PlainRecalls

2025 Recalls

6,168 recalls · Page 59 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 7 critical, 43 moderate, and 0 lower-severity recalls. The page references 29 distinct recalling firms operating in 4 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (36), NHTSA (8), FDA Drug (5), 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 Drug Moderate Jul 30, 2025

Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd. Indore SEZ, Pith…

Cipla USA, Inc.

FDA Drug Moderate Jul 30, 2025

Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 078…

Imprimis NJOF, LLC

FDA Drug Moderate Jul 30, 2025

clomiPRAMINE Hydrochloride Capsules USP 25 mg, 100 count bottles, 5801 Pelican Bay Boulevard, Suite 500, Naples, Florida 34108, NDC# 68180-492-01

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Jul 30, 2025

BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Drug Moderate Jul 30, 2025

PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jul 30, 2025

Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B; 2) BLOOD CULTURE KI…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 30, 2025

Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application, Software M…

Medtronic, Inc.

FDA Devices Moderate Jul 30, 2025

Estrone RIA, REF: DSL8700. Estrone RIA is an IVD used for the quantitative measurement of estrone in human serum and plasma.

Beckman Coulter Inc.

FDA Devices Moderate Jul 30, 2025

Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: IV START KIT LAB DRAW-SH, REF CDS860014P

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 30, 2025

Stryker, StrykeFlow REF: 0250070520 / 2, Disposable Suction/Irrigator with Disposable Tip

Stryker Corporation

FDA Devices Moderate Jul 30, 2025

Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.

Olympus Corporation of the Americas

FDA Devices Moderate Jul 30, 2025

Tubing for Male Connector 194, Ellik Evacuator. Model Number: 190-4. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI El…

Olympus Corporation of the Americas

FDA Devices Moderate Jul 30, 2025

Biofinity XR Toric Contact Lens

CooperVision, Inc.

FDA Devices Moderate Jul 30, 2025

SIGNA Architect

GE Medical Systems, LLC

FDA Devices Moderate Jul 30, 2025

Medtronic CareLink SmartSync Device Manager, Model Number 24967A with the following software components: 1. Cobalt Crome application, Software Mod…

Medtronic, Inc.

FDA Devices Moderate Jul 30, 2025

Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: C-SECTION PREP, REF DYNJ32702B

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 30, 2025

Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: LABOR TRIAGE KIT, REF DYKM1564

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 30, 2025

Cone with Male Tubing, Non-Locking, Ellik Evacuator. Model Number: 191-NRS. The Ellik Evacuator and adapter accessories are compatible with Gyrus…

Olympus Corporation of the Americas

FDA Devices Moderate Jul 30, 2025

Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard electroencephalograph

Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

FDA Devices Moderate Jul 30, 2025

SIGNA Architect AIR

GE Medical Systems, LLC

FDA Devices Moderate Jul 30, 2025

Glass Body For 194 Ellik Evacuator. Model Number: 190A. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elit…

Olympus Corporation of the Americas

FDA Devices Moderate Jul 30, 2025

Ellik Latex Bulb, Ellik Evacuator. Model Number: 194-2. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elit…

Olympus Corporation of the Americas

FDA Devices Moderate Jul 30, 2025

Azurion 7 M20. Fluoroscopic X-Ray System.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jul 30, 2025

Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV. Endosee System Convenience Kit with IV Tube.

CooperSurgical, Inc.

FDA Devices Moderate Jul 30, 2025

Bridge to Life EasiSlush, (Sodium Chloride Solution for Sterile Slush Preparation) (0.9% Sodium Chloride Irrigation, USP), Part Number REF BTLE-1250

Bridge to Life Ltd

FDA Devices Moderate Jul 30, 2025

Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 Model/Catalog Number: 952-28-40E Softwa…

Encore Medical, LP

FDA Devices Moderate Jul 30, 2025

BD COR System Software. Model Number: 444829.

Becton Dickinson & Co.

FDA Devices Moderate Jul 30, 2025

Portable X-ray system

DIGIMED CO., LTD

FDA Devices Moderate Jul 30, 2025

SIGNA PET/MR

GE Medical Systems, LLC

FDA Devices Moderate Jul 30, 2025

Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System Convenience Kit

CooperSurgical, Inc.

FDA Devices Moderate Jul 30, 2025

Ellik Evacuator Adapter, Locking. Model Number: 190-NRS. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Eli…

Olympus Corporation of the Americas

FDA Devices Moderate Jul 30, 2025

Green Silicone Seal for Accessories, Reusable Silicone Seal 0 - 7 FR. Model Number: CS-G7. The reusable silicone seals fit over the biopsy port …

Olympus Corporation of the Americas

FDA Devices Moderate Jul 30, 2025

Bodor's I series laser cutting machine.

Jinan Bodor Cnc Machine Co Ltd

FDA Devices Moderate Jul 30, 2025

Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42 Model/Catalog Number: 952-28-42F Softwa…

Encore Medical, LP

FDA Devices Moderate Jul 30, 2025

HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and sonohysterography procedures.

CooperSurgical, Inc.

FDA Devices Moderate Jul 30, 2025

Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N, 10005941-SG, DS10005941, 10005941J…

Covidien

FDA Devices Moderate Jul 30, 2025

ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL

Johnson & Johnson Vision Care, Inc.

FDA Devices Moderate Jul 30, 2025

Discovery MR750w 3.0T

GE Medical Systems, LLC

FDA Devices Moderate Jul 30, 2025

Biofinity Toric Multifocal Contact Lens

CooperVision, Inc.

FDA Devices Moderate Jul 30, 2025

Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip

Stryker Corporation

FDA Devices Moderate Jul 30, 2025

Blue Silicone, Reusable Silicone Seal 6 - 12 FR. Model Number: CS-B612. The reusable silicone seals fit over the biopsy port of endoscopes to s…

Olympus Corporation of the Americas

NHTSA Critical Jul 28, 2025

KIA 2023-2025: STRUCTURE:EXTERIOR TRIM

KIA

NHTSA Critical Jul 28, 2025

KIA 2023-2025: STRUCTURE:BODY:ROOF AND PILLARS

KIA

NHTSA Critical Jul 28, 2025

TESLA 2026: ELECTRICAL SYSTEM:HORN

TESLA

NHTSA Critical Jul 25, 2025

FORD 2025: SEAT BELTS:FRONT:WARNING LIGHT/DEVICES

FORD

NHTSA Critical Jul 25, 2025

FORD,LINCOLN 2025: SERVICE BRAKES, HYDRAULIC:POWER ASSIST:ELECTRIC:CONTROL MODULE:SOFTWARE

FORD,LINCOLN

NHTSA Critical Jul 25, 2025

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

MERCEDES-BENZ

NHTSA Moderate Jul 25, 2025

LINCOLN 2025: VISIBILITY:POWER WINDOW DEVICES AND CONTROLS

LINCOLN

NHTSA Critical Jul 25, 2025

BMW 2025: COMMUNICATION: AUTO CRASH NOTIFICATION

BMW

CPSC Moderate Jul 24, 2025

Aiho Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard; Sold on Walmart.com by Aiho

Shenzhen Yiqun Technology Co. Ltd. dba Aiho Inc., 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 July 2026.