2025 Recalls
6,168 recalls · Page 83 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 13 critical, 37 moderate, and 0 lower-severity recalls. The page references 33 distinct recalling firms operating in 7 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (19), CPSC (10), FDA Drug (9), 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.
Intera 1.5T Power/Pulsar, Model Number: 781105;
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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.
Intera 1.5T R11, Model Number: 781170;
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2
ICU Medical, Inc.
Intera 1.5T, Model Numbers: 781195 and 781295;
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Intera 1.0T Power/Pulsar, Model Number: 781103;
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3010 Product Description: Contour Gold Eyelid Weight, 1.0 gm …
Meddev Corp
Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.
AVID Medical, Inc.
Pruitt Occlusion Catheter. Catalog Numbers: 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56
LeMaitre Vascular, Inc.
TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34, 1651-38, 1651-44, 1651-48, 1651-58, 1651-64, 1651-68, 1651-78, 1651-84, 16…
LeMaitre Vascular, Inc.
MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in corrugated shipper cases (4 bott…
Nipro Renal Soultions USA, Corporation
Intera CV, Model Number: 781107;
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation system that is …
Augmedics Ltd.
KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the…
Klinika Mdical Gmb
CMS8000 Patient Monitor
Contec Medical Systems Co., Ltd.
Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002; 2) BT-20-0002A; 3) BT-20-0002AP; 4) BT200007; 5) BT-20-0007; 6) B…
Baxter Healthcare Corporation
Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH265 Software Version: N/A Product Description: AirLi…
Vyaire Medical
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
LeMaitre Vascular, Inc.
Centurion Sterile Weitlaner Retractor, Reorder: 67315
MEDLINE INDUSTRIES, LP - Northfield
VOLKSWAGEN 2024-2025: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA
VOLKSWAGEN
RAM 2022-2025: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA
RAM
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
BuddyLove Recalls Children's Mini Danica Loungewear Sets Due to Risk of Serious Injuries or Death from Burn Hazard; Violation of Federal Regulations …
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…
Fat Brain Recalls Rollers Tile Toys Used in PlayTab Modular Activity Boards Due to Magnet Ingestion Hazard; Risk of Serious Injury or Death; Violatio…
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
KTM Recalls Off-Road Motorcycles Due to Crash Hazard Recall
KTM AG, of Austria
Leon Rading Recalls Digital Wall Clocks Due to Risk of Serious Injury or Death from Ingestion Hazard; Violations of Federal Regulations for Consumer …
LivingCaring Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violation of Federal …
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
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
TOYOTA 2022-2025: EXTERIOR LIGHTING:BACK UP LIGHTS
TOYOTA
VOLKSWAGEN 2025: SEATS:MID/REAR ASSEMBLY
VOLKSWAGEN
Trader Joe's Sesame Miso Salad with Salmon, net wt. 10.25oz., in clear plastic clamshell container, UPC 00773164
Taylor Farms Illinois Inc.
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
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
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
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
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
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
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
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.
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.
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
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 10mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, D…
FDC Limited
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
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
Carboxymethylcellulose Sodium Ophthalmic Gel 1%, Carboxymethlycellulose Sodium 1% Eye Lubricant, Lubricant Eye Gel, Soothing Gel, Sterile, 0.5 FL OZ …
BRS Analytical Services, LLC
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
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
Nearby Recall Years
Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.
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 August 2026.