PlainRecalls

2025 Recalls

5,015 recalls · Page 100 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, 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 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 6 critical, 44 moderate, and 0 lower-severity recalls. The page references 28 distinct recalling firms operating in 6 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (27), FDA Drug (12), CPSC (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 Devices Moderate Jan 8, 2025

Ivalon Anatomical Nasal Packing with Airway Tube and String, 8.0 cm x 1.5cmx 3.0 cm- Intended To Be Used During Ophthalmic Surgical Procedures For Fl…

Carwild Corporation

FDA Devices Moderate Jan 8, 2025

Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jan 8, 2025

Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX

Baxter Healthcare Corporation

CPSC Moderate Jan 8, 2025

Multi-Purpose Children's Helmets Recalled Due to Risk of Head Injury; Violation of Federal Regulations for Bicycle Helmets; Sold Exclusively on Amazo…

CPSC Moderate Jan 8, 2025

SIG SAUER Recalls ROMEO5 Red Dot Firearm Sights Due to Ingestion Hazard; Violations of Reese's Law Federal Safety Regulations for Consumer Products w…

CPSC Moderate Jan 2, 2025

Euqee Wintergreen Essential Oils Recalled Due to Risk of Poisoning; Violation of the Poison Prevention Packaging Act; Sold Exclusively on Amazon.com …

DingLinWangLuoKeJiGuang ZhouYouXianGongSi, dba DLWL-US, of China

CPSC Moderate Jan 2, 2025

Kawasaki Motors USA Recalls John Deere ZTrak Zero Turn Mowers with Kawasaki Engines Due to Fire and Burn Hazards

Kawasaki Motors Manufacturing Corp. U.S.A. (engine manufacturer), of Maryville, Missouri

CPSC Moderate Jan 2, 2025

Yaomiao Children's Jewelry Sets Recalled Due to Risk of Lead and Cadmium Poisoning; Violations of the Federal Lead Content Ban and Federal Hazardous …

Wuhannuoyunxindianzikejiyouxiangongsi, (dba LordRoads), of China

NHTSA Critical Jan 2, 2025

ASTON MARTIN 2025: BACK OVER PREVENTION:DISPLAY FUNCTION

ASTON MARTIN

FDA Food Moderate Jan 1, 2025

BORSARI Food Company Incorporated; BLOODY MARY MIX ; 32 FL. OZ; INGREDIENTS: Tomato juice, corn syrup, non-fat milk solids, orange juice, lemon juice…

Borsari Food Company Inc

FDA Food Critical Jan 1, 2025

Kirkland Signature ORGANIC EGGS PASTURE-RAISED 24 EGGS, GRADE A LARGE, NET WEIGHT 48OZ (3 LB) 1.36 kg, UPC 0 96619 10680 6, DISTRIBUTED BY: COSTCO WH…

Handsome Brook Farms, LLC

FDA Food Critical Jan 1, 2025

Cucumber Diced Greek Cut (1/8"x1/8"x1"), 360# Drum with poly liner item C0376, 30# Box with poly liner item C0369. Cucumber Diced Regular Cut (1/8"x1…

E-Z SPUDS INC

FDA Food Critical Jan 1, 2025

Raw cucumbers packaged in cardboard boxes or plastic boxes (RPC) with "SunFed", "Vegetables", or "Agrotato" labeling. 1 1/9 BU CAS Super Slicer Cuc…

SunFed Produce, Inc.

FDA Food Moderate Jan 1, 2025

ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch

Zoe US, Inc.

FDA Drug Moderate Jan 1, 2025

Duloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, 90-count bottles (NDC 51991-747-90) Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (…

Breckenridge Pharmaceutical, Inc

FDA Drug Moderate Jan 1, 2025

chlorproMAZINE Hydrochloride Tablets, USP, 10mg, 100-count bottle, RX only, Manufactured for: Glenmark Pharmaceuticals Inc., NJ; Product of India, ND…

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Jan 1, 2025

Kit for the Preparation of Technetium Tc 99m Sestamibi Injection, Each Kit contains: 30 sterile and non-pyrogenic reaction vials each containing Tetr…

Curium US, LLC

FDA Drug Moderate Jan 1, 2025

Duloxetine Delayed-Release Capsules, USP, 30 mg, Rx only, 90 count bottles, Manufactured by: Aurobindo Pharma Limited, Hyderabad-500 090, India, For …

Amerisource Health Services LLC

FDA Drug Moderate Jan 1, 2025

Duloxetine Delayed-Release Capsules USP, 30 mg, Rx only, 30 count bottles, Manufactured by: Aurobindo Pharma Limited, Hyderabad-500 090, India, For B…

Amerisource Health Services LLC

FDA Drug Moderate Jan 1, 2025

Duloxetine Delayed-Release Capsules, 60 mg, a) 30 count blister cards (NDC 70518-0937-04), b) 30 count bottles (NDC 70518-0937-03), Rx only, Source N…

RemedyRepack Inc.

FDA Drug Moderate Jan 1, 2025

Duloxetine Delayed-Release Capsules USP, 60 mg, Rx only, 30 count bottles, Manufactured by: Aurobindo Pharma Limited, Hyderabad-500 090, India, For B…

Amerisource Health Services LLC

FDA Drug Moderate Jan 1, 2025

chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 100-count bottle, RX only, Manufactured for: Glenmark Pharmaceuticals Inc., NJ; Product of India, N…

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Jan 1, 2025

DULoxetine DR USP, 30 mg, 90-count bottle, Rx Only, Packaged by: PD Rx Pharmaceuticals Inc, Oklahoma City, OK 73127, NDC: 43063-877-90

PD-Rx Pharmaceuticals, Inc.

FDA Drug Moderate Jan 1, 2025

UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323

MXBBB

FDA Drug Moderate Jan 1, 2025

Duloxetine Delayed-Release Capsules, USP, 60 mg, Rx Only, 90-count bottles (NDC 51991-748-90) Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, …

Breckenridge Pharmaceutical, Inc

FDA Drug Moderate Jan 1, 2025

Duloxetine Delayed-Release Capsules, USP, 60 mg, Rx only, 1,000 count bottles, Manufactured by: Aurobindo Pharma Limited, Hyderabad-500 090, India, F…

Amerisource Health Services LLC

FDA Devices Moderate Jan 1, 2025

20/30 Priority Pack Accessory Kit w/Copilot, REF: 1003327, used for cardiovascular procedures.

Abbott Vascular Inc

FDA Devices Moderate Jan 1, 2025

ST REPROCESSED BRUNS CURETTE #00 (BC00), Medline Item No. 67600K

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jan 1, 2025

Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm, Small Stature, T25, BT Model/Catalog Number: 79-0002 Software Version: N/A …

SEASPINE ORTHOPEDICS CORPORATION

FDA Devices Moderate Jan 1, 2025

KIT,SPINE LH Convenience kit, SKU DYNJ906448A.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jan 1, 2025

Magnesium Flex reagent cartridge, 360 tests, Catalog Number: K3057; Siemens Material Number (SMN): 10445158;

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jan 1, 2025

SEPTOPLASTY PACK Convenient kit, SKU DYNJ44759F. Convenience kits used for various procedures.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jan 1, 2025

Access hsTnI Reagent, REF B52699, Immunoassay Method, Troponin Subunit. For the quantitative determination of cardiac troponin I (cTnI) levels in hu…

Beckman Coulter, Inc.

FDA Devices Moderate Jan 1, 2025

20/30 Priority Pack Accessory Kit/.096 RHV, REF: 1000186, or use during vascular procedures in conjunction with interventional and / or diagnostic de…

Abbott Vascular Inc

FDA Devices Moderate Jan 1, 2025

ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500), Medline Item No. 67870

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Critical Jan 1, 2025

StatStrip Glucose Hospital Meter System. Model/Catalog Number: 63685. Prescription use blood glucose meter for near-patient testing.

Nova Biomedical Corporation

FDA Devices Moderate Jan 1, 2025

epoc NXS Host; Siemens Material Number (SMN): 11413498(JP) ; Software Version Number: 4.14.9. Intended for use by trained medical professionals as…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jan 1, 2025

STERILE MAGILL FORCEP (MAGF9), Medline Item No. 66790

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jan 1, 2025

EMPOWR 3D Knee Tibial Insert, 5R 16MM, VE, REF: 342-16-705; EMPOWR 3D Knee Tibial Insert, 3R 14MM, VE, REF: 342-14-703

Encore Medical, LP

FDA Devices Moderate Jan 1, 2025

epoc NXS Host; Siemens Material Number (SMN): 11413879(IN) ; Software Version Number: 4.14.9. Intended for use by trained medical professionals as…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Critical Jan 1, 2025

StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog Number: 63910. Prescription use blood glucose ketone meter for near-patient te…

Nova Biomedical Corporation

FDA Devices Moderate Jan 1, 2025

Panther Fusion SARS-CoV-2/Flu A/B/RSV Assay, REF: PRD-07400

Hologic, Inc.

FDA Devices Moderate Jan 1, 2025

Clarity Precision Grip Attachments, for use in orthodontic treatment. Part numbers/SKUs: 359-830 359-831 359-832 359-833 359-834 359-835 …

3M Company - Health Care Business

FDA Devices Moderate Jan 1, 2025

Medline brand, medical procedure convenience kits, labeled as: 1) CRANIOTOMY, SKU CDS982719X; 2) MVFF/FIBU #54-RF, SKU DYNJ21927Q; 3) MVFF/FIBU #54-R…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jan 1, 2025

EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706

Encore Medical, LP

FDA Devices Moderate Jan 1, 2025

Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient airways for diagnostic and therapeutic procedures.

Noah Medical

FDA Devices Moderate Jan 1, 2025

epoc NXS Host; Siemens Material Number (SMN): 11413518 (ROW) ; Software Version Number: 4.14.9. Intended for use by trained medical professionals …

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jan 1, 2025

O.R. SCISSORS, S/B, 5.5 STERILE, Medline Item No. DYND04000

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jan 1, 2025

DIEP FLAP Convenience kit, SKU DYNJ910120. Convenience kits used for various procedures.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jan 1, 2025

epoc NXS Host; Siemens Material Number (SMN): 11413475 (US); Software Version Number: 4.14.9. Intended for use by trained medical professionals as a…

Siemens Healthcare Diagnostics, Inc.

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