PlainRecalls

2026 Recalls

Compiled from official public sources by the editorial team.

2,438 recalls · Page 22 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, 44 moderate, and 0 lower-severity recalls. The page references 16 distinct recalling firms operating in 1 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 Critical Apr 8, 2026

Purge Cassette, sold within Impella Pump Sets and Individually Packaged. Labeled and distributed in the below configurations and corresponding produc…

Abiomed, Inc.

FDA Devices Moderate Apr 8, 2026

Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J 3.…

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-157LH Smooth Low Height Tissue Expander, 650cc

Mentor Texas, LP.

FDA Devices Moderate Apr 8, 2026

Allura Xper FD20/10; System Code: 722029;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tiss…

Mentor Texas, LP.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Protective Sleeves.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 S…

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 8, 2026

ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description:…

ReCor Medical Inc.

FDA Devices Moderate Apr 8, 2026

Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT, DYKE2091 2. BRONCHSCOPY, DYNJ900898G DYNJ901922I 3. BRONCHSCOPY PA…

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.

Ultradent Products, Inc.

FDA Devices Moderate Apr 8, 2026

MiniMed 530G Insulin Pump (MMT-551, MMT-751)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Frontal Aprons

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00

Reflexion Medical, Inc.

FDA Devices Moderate Apr 8, 2026

MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth…

Mentor Texas, LP.

FDA Devices Critical Apr 8, 2026

Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.

Philips Respironics, Inc.

FDA Devices Critical Apr 8, 2026

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

Philips Respironics, Inc.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Blockers.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Exp…

Mentor Texas, LP.

FDA Devices Moderate Apr 8, 2026

Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved Scissors Instrument Model/Catalog …

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 8, 2026

eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Apr 8, 2026

Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.

Baxter Healthcare Corporation

FDA Devices Critical Apr 8, 2026

Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.

Philips Respironics, Inc.

FDA Devices Moderate Apr 8, 2026

Allura Xper FD20/20 OR Table; System Code: 722039;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK, DYKE2096 2. NON MB BRONCHOPSCOPY CCH LH PK, DYNJT6182 3. PULMONARY BR…

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TF…

Olympus Corporation of the Americas

FDA Devices Moderate Apr 8, 2026

Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter Model/Catalog Number: FS252251502 Product Description: 5 F…

SUMMA THERAPEUTICS, LLC

FDA Devices Moderate Apr 8, 2026

Sterile Radiology Procedure Kits, Model Number DYNDH1491B

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog N…

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 8, 2026

MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Thyroid Shield.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

Stryker Communications

FDA Devices Moderate Apr 8, 2026

Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Caps.

Burlington Medical, LLC

FDA Devices Critical Apr 8, 2026

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

Philips Respironics, Inc.

FDA Devices Moderate Apr 8, 2026

Allura Xper FD20/15; System Code: 722058;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Allura Xper FD20/20; System Code: 722038;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Kilt

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Sof…

Intuitive Surgical, Inc.

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.