PlainRecalls

2026 Recalls

Compiled from official public sources by the editorial team.

2,438 recalls · Page 25 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 6 critical, 35 moderate, and 9 lower-severity recalls. The page references 19 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 (41), CPSC (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 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 Low Apr 1, 2026

Philips X3-1 Ultrasound Transducer

Philips Ultrasound, Inc

FDA Devices Low Apr 1, 2026

Philips OMNI II TEE Ultrasound Transducer

Philips Ultrasound, Inc

FDA Devices Moderate Apr 1, 2026

Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly…

Olympus Corporation of the Americas

FDA Devices Moderate Apr 1, 2026

MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 1, 2026

Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Critical Apr 1, 2026

16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile), REF: FCL-174-00/B

Merit Medical Systems, Inc.

FDA Devices Moderate Apr 1, 2026

Tandem pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to d…

Tandem Diabetes Care, Inc.

FDA Devices Moderate Apr 1, 2026

Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340.

Olympus Corporation of the Americas

FDA Devices Moderate Apr 1, 2026

I.T.S. LRS (Locking Reconstruction System) with the below descriptions and corresponding article numbers. 1. DFL (Distal Femur Locking) Distal Fe…

I.T.S. GmbH

FDA Devices Low Apr 1, 2026

Philips L17-5 Ultrasound Transducer

Philips Ultrasound, Inc

FDA Devices Critical Apr 1, 2026

BioFlo DuraMax Catheter, REF: H965103028011/A, H965103028021/A, H965103028021/EU, H965103028031/A, H965103028031/EU, H965103028041/A, H965103028041/E…

Merit Medical Systems, Inc.

FDA Devices Critical Apr 1, 2026

Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd

Navajo Manufacturing Company

FDA Devices Moderate Apr 1, 2026

Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.

Olympus Corporation of the Americas

FDA Devices Moderate Apr 1, 2026

Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;

Straumann USA LLC

FDA Devices Moderate Apr 1, 2026

I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions and corresponding article numbers. 1. Distal Tubular Plate; Articl…

I.T.S. GmbH

FDA Devices Moderate Apr 1, 2026

Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Mod…

AMO Puerto Rico Manufacturing, Inc.

FDA Devices Moderate Apr 1, 2026

Brand Name: Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3005 Product D…

Olympus Corporation of the Americas

FDA Devices Moderate Apr 1, 2026

Claviculaplate with Angular Stability, with the below descriptions and associated article numbers. 1. Anterior Clavicle Plate, Medial; Article Nu…

I.T.S. GmbH

FDA Devices Critical Apr 1, 2026

DuraMax Chronic Hemodialysis Catheter, REF: H787103028015/A, H787103028025/A, H787103028031/A, H787103028035/A, H787103028041/A, H787103028045/A, H78…

Merit Medical Systems, Inc.

FDA Devices Moderate Apr 1, 2026

Brand Name: Humeral Head Plate with Angular Stability, with the following description: Proximal Humeral Plate. Article Numbers: 211341-10, 211341-4, …

I.T.S. GmbH

FDA Devices Low Apr 1, 2026

Philips Mini Multi TEE Ultrasound Transducer

Philips Ultrasound, Inc

FDA Devices Low Apr 1, 2026

Philips OMNI III TEE Ultrasound Transducer

Philips Ultrasound, Inc

FDA Devices Moderate Apr 1, 2026

I.T.S. DUL (Distal Ulna Locking) System and UOL (Ulna Osteotomy Locking) System with the below descriptions and corresponding article numbers. 1. I.…

I.T.S. GmbH

FDA Devices Moderate Apr 1, 2026

Embrace Drill Tower, Standard/Lateral (25mm); Item Number: 645-081/63;

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Apr 1, 2026

Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;

Straumann USA LLC

FDA Devices Moderate Apr 1, 2026

FR.O.H. Calcaneus Repair System with the following description: Anterolateral Calcaneus Plate. Article Number: 21064-60.

I.T.S. GmbH

FDA Devices Low Apr 1, 2026

Philips 3D6-2 Ultrasound Transducer

Philips Ultrasound, Inc

FDA Devices Low Apr 1, 2026

Philips X7-2 Ultrasound Transducer

Philips Ultrasound, Inc

FDA Devices Moderate Apr 1, 2026

Pilonplate with Angular Stability, with the below descriptions and corresponding article numbers. 1. Anterolateral Tibia Plate; Article Numbers: …

I.T.S. GmbH

FDA Devices Moderate Apr 1, 2026

Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3006 Pro…

Olympus Corporation of the Americas

FDA Devices Moderate Apr 1, 2026

Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920005PK Product Description: The PKS Cu…

Olympus Corporation of the Americas

FDA Devices Moderate Apr 1, 2026

Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number: ES-100V3 (device); BT2M20S8C (…

Koven Technology, Inc.

FDA Devices Low Apr 1, 2026

Philips C9-4 Ultrasound Transducer

Philips Ultrasound, Inc

FDA Devices Critical Apr 1, 2026

Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use

Erbe USA Inc

FDA Devices Moderate Apr 1, 2026

Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032…

I.T.S. GmbH

FDA Devices Moderate Apr 1, 2026

MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for use in determining antimicrobial agent susceptibili…

Beckman Coulter, Inc.

FDA Devices Moderate Apr 1, 2026

Brand Name: Olympus HALO PKS Cutting Forceps, 5mm 33cm Product Name: HALO PKS Cutting Forceps Model/Catalog Number: HACF0533 Product Description: …

Olympus Corporation of the Americas

FDA Devices Low Apr 1, 2026

Philips L12-5 Ultrasound Transducer

Philips Ultrasound, Inc

FDA Devices Moderate Apr 1, 2026

Pelvic Reconstruction System (PRS) with the below descriptions and corresponding article numbers. 1. Fixation Screw; Article Number: 70312. 2…

I.T.S. GmbH

FDA Devices Moderate Apr 1, 2026

Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL PLUS, 2X2.2"

Medline Industries, LP

FDA Devices Critical Apr 1, 2026

Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.

Philips Respironics, Inc.

CPSC Moderate Mar 26, 2026

4our Kiddies Tip Restraint Kits Recalled Due to Tip-Over Hazard; Risk of Serious Injury and Death

CPSC Moderate Mar 26, 2026

AirClub Convertible Bassinets Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Bedside Sleepers

Zhangzhou Qiangxing Supply Chain Management Co., Ltd. dba AirClub of China

CPSC Moderate Mar 26, 2026

CCCEI Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Fire; Sold by Middle Way Electronics

Middle Way Electronics, of China

CPSC Moderate Mar 26, 2026

DIY Cold Plunge Recalls Sauna Heater Kits Due to Risk of Serious Injury or Death from Fire Hazard

Plunge Buddy LLC, doing business as DIY Cold Plunge, of North Mankato, Minnesota

CPSC Moderate Mar 26, 2026

DuraTrac Recalls Stainless Steel Gas Connectors Due to Fire Hazard

CPSC Moderate Mar 26, 2026

FUNTOK Ride-On Trucks Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by Shenzhen Luobei Trading

CPSC Moderate Mar 26, 2026

GLMZZ Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys

Shenzhen Jiaying E-commerce Co., Ltd., dba GLMZZ, of China

CPSC Moderate Mar 26, 2026

MPINOI Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adul…

CPSC Moderate Mar 26, 2026

Nexgrill Recalls Over 10.2 Million Metal Wire Bristle Grill Brushes Due to Ingestion Hazard; Sold at Home Depot

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.