PlainRecalls

2025 Recalls

5,015 recalls · Page 7 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 1 critical, 49 moderate, and 0 lower-severity recalls. The page references 9 distinct recalling firms operating in 4 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (44), FDA Drug (6), 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 Drug Moderate Dec 10, 2025

Globe Clotrimazole Cream, USP, 1 %, Net Wt. 1 oz (28.4g), Distributed by: Trifecta Pharmaceuticals USA, 101 NE Third Avenue, Suite 1500, Ft. Lauderda…

Blossom Pharmaceuticals

FDA Drug Moderate Dec 10, 2025

Lanashield Skin Barrier, 4 oz. (113 g), Manfuactured for: Dynarex Corporation, 10 Gleshaw Street, Orangeburg, NY 10962 USA, Made in India, UPC 616784…

Blossom Pharmaceuticals

FDA Drug Moderate Dec 10, 2025

Nivagen, Zinc Oxide Ointment, Net Wt. 1 oz. (28.4g), Nivagen Pharmaceuticals, Inc., Sacramento, CA 95827, USA Made in India, NDC 75834-170-01.

Blossom Pharmaceuticals

FDA Drug Moderate Dec 10, 2025

Globe Clotrimazole Cream USP, 1 % Antifungal Cream, Net Wt., 5 oz. (142 g, Distributed by: Trifecta Pharmaceuticals USA, 101 NE Third Avenue, Suite 1…

Blossom Pharmaceuticals

FDA Drug Moderate Dec 10, 2025

Dynagel, Moisturizing Wound Hydrogel, Net Wt. 3oz (84.7 g), Manufactured for: Dynarex Corporation, 16 Glenshaw Street, Orangeburg, NY 10962, UPC 6178…

Blossom Pharmaceuticals

FDA Drug Moderate Dec 10, 2025

WeCare, Zinc Oxide Ointment, Net Wt. 15 oz/425 g, Manuactured for: Dynarex Corporation, 11 Dynarex Drive, Middletown, NY 10941, Made in India, NDC 67…

Blossom Pharmaceuticals

FDA Devices Moderate Dec 10, 2025

IntelliVue MP90. Product Number: M8010A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Food Intolerance Test Small

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FDA Devices Moderate Dec 10, 2025

IntelliVue MP30. Product Number: M8002A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Vitamin D-Test

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FDA Devices Moderate Dec 10, 2025

Candida Test

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FDA Devices Moderate Dec 10, 2025

Organic Acids Profile Test Large

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FDA Devices Moderate Dec 10, 2025

Allergy Test IgE

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FDA Devices Moderate Dec 10, 2025

Allergy test Small

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FDA Devices Moderate Dec 10, 2025

IntelliVue Patient Monitor MX800. Product Number: 865240.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

GI Microbiome Profile XL

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FDA Devices Moderate Dec 10, 2025

Illegally Marketed

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FDA Devices Moderate Dec 10, 2025

HPV Antigen Test

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FDA Devices Moderate Dec 10, 2025

Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,

Philips Ultrasound, LLC

FDA Devices Moderate Dec 10, 2025

Sperm Test

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FDA Devices Moderate Dec 10, 2025

Mycoplasma test, IgG and IgM

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FDA Devices Moderate Dec 10, 2025

Parasite Test

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FDA Devices Moderate Dec 10, 2025

Adrenal Test

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FDA Devices Moderate Dec 10, 2025

Neurotransmitters Plus

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FDA Devices Moderate Dec 10, 2025

Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn Two-Piece Blood Pressure Cuff.

Baxter Healthcare Corporation

FDA Devices Moderate Dec 10, 2025

Pollen Allergy Test

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FDA Devices Moderate Dec 10, 2025

Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.

Fresenius Kabi USA, LLC

FDA Devices Moderate Dec 10, 2025

Alcohol (ALC) Test Saliva

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FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test XL

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FDA Devices Moderate Dec 10, 2025

Pet Allergy Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue Patient Monitor MX700. Product Number: 865241.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

CT 5300; Software Version Number: 4.5, 5.0, 5.1;

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Urinary Tract Infection Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue Patient Monitor MX500. Product Number: 866064.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Lactose Intolerance Test

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FDA Devices Moderate Dec 10, 2025

Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S

Paragon 28, Inc.

FDA Devices Moderate Dec 10, 2025

PSA Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue Patient Monitor MX850. Product Number: 866470.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test Small

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FDA Devices Moderate Dec 10, 2025

8 in 1 STI Test Kit

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FDA Devices Moderate Dec 10, 2025

Akkermansia Test

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FDA Devices Moderate Dec 10, 2025

MAMMOMAT Inspiration;

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Dec 10, 2025

Food Intolerance Test Medium

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FDA Devices Moderate Dec 10, 2025

KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K

Microbiologics Inc

FDA Devices Moderate Dec 10, 2025

MAMMOMAT Fusion;

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Dec 10, 2025

IntelliVue MP2. Product Number: M8102A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Food Sensitivity Test Large

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FDA Devices Critical Dec 10, 2025

IVENIX INFUSION SYSTEM, LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Large Volume Infusion Pump A…

Fresenius Kabi USA, LLC

FDA Devices Moderate Dec 10, 2025

Mycotoxin Panel Test

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FDA Devices Moderate Dec 10, 2025

Food Sensitivity Test Small

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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