EP LAB PK. Catalog Number: ESJH009-03.

AVID Medical, Inc.

FDA Devices Low Dec 24, 2025

Cardiosave Rescue

Datascope Corp.

FDA Devices Critical Dec 24, 2025

GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1 REF 1012-9620-000; Carestation 620 A1, REF 1012-9620-200; Carestation 620 A1, REF 1012-9620-202; Carestation 620 SE A1, REF 1012-9620-212; Carestation 630 A1, REF 1012-9650-222; Carestation 650 A1, REF 1012-9650-000; Carestation 650 A1, REF 1012-9650-200; Carestation 650 A1, REF 1012-9650-202; Carestation 650 SE A1, REF 1012-9650-212; Care

GE Medical Systems China Co., Ltd.

FDA Devices Moderate Dec 24, 2025

Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number: 502-103 - Calf Implant style 1 size 3 UDI-DI code: B490502103 502-104 - Calf Implant style 1 size 4 UDI-DI code: B490502104 502-105 - Calf Implant style 1 size 5 UDI-DI code: B490502105 502-106 - Calf Implant style 1 size 6 UDI-DI code: B490502106 502-201 - Calf Implant style 2 size 1 UDI-DI code: B490502201 502-303 - Calf Implant style 3 size 3 UDI-DI code: B490502303 502-304 - Calf Implant

DSAART LLC

FDA Devices Moderate Dec 24, 2025

Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.

AVID Medical, Inc.

FDA Devices Moderate Dec 24, 2025

Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.

AVID Medical, Inc.

FDA Devices Moderate Dec 24, 2025

Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog Number: 401-202-5 Malar Implant style 2 size 2 left UDI-DI code: B4904012025 401-202-6 Malar Implant style 2 size 2 right UDI-DI code: B4904012026

DSAART LLC

FDA Devices Low Dec 24, 2025

Cardiosave Hybrid

Datascope Corp.

FDA Devices Moderate Dec 24, 2025

Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54549-20-PK Software Version: N/A Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied with a procedure pack to allow percutaneous insertion, supplied with connectors to allow attachment to chest drain bottle devices. Component: N/A

Rocket Medical Plc

FDA Devices Critical Dec 24, 2025

Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Software for the controlled administration of fluids to patients.

Fresenius Kabi USA, LLC

FDA Devices Moderate Dec 24, 2025

5008X CAREsystem +CLiC +CDX;

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Dec 24, 2025

Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-12-SG Software Version: N/A Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied with a procedure pack to allow percutaneous insertion, supplied with connectors to allow attachment to chest drain bottle devices. Component: N/A

Rocket Medical Plc

FDA Devices Moderate Dec 24, 2025

1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with Copan s WASP (Walk-Away Specimen Processor for Microbiology) System

Copan Italia

FDA Devices Moderate Dec 24, 2025

Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-18-PK Software Version: N/A Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied with a procedure pack to allow percutaneous insertion, supplied with connectors to allow attachment to chest drain bottle devices. Component: N/A

Rocket Medical Plc

FDA Devices Moderate Dec 24, 2025

Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant Model/Catalog Numbers: 600-601 - Silicone Carving Implant Style 6 Size 1 UDI-DI code: B490600601 600-602 - Silicone Carving Implant Style 6 Size 2 UDI-DI code: B490600602 600-601-9 - Silicone Carving Implant Style 6 Size 1 with Suture Tabs UDI-DI code: B4906006019 600-603-9 - Silicone Carving Implant Style 6 Size 3 with Suture Tabs UDI-DI code: B4906006039 600-604-9 - Silicone Carving Implant Style 6 Size 4 with

DSAART LLC

FDA Devices Critical Dec 24, 2025

GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 750 A1, REF 1012-9750-000; Carestation 750 A2, REF 1012-9750-002; Carestation 750c A1, REF 1012-9755-000; Products for which affected PMB can be used as a spare part: Carestation 750c A2, REF 1012-9755-002

GE Medical Systems China Co., Ltd.

FDA Devices Moderate Dec 24, 2025

Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10

Cepheid

FDA Devices Moderate Dec 24, 2025

Zimmer Dermatome AN, Model/Catalog Number: 88710100

Zimmer Surgical Inc

FDA Devices Moderate Dec 24, 2025

Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog Numbers: 400-0101 Chin Implant style 1 size 1 UDI-DI code: B490400101 400-0103 Chin Implant style 1 size 3 UDI-DI code: B490400103 400-0104 Chin Implant style 1 size 4 UDI-DI code: B490400104 400-0201 Chin Implant style 2 size 1 UDI-DI code: B490400201 400-0202 Chin Implant style 2 size 2 UDI-DI code: B490400202 400-0301 Chin Implant style 3 size 1 UDI-DI code: B49044301 400-0302 Chin Implant style

DSAART LLC

FDA Devices Moderate Dec 24, 2025

Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-12-PK Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied with a procedure pack to allow percutaneous insertion, supplied with connectors to allow attachment to chest drain bottle devices. Component: N/A

Rocket Medical Plc

FDA Devices Moderate Dec 24, 2025

Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012; Navigation Straight Bone Probe, REF: PC2-400013; Navigation, 3.5mm Drill, REF: PC2-400135; Navigation, 4.0mm Drill, REF: PC2-400140; Navigation, 4.5mm Drill, PC2-400145; Navigation, 5.5mm Drill, REF: PC2-400155; Navigation, 3.5mm Tap, REF: PC2-400235; Navigation, 4.0mm Tap, REF: PC2-400240; Navigation, 4.5mm Tap, REF: PC2-400245; Navigation, 4.5mm Dual Lead Tap, REF: PC2-400345; Navi

SEASPINE ORTHOPEDICS CORPORATION

FDA Devices Moderate Dec 24, 2025

InPen App, Model/CFN Number: MMT-8061 (Android Users)

Medtronic MiniMed, Inc.

FDA Devices Moderate Dec 24, 2025

SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000

Medline Industries, LP

FDA Devices Moderate Dec 24, 2025

1ml of DTT in liquid phase, in PET tube with capture cap, in bulk

Copan Italia

FDA Devices Moderate Dec 24, 2025

FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048

Medline Industries, LP

FDA Devices Moderate Dec 24, 2025

Intelerad InteleShare software, with ProViewer component

DICOM Grid, Inc.

FDA Devices Moderate Dec 24, 2025

Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/Catalog Number: 500-106-5 Pectoral Implant style 1 size 6 left UDI-DI code: B4905001065 500-106-6 Pectoral Implant style 1 size 6 right UDI-DI code: B4905001066 500-200-5 Pectoral Implant style 2 size 0 left UDI-DI code: B4950020205 500-200-6 500-201-5 500-201-6 500-202-5 500-202-6 500-403-5 500-403-6

DSAART LLC

FDA Devices Moderate Dec 24, 2025

Brand Name: AART Gluteal Implant Product Name: Gluteal Implant Model/Catalog Numbers: 501-101 - Gluteal Implant style 1 size 1 UDI-DI code: B490501101 501-103 - Gluteal Implant style 1 size 3 UDI-DI code: B490501103 501-101 UDI-DI code: B490501101 501-103 - Gluteal Implant style 1 size 3 UDI-DI code: B490501103 501-105 - Gluteal Implant style 1 size 5 UDI-DI code: B490501105 501-206 - Gluteal Implant style 2 size 6 UDI-DI code: B490501206 501-301 - Gluteal Implant styl

DSAART LLC

FDA Devices Moderate Dec 24, 2025

Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.

AVID Medical, Inc.

FDA Devices Critical Dec 24, 2025

GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replaceable Unit (FRU), 2076139-001-S

GE Medical Systems China Co., Ltd.

FDA Devices Moderate Dec 24, 2025

Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-18-SG Software Version: N/A Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied with a procedure pack to allow percutaneous insertion, supplied with connectors to allow attachment to chest drain bottle devices.

Rocket Medical Plc

NHTSA No agency class Dec 23, 2025

NISSAN 2026: TIRES:TEMPORARY/EMERGENCY SPARE TIRE

NISSAN

NHTSA No agency class Dec 23, 2025

HONDA 2024: ELECTRICAL SYSTEM:WIRING

HONDA

NHTSA No agency class Dec 23, 2025

VOLVO 2021-2025: BACK OVER PREVENTION:SOFTWARE

VOLVO

NHTSA No agency class Dec 23, 2025

BMW 2025: ELECTRICAL SYSTEM:PROPULSION SYSTEM: CABLES

BMW

NHTSA No agency class Dec 21, 2025

LAMBORGHINI 2022-2023: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

LAMBORGHINI

NHTSA No agency class Dec 19, 2025

AUDI 2019-2026: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

AUDI

NHTSA No agency class Dec 19, 2025

AUDI 2025: SEAT BELTS:REAR/OTHER:RETRACTOR

AUDI

NHTSA No agency class Dec 19, 2025

PORSCHE 2019-2025: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

PORSCHE

NHTSA No agency class Dec 19, 2025

MERCEDES-BENZ 2022-2023: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY

MERCEDES-BENZ

NHTSA No agency class Dec 19, 2025

HYUNDAI 2022-2024: TRAILER HITCHES

HYUNDAI

USDA FSIS Critical Dec 19, 2025

Olympia Provisions Recalls Ready-to-Eat Holiday Kielbasa Sausage Products Due to Possible Foreign Matter Contamination

Olympia Provisions

USDA FSIS Critical Dec 19, 2025

Maître Saladier Inc. Recalls Lorraine Quiche Products Imported Without Benefit of Import Reinspection

CPSC No agency class Dec 18, 2025

17 Stories Furniture 18-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Imported by Shenzhen Jinhongzhen Technology Co

Jiangsu Quanronghe Smart Home Co., Ltd., of China

CPSC No agency class Dec 18, 2025

Amp Fit Recalls AMP Smart Fitness Machines Due to Laceration and Serious Injury Hazard

CPSC No agency class Dec 18, 2025

ANNQUAN Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Fire; Sold on Amazon by Hefei Juyuan Sporting Development

Hefei Juyuan Sporting Development Co., Ltd., of China

CPSC No agency class Dec 18, 2025

Blue Wave Recalls Above-Ground Pools 48 Inches and Taller Due to Drowning Hazard

CPSC No agency class Dec 18, 2025

Currey & Company Recalls Electra Chandeliers Due to Impact Injury Hazard

CPSC No agency class Dec 18, 2025

Feel The Beard Recalls Minoxidil Beard Growth Serum Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging

CPSC No agency class Dec 18, 2025

Furnulem 8-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Furnulem

Shanghai Taiye Furniture Co., Ltd., dba Furnulem, 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: 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.