2025 Recalls

Compiled from official public sources by the editorial team. · Updated July 2026

6,168 recalls · Page 3 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 14 critical, 34 moderate, and 2 lower-severity recalls. The page references 29 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 (30), NHTSA (10), CPSC (10), 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.

← 2024 2026 →

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…

GE Medical Systems China Co., Ltd.

2025 Recalls

2025 Recall Year Insight

Cardiosave Rescue

GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1 REF 1012…

Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number: 502-103 - Calf Implant style 1 size 3 UDI-DI code: B490502103 5…

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

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

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: B490401…

Cardiosave Hybrid

Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54549-20-PK Software Version: N/A Product D…

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

5008X CAREsystem +CLiC +CDX;

Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-12-SG Software Version: N/A Produc…

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 Spe…

Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-18-PK Software Version: N/A Product D…

Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant Model/Catalog Numbers: 600-601 - Silicone Carving Implant Style 6 Si…

GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 750 A1, REF 1012-9750-000; Carestation 750 A2, REF 1012…

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

Zimmer Dermatome AN, Model/Catalog Number: 88710100

Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog Numbers: 400-0101 Chin Implant style 1 size 1 UDI-DI code: B490400101 4…

Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-12-PK Product Description: Chest tube …

Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012; Navigation Straight Bone Probe, REF…

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

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

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

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

Intelerad InteleShare software, with ProViewer component

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…

Brand Name: AART Gluteal Implant Product Name: Gluteal Implant Model/Catalog Numbers: 501-101 - Gluteal Implant style 1 size 1 UDI-DI code: B4905…

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

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

Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-18-SG Software Version: N/A Produc…

NISSAN 2026: TIRES:TEMPORARY/EMERGENCY SPARE TIRE

HONDA 2024: ELECTRICAL SYSTEM:WIRING

VOLVO 2021-2025: BACK OVER PREVENTION:SOFTWARE

BMW 2025: ELECTRICAL SYSTEM:PROPULSION SYSTEM: CABLES

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

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

AUDI 2025: SEAT BELTS:REAR/OTHER:RETRACTOR

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

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

HYUNDAI 2022-2024: TRAILER HITCHES

17 Stories Furniture 18-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Stan…

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

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

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

Currey & Company Recalls Electra Chandeliers Due to Impact Injury Hazard

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

Furnulem 8-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violate Mandatory Standard for Clothing Stor…

JOKOSIS Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violates Mandatory Standar…

KKL Fabric 9-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clo…

Meaicezli Play Purse Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazo…

Nearby Recall Years

Data Sources