PlainRecalls

2026 Recalls

Compiled from official public sources by the editorial team.

2,438 recalls · Page 21 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 1 critical, 49 moderate, and 0 lower-severity recalls. The page references 17 distinct recalling firms operating in 3 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (40), 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 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 Drug Moderate Apr 8, 2026

Artificial Tears Sterile Lubricant Eye Drops (polyvinyl alcohol 0.5%, povidone 0.6%), 0.5 FL OZ (15 mL) bottles; a) LEADER, DISTRIBUTED BY CARDINAL H…

K.C. Pharmaceuticals, Inc

FDA Drug Moderate Apr 8, 2026

Ultra Lubricating Eye Drops (polyethylene 400 0.4%, propylene glycol 0.3%), Sterile, 0.5 FL OZ (15mL) bottles; a) LEADER, DISTRIBUTED BY CARDINAL HEA…

K.C. Pharmaceuticals, Inc

FDA Drug Moderate Apr 8, 2026

Sterile Eye Drops ORIGINAL FORMULA (tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15mL) bottles; a) Good Sense Sterile Eye Drops, Distributed By: Perrigo D…

K.C. Pharmaceuticals, Inc

FDA Drug Moderate Apr 8, 2026

Dry Eye Relief Eye Drops, (glycerin 0.2%, hypromellose 0.2% and polyethylene glycol 400 1%) 0.5 FL OZ (15 mL) bottles; a) GERI CARE, Distributed by: …

K.C. Pharmaceuticals, Inc

FDA Drug Moderate Apr 8, 2026

Sterile EYE DROPS REDNESS LUBRICANT (glycerin 0.25% and naphazoline HCl 0.012%), 0.5 fl oz (15 mL) bottles; a) Industrial Eye Relief, Distributed by:…

K.C. Pharmaceuticals, Inc

FDA Drug Moderate Apr 8, 2026

Bromfenac Ophthalmic Solution 0.07%, 3 ml, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, Made in Indi…

ALEMBIC PHARMACEUTICALS, INC.

FDA Drug Moderate Apr 8, 2026

Prazosin Hydrochloride Capsules, USP, 5mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ, Manufactured by: Appco Pharma…

Appco Pharma LLC

FDA Drug Moderate Apr 8, 2026

EYE DROPS Advanced Relief, (dextran 70 0.1%, polyethylene glycol 400 1% and tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15 mL) bottles, Sterile; a) Walg…

K.C. Pharmaceuticals, Inc

FDA Drug Moderate Apr 8, 2026

Sterile EYE DROPS AC (tetrahydrozoline HCl 0.05%, zinc sulfate 0.25%), 0.5 fl. oz. (15 mL) bottles; a) Best Choice, PROUDLY DISTRIBUTED BY: VALU MERC…

K.C. Pharmaceuticals, Inc

FDA Drug Moderate Apr 8, 2026

STERILE EYE DROPS SOOTHING TEARS (polyethylene glycol 400 0.4% and propylene glycol 0.3%), 0.5 OZ 0.5 fl oz (15 mL) bottles; a) Rugby LUBRICATING EY…

K.C. Pharmaceuticals, Inc

FDA Devices Moderate Apr 8, 2026

THORACIC ROBOTS, DYNJ908777B

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

SIGNA Premier systems

GE Healthcare LLC

FDA Devices Moderate Apr 8, 2026

Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 4…

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 8, 2026

MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Wrap Aprons.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra Hi…

Mentor Texas, LP.

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Leg Wraps.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 S…

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 8, 2026

Allura Xper FD20/15 OR Table; System Code: 722059;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-113TH, SCPX-123TH, SCPX-140TH, SCPX-146TH Smooth Tall Height Tissue Expan…

Mentor Texas, LP.

FDA Devices Moderate Apr 8, 2026

MiniMed 620G Insulin Pump (MMT-1750)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US.

Synthes (USA) Products LLC

FDA Devices Moderate Apr 8, 2026

BD Kiestra" ReadA; Catalog No.: 446948.

BD KIESTRA LAB AUTOMATION

FDA Devices Moderate Apr 8, 2026

Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Airway Exam Kit, DYKE1796

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Paradigm Insulin Pump (MMT-712, MMT-715)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

Azurion 5 M12; System Code: (1)722227, (2)722231;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem

Oxoid Australia Pty Limited

FDA Devices Moderate Apr 8, 2026

eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Half Aprons.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Vest

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862)

Medtronic MiniMed, Inc.

FDA Devices Critical Apr 8, 2026

Automated Impella Controller (AIC), labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, CA; Product Code:…

Abiomed, Inc.

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/Catalog Number: TFL-PLS conta…

Olympus Corporation of the Americas

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Demi Half Aprons.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD10F; System Code: 722002;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Atellica CH Enzymatic Hemoglobin A1c (A1c_E); Siemens Material Number (SMN): 11097536;

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Apr 8, 2026

CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113, 3549313, 354-9314 SILTEX Low Height Tissue Expander Style (9100, 450…

Mentor Texas, LP.

FDA Devices Moderate Apr 8, 2026

Paradigm REAL-Time Revel Insulin Pump (MMT-523, MMT-723)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCHARGE KIT

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Kilt Blockers.

Burlington Medical, 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 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.