PlainRecalls

2026 Recalls

2,438 recalls · Page 42 of 49

2026 Recall Year Insight

Federal agencies issued 2,438 product recalls indexed by PlainRecalls in calendar year 2026. That represents about 2.40% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 6.7 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 49 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 2026.

On this page of 50 records, severity classification shows 7 critical, 43 moderate, and 0 lower-severity recalls. The page references 22 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 (36), CPSC (10), NHTSA (4), 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 2026 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 Feb 4, 2026

Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. MR systems with SW version R11.1 and R12.1.

Philips North America

FDA Devices Moderate Feb 4, 2026

PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010

Cerapedics, Inc.

FDA Devices Moderate Feb 4, 2026

Toothbrushes, labeled as: ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT; COLGATE TOOTH BRUSH MED. 12CT; ADULT TOOTHPASTE W BRUSH (WHITENING) 6.4oz/24ct; …

GOLD STAR DISTRIBUTION INC

FDA Devices Moderate Feb 4, 2026

Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with SW version R11.1 and R12.1.

Philips North America

FDA Devices Moderate Feb 4, 2026

Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK, Kit SKU DYNJ35494C; 2) SMJ C-SECTION PACK-LF, Kit SKU DYNJ38582O; 3)…

Medline Industries, LP

FDA Devices Moderate Feb 4, 2026

Alphenix INFX-8000F, interventional fluoroscopic x-ray system

Canon Medical System, USA, INC.

FDA Devices Moderate Feb 4, 2026

Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100 Software Version: Software…

Zimmer Surgical Inc

FDA Devices Moderate Feb 4, 2026

SmartPath to dStream for XR and 3.0T. Product Code (REF): 781270. MR systems with SW version R11.1 and R12.1.

Philips North America

FDA Devices Moderate Feb 4, 2026

Ingenia Ambition X. Product Code (REF): (1) 781356, (2) 782109, (3)782138. MR systems with SW version R11.1 and R12.1.

Philips North America

FDA Devices Moderate Feb 4, 2026

Medline medical procedure convenience kits labeled as: 1) CATH LAB PACEMAKER PACK-LF, Kit SKU DYNJ64837C; 2) LOOP RECOVERY PACK, Kit SKU DYNJT70…

Medline Industries, LP

FDA Devices Moderate Feb 4, 2026

Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF, Kit SKU DYNJ20028L; 2) NEURO MINOR PACK, Kit SKU DYNJ46546M; …

Medline Industries, LP

FDA Devices Moderate Feb 4, 2026

Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137. MR systems with SW version R11.1 and R12.1.

Philips North America

FDA Devices Moderate Feb 4, 2026

Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY PACK-LF, Kit SKU DYNJ0395022O; 2) PELVISCOPY PACK-LF, Kit SKU DYNJ0…

Medline Industries, LP

FDA Devices Moderate Feb 4, 2026

Upgrade to MR 7700. Product Code (REF): 782130. MR systems with SW version R11.1 and R12.1.

Philips North America

FDA Devices Moderate Feb 4, 2026

AlternatiV+ Max Knotless Anchor

Aju Pharm Co., Ltd.

FDA Devices Critical Feb 4, 2026

Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer Model/Catalog Number: 7730ALS Software Version: Not Applicable Produc…

SunMed Holdings, LLC

FDA Devices Moderate Feb 4, 2026

Genesis Dual Thread Screw-In Anchor

Aju Pharm Co., Ltd.

FDA Devices Moderate Feb 4, 2026

Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TRO…

GOLD STAR DISTRIBUTION INC

FDA Devices Moderate Feb 4, 2026

Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23

LimFlow, Inc.

FDA Devices Critical Feb 4, 2026

Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Version: Not Applicable Product De…

SunMed Holdings, LLC

FDA Devices Moderate Feb 4, 2026

Alphenix INFX-8000H, interventional fluoroscopic x-ray system

Canon Medical System, USA, INC.

FDA Devices Moderate Feb 4, 2026

Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T; Siemens Material Number (SMN): 11574003; With Software Version VB10D-SP02

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 4, 2026

PREGNANCY TEST 24CT

GOLD STAR DISTRIBUTION INC

FDA Devices Moderate Feb 4, 2026

Alphenix INFX-8000V, interventional fluoroscopic x-ray system

Canon Medical System, USA, INC.

FDA Devices Moderate Feb 4, 2026

Genesis Screw-In Anchor

Aju Pharm Co., Ltd.

FDA Devices Moderate Feb 4, 2026

Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF, Kit SKU DYNJ0972604A; 2) PACEMAKER/ICD PACK, Kit SKU DYNJ338…

Medline Industries, LP

FDA Devices Moderate Feb 4, 2026

Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW version R11.1 and R12.1.

Philips North America

FDA Devices Critical Feb 4, 2026

Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Produ…

SunMed Holdings, LLC

FDA Devices Moderate Feb 4, 2026

Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, Kit SKU DYNJ0660040R; 2) PLASTICS VCH, Kit SKU DYNJ39225K; …

Medline Industries, LP

FDA Devices Moderate Feb 4, 2026

Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT

GOLD STAR DISTRIBUTION INC

FDA Devices Moderate Feb 4, 2026

Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS, Kit SKU CDS984347O; 2) HEAD AND NECK CDS-LF, Kit SKU CDS984857N; 3) …

Medline Industries, LP

FDA Devices Moderate Feb 4, 2026

Alphenix INFX-8000C, interventional fluoroscopic x-ray system

Canon Medical System, USA, INC.

FDA Devices Moderate Feb 4, 2026

Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conductivity Standard Solutions are a…

NIPRO Technical Services, Inc.

FDA Devices Moderate Feb 4, 2026

Brand Name: Elekta Medical Linear Accelerator Product Name: Elekta Synergy, Elekta Harmony, Elekta Infinity, Versa HD Software Version: N/A Produc…

Elekta, Inc.

FDA Devices Moderate Feb 4, 2026

Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK, Kit SKU DYNJ16826O

Medline Industries, LP

FDA Devices Moderate Feb 4, 2026

BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System with Guardrails" Suite MX is a modular infusion pump and mon…

CareFusion 303, Inc.

CPSC Moderate Feb 4, 2026

Scepter Fuel Containers Recalled Due to Risk of Serious Injury or Death from Flash Fire, Burn and Child Poisoning; Violates Mandatory Standards for P…

NHTSA Critical Feb 4, 2026

FREIGHTLINER 2025: STEERING:GEAR BOX (OTHER THAN RACK AND PINION)

FREIGHTLINER

NHTSA Critical Feb 3, 2026

FORD 2023-2024: STRUCTURE:FRAME AND MEMBERS

FORD

NHTSA Critical Feb 2, 2026

JEEP,RAM 2024-2026: EXTERIOR LIGHTING:BRAKE LIGHTS

JEEP,RAM

NHTSA Critical Jan 30, 2026

BMW,TOYOTA 2021-2024: ELECTRICAL SYSTEM:STARTER ASSEMBLY

BMW,TOYOTA

CPSC Moderate Jan 29, 2026

AiTuiTui Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon …

Shenzhen Mailesi Technology Co., Ltd., dba Vanfun, of China

CPSC Moderate Jan 29, 2026

Bazic Products Recalls Bazic Silicone Glue Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resista…

CPSC Moderate Jan 29, 2026

Gazelle USA Recalls Urban Arrow FamilyNext Pro Cargo E-Bikes Due to Injury Hazard

CPSC Moderate Jan 29, 2026

Hobby Lobby Recalls Giraffe and Llama Plush Toys with Clips Due to Choking Hazard

CPSC Moderate Jan 29, 2026

Hobby Lobby Recalls Giraffe and Llama Plush Toys with Clips Due to Drowning Hazard; Manufactured by Starmatrix Group Drowning Hazard; Manufactured by…

Starmatrix Group Inc., of China

CPSC Moderate Jan 29, 2026

LuxJet Submersible LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Produc…

Shenzhen Shimei Lighting Co., Ltd dba as Luxjet, of China

CPSC Moderate Jan 29, 2026

Mindbodygreen Recalls Ultimate Multivitamin+ Dietary Supplement Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandato…

Arizona Nutritional Supplements, of Chandler, Arizona

CPSC Moderate Jan 29, 2026

Northern Tool + Equipment Recalls Hot Water Pressure Washers Due to Fire Hazard

Northern Tool + Equipment Manufacturing, of Faribault, Minnesota

CPSC Moderate Jan 29, 2026

Primark Recalls The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets Due to Ingestion Hazard

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 2026

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 2026 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.