PlainRecalls

2025 Recalls

5,015 recalls · Page 68 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 8 critical, 42 moderate, and 0 lower-severity recalls. The page references 30 distinct recalling firms operating in 5 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (22), CPSC (10), FDA Drug (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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate May 21, 2025

Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate May 21, 2025

DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065. The Beckman Coulter DxC 500 …

Beckman Coulter Inc.

FDA Devices Moderate May 21, 2025

FoundationOne Companion Diagnostic (F1CDx)

Foundation Medicine, Inc.

FDA Devices Moderate May 21, 2025

SmartPath to dStream for 1.5T, Model Number: 782146;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate May 21, 2025

Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit

AVID Medical, Inc.

FDA Devices Moderate May 21, 2025

Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended …

Abbott Molecular, Inc.

FDA Devices Moderate May 21, 2025

Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular lesions, RPN M…

Cook Incorporated

FDA Devices Moderate May 21, 2025

Intera 1.0T Omni/Stellar, Model Number: 781102;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate May 21, 2025

Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.

AVID Medical, Inc.

FDA Devices Moderate May 21, 2025

Enterprise 1.5T, Model Number: 781145;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate May 21, 2025

PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric s…

Richard Wolf GmbH

FDA Devices Critical May 21, 2025

Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH165 Software Version: N/A Product Description: AirLi…

Vyaire Medical

FDA Devices Moderate May 21, 2025

Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time reverse transcription (RT) polymerase chain reaction…

Abbott Molecular, Inc.

FDA Devices Moderate May 21, 2025

Intera 1.5T Omni/Stellar, Model Number: 781104;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate May 21, 2025

Intera 0.5T Standard, Model Number: 781101;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate May 21, 2025

KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayT…

Klinika Mdical Gmb

FDA Devices Moderate May 21, 2025

Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3012 Product Description: Contour Gold Eyelid Weight, 1.2 gm …

Meddev Corp

FDA Devices Critical May 21, 2025

Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.

Baxter Healthcare Corporation

FDA Devices Moderate May 21, 2025

Intera 3.0T Quasar Dual, Model Number: 781150;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate May 21, 2025

Intera 1.5T Power/Pulsar, Model Number: 781105;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical May 21, 2025

iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.

Medical Depot Inc.

FDA Devices Moderate May 21, 2025

Intera 1.5T R11, Model Number: 781170;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

CPSC Moderate May 15, 2025

Boyro Baby Recalls High Chairs Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violations of Federal Regulations for High Ch…

Boyro Baby, of China

CPSC Moderate May 15, 2025

BuddyLove Recalls Children's Mini Danica Loungewear Sets Due to Risk of Serious Injuries or Death from Burn Hazard; Violation of Federal Regulations …

CPSC Moderate May 15, 2025

Child Safety Gates Recalled Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violations of Federal Regulation for Gates and E…

CPSC Moderate May 15, 2025

Fat Brain Recalls Rollers Tile Toys Used in PlayTab Modular Activity Boards Due to Magnet Ingestion Hazard; Risk of Serious Injury or Death; Violatio…

CPSC Moderate May 15, 2025

FidgetThings Recalls Chill Pill Magnetic Haptic Fidget Toys Red Bumpy Due to Risk of Serious Injury or Death from Ingestion; Violation of Federal Reg…

FidgetThings, of Las Vegas, Nevada

CPSC Moderate May 15, 2025

KTM Recalls Off-Road Motorcycles Due to Crash Hazard Recall

KTM AG, of Austria

CPSC Moderate May 15, 2025

Leon Rading Recalls Digital Wall Clocks Due to Risk of Serious Injury or Death from Ingestion Hazard; Violations of Federal Regulations for Consumer …

CPSC Moderate May 15, 2025

LivingCaring Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violation of Federal …

CPSC Moderate May 15, 2025

NICREW Submersible RGB LED Lights Recalled Due to Risk of Serious Injury or Death from Ingestion Hazard; Violations of Federal Regulations for Consum…

Nicrew Technology Co. Limited, of China

CPSC Moderate May 15, 2025

Polaris Industries Recalls Ranger XP 1000 NorthStar and Ranger XP 1000 NorthStar Crew Recreational Off-Road Vehicles Due to Injury Hazard

Polaris Industries Inc., of Medina, Minnesota

FDA Food Critical May 14, 2025

Trader Joe's Sesame Miso Salad with Salmon, net wt. 10.25oz., in clear plastic clamshell container, UPC 00773164

Taylor Farms Illinois Inc.

FDA Food Moderate May 14, 2025

Item M0053, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN* 50195500004896. Made in USA.

LAMB WESTON Inc

FDA Food Critical May 14, 2025

Heinen's Honey Roasted Peanuts, NET WT 8.25 OZ (234g), packaged in a composite can with plastic lid, 12 cans per case, Best If Used By: 10/01/2025 an…

Trophy Nut Company

FDA Food Critical May 14, 2025

Ankimo branded Monkfish Liver; NET WT. 7 OZ (200g); Imported and DIST. BY: JJWV Marketing Corporation; Santa Fe Springs, CA 90670 USA; UPC# 8 94042 0…

JJWV Marketing Corporation

FDA Food Moderate May 14, 2025

Item M7422, frozen foodservice Lamb Weston Hashbrown Patties LW Formed Oval 6/3.5LB bags per case. GTIN*10044979922687. Made in USA.

LAMB WESTON Inc

FDA Food Moderate May 14, 2025

Item M7414, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*10044979923820. Made in USA.

LAMB WESTON Inc

FDA Food Moderate May 14, 2025

Item M7204, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*10044979923813. Made in USA.

LAMB WESTON Inc

FDA Food Critical May 14, 2025

Bone & Joint Restore. 180 capsules in a plastic bottle. Shelf life two years. Store at ambient temperature. Optimal Carnivore LLC 1603 Capitol Ave St…

Optimal Carnivore, LLC

FDA Drug Moderate May 14, 2025

temper tamer, 1 US fl oz. (29.6 mL), Homeopathic Oral Spray, Manufactured by: Siddha Flower Essences, Oxnard, CA, 93030 NDC 69779-020-01.

Siddha Flower Essences, LLC.

FDA Drug Moderate May 14, 2025

Clindamycin HCl Capsule, 300 mg, QTY: 30 Capsules per bottle, Rx Only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701. NDC#: 70518-3772-02

RemedyRePack Inc.

FDA Drug Moderate May 14, 2025

Artificial Tears Ophthalmic Solution, Dextran 70.01%/Glycerin 0.2%/Hypromellose 0.3% (Eye Lubricants) Lubricant Eye Drops, STERILE, 0.5 FL OZ (15 mL)…

BRS Analytical Services, LLC

FDA Drug Moderate May 14, 2025

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 10mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, D…

FDC Limited

FDA Drug Critical May 14, 2025

Ropivacaine Hydrochloride Injection, USP, 0.5%, 500 mg per 100 mL (5mg/mL), Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Mehsana, India, , Dis…

Amneal Pharmaceuticals, LLC

FDA Drug Moderate May 14, 2025

TESTOSTERONE PELLET 100 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only,…

BSO LLC

FDA Drug Moderate May 14, 2025

Carboxymethylcellulose Sodium Ophthalmic Gel 1%, Carboxymethlycellulose Sodium 1% Eye Lubricant, Lubricant Eye Gel, Soothing Gel, Sterile, 0.5 FL OZ …

BRS Analytical Services, LLC

FDA Drug Moderate May 14, 2025

TESTOSTERONE PELLET 200 mg BLUNT, 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outs…

BSO LLC

FDA Drug Moderate May 14, 2025

FentaNYL 500mcg (2mcg/mL) and Ropivacaine HCl 250mg (0.1%) added to 250 mL, 0.9% Sodium Chloride Injection (For Epidural Use Only), Sterile, Single-U…

Apollo Care, LLC

FDA Drug Moderate May 14, 2025

Polyvinyl Alcohol Ophthalmic Solution 1.4%, Lubricant Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle, Distributed by: AvKARE, …

BRS Analytical Services, LLC

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