PlainRecalls

2025 Recalls

6,168 recalls · Page 38 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 8 critical, 32 moderate, and 10 lower-severity recalls. The page references 21 distinct recalling firms operating in 6 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (24), FDA Drug (16), FDA Food (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.

FDA Food Critical Oct 1, 2025

Middlefield Original Cheese Co-op Shredded Mozzarella/Provolone Cheese, 5 lbs., packaged in a plastic bag, packed 4 bags per case

Middlefield Original Cheese Cooperative

FDA Food Critical Oct 1, 2025

Middlefield Original Cheese Co-op Original Swiss Cheese, packaged as 5 lb. loaves wrapped in plastic and packed 2 loaves per case (distribution) or 8…

Middlefield Original Cheese Cooperative

FDA Food Moderate Oct 1, 2025

Elderberry 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9…

Extract Labs, Inc.

FDA Food Critical Oct 1, 2025

Middlefield Original Cheese Co-op Organic Gouda Cheese, 8 oz., packaged individually in plastic, packed 12 per case

Middlefield Original Cheese Cooperative

FDA Food Critical Oct 1, 2025

1) Sunrise Creamery Dilly Pickle Monterey Jack Cheese with Dill Pickles, Net Wt. 6 oz., packaged individually in plastic, packed 12 per case, UPC: 81…

Middlefield Original Cheese Cooperative

FDA Food Critical Oct 1, 2025

1) Middlefield Original Cheese Co-op All Natural Mild Cheddar Cheese, 5 lb., packaged as individual loaves wrapped in plastic, packed 2 loaves per ca…

Middlefield Original Cheese Cooperative

FDA Food Low Oct 1, 2025

UDK ,Half Plum, 170 g, Container, 24, ambient

SUNGAL INC

FDA Food Low Oct 1, 2025

MMBAL pasteurized donor human milk (PDHM), 100 mL (3.38 fl. oz.), packaged in a BPA-free plastic bottle

Mothers' Milk Bank of Alabama

FDA Food Moderate Oct 1, 2025

Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 TH…

Extract Labs, Inc.

FDA Food Critical Oct 1, 2025

1) Middlefield Original Cheese Co-op Monterey Jack, 5 lb., packaged as loaves wrapped in plastic and packed 8 loaves per case 2) Middlefield Origina…

Middlefield Original Cheese Cooperative

FDA Drug Moderate Oct 1, 2025

Azelaic Acid Gel, 15%, 50 grams, For Topical Use Only, Rx only, Manufactured by: Glenmark Pharmaceuticals Limited Colvale-Bardez, Goa 403513, India, …

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Oct 1, 2025

edunn clarity, BP Treatment Cleanser 10% (Benzoyl Peroxide 10%), 7 oz (201g) Uptown Medi Spa, Phoenix, AZ.

Private Label Skin Care Inc.

FDA Drug Low Oct 1, 2025

TopCare Health 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The KROGER CO., Cincinnati, Ohio 45202. NDC: 36800-589-14

Consumer Product Partners, LLC

FDA Drug Low Oct 1, 2025

Kroger 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The KROGER CO., Cincinnati, Ohio 45202. NDC: 30142-810-14

Consumer Product Partners, LLC

FDA Drug Moderate Oct 1, 2025

ARTISAN OF SKIN (Benzoyl Peroxide 10%) , 7 oz (201 g), Artisan of Skin Beverly Hills, CA 90210

Private Label Skin Care Inc.

FDA Drug Low Oct 1, 2025

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed…

Granules Pharmaceuticals Inc.

FDA Drug Low Oct 1, 2025

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed…

Granules Pharmaceuticals Inc.

FDA Drug Moderate Oct 1, 2025

mel rx Skin, NO DRAMA Benzoyl Peroxide 10% Acne Treatment, 7 oz, 201 g Mel Skin Rx Beverly Hills, CA 90210

Private Label Skin Care Inc.

FDA Drug Low Oct 1, 2025

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed…

Granules Pharmaceuticals Inc.

FDA Drug Low Oct 1, 2025

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed…

Granules Pharmaceuticals Inc.

FDA Drug Moderate Oct 1, 2025

Micronized BPO Gel Cleanser 10% (Benzoyl Peroxide 10%) Pantea MD , 7 oz (201 g), University Skin Institute, 650 University Ave, Ste 200, Sacramento, …

Private Label Skin Care Inc.

FDA Drug Low Oct 1, 2025

READYPREP PVP, Povidone-Iodine 10% Solution, Topical Antiseptic, Not Sterile, 1 Gallon (3.78 L) per bottle, Manufactured in USA by Medline Industries…

Medline Industries, LP

FDA Drug Moderate Oct 1, 2025

Skin MD by Dr Monika Kiripolsky, Body Acne Cleanser (Benzoyl Peroxide 10%), 7 oz (201 g), Monika Kiripolsky, MD Beverly Hills, CA, 90211

Private Label Skin Care Inc.

FDA Drug Moderate Oct 1, 2025

Torrey Pines Dermatology & Laser Center Benzaderm BPO Cleanser 10% (Benzoyl Peroxide 10%) 7oz (201 g), Torreypines.com

Private Label Skin Care Inc.

FDA Drug Low Oct 1, 2025

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed…

Granules Pharmaceuticals Inc.

FDA Drug Moderate Oct 1, 2025

Quick Touch Alcohol Prep Pads(Isopropyl Alcohol 70%), 100 Sterile Pads per carton, AUM Pharmaceuticals, 320 Oser Ave., Hauppauge, NY 11788.

YANGZHOU YULOU PAPER PRODUCTS CO., LTD

FDA Devices Moderate Oct 1, 2025

Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m), Product Code REF 2C8519; …

Baxter Healthcare Corporation

FDA Devices Moderate Oct 1, 2025

t:slim X2 Insulin Pump with Interoperable Technology (with Tandem t:slim mobile app)

Tandem Diabetes Care, Inc.

FDA Devices Moderate Oct 1, 2025

Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K1628…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 1, 2025

Allura Xper FD20/15; Product Code: 722058; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 1, 2025

Allura Xper FD10/10 Product Codes: (1)722011, (2) 722027, (3) 722005; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Oct 1, 2025

Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION TRAY, Kit Number ACC010379…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Oct 1, 2025

Allura Xper FD20/15 OR Table; Product Code: 722059; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 1, 2025

Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting (EVH) System (VH-60…

Maquet Cardiovascular, LLC

FDA Devices Moderate Oct 1, 2025

Allura Xper FD10 OR Table Product Codes: (1)722022, (2) 722033; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Oct 1, 2025

Automated Impella Controller (AIC) with the below brands and product codes. Used with heart assist pump. 1. Impella Controller, Packaged, US; Produ…

Abiomed, Inc.

FDA Devices Moderate Oct 1, 2025

Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034

Stryker Communications

FDA Devices Moderate Oct 1, 2025

Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.

Philips North America Llc

FDA Devices Moderate Oct 1, 2025

Allura CV20; Product Code: 722031; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 1, 2025

Philips CT systems labeled as the following: 1. IQon Spectral CT, Model Number: 728332.

Philips North America Llc

FDA Devices Moderate Oct 1, 2025

Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 Model Number: 2001 UDI-DI code: 07350137521019 Inserter Adapter OTD Pinna…

ORTOMA AB

FDA Devices Moderate Oct 1, 2025

Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Oncology, Model Number: 728243. …

Philips North America Llc

FDA Devices Moderate Oct 1, 2025

Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325.

Philips North America Llc

FDA Devices Moderate Oct 1, 2025

Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 1, 2025

Allura Xper FD20 OR Table Product Codes: (1)722023, (2) 722035, (3) 722015; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 1, 2025

MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer t…

CooperVision, Inc.

FDA Devices Moderate Oct 1, 2025

Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307.

Philips North America Llc

FDA Devices Moderate Oct 1, 2025

Allura Xper FD20/20 OR Table; Product Code: 722039; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Oct 1, 2025

Philips CT systems labeled as the following: 1. Brilliance 16 Power, Model Number: 728240. 2. Brilliance CT 16 Slice, Model Number: 728246. …

Philips North America Llc

FDA Devices Moderate Oct 1, 2025

Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

Biomet, 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

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.