PlainRecalls

2026 Recalls

Compiled from official public sources by the editorial team.

2,438 recalls · Page 30 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 11 critical, 37 moderate, and 2 lower-severity recalls. The page references 32 distinct recalling firms operating in 7 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (23), FDA Drug (15), NHTSA (5), 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 Mar 11, 2026

Dukal BZK Antiseptic Towelette (Benzalkonium Chloride 0.13%) 1000 Packs per case, Manufactured For: Dukal, LLC, Ronkonkoma, NY 11779, Made in USA, ND…

ACME UNITED CORPORATION

FDA Drug Moderate Mar 11, 2026

Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 84385-106-06; d) 25g, NDC 84385-1…

Harbin Jixianglong Biotech Co., Ltd.

FDA Drug Low Mar 11, 2026

Nilotinib Capsules, 200 mg per capsule, packaged in cartons, Rx only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren…

Cipla USA, Inc.

FDA Drug Critical Mar 11, 2026

MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7

StuffbyNainax

FDA Drug Moderate Mar 11, 2026

Amnesteem (Isotretinoin) Capsules, USP 40 mg, packaged in 3 x 10-Count Prescription Packs, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc., Mor…

MYLAN PHARMACEUTICALS INC

FDA Drug Moderate Mar 11, 2026

Sodium Iodide (I-131) Solution, Therapeutic Oral, packaged as a) 1 ml V-vial, NDC 69208-003-15; Order 49317, 49323, 49325, 49329, 49333, 49339, 49341…

Radnostix

FDA Drug Moderate Mar 11, 2026

Metoprolol Succinate Extended-Release Tablets, 25 mg, 100 tablets bottles (NDC: 45963-709-11) and 1,000 tablets bottles (NDC: 45963-709-96), Rx Only,…

Teva Pharmaceuticals USA, Inc

FDA Drug Moderate Mar 11, 2026

Green Guard Antiseptic Wipes (Benzalkonium Chloride 0.13%), 25 wipes per box, Distributed by Green Guard, St. Louis, MO 63045, NDC 47682-056-73

ACME UNITED CORPORATION

FDA Drug Moderate Mar 11, 2026

Metoprolol Succinate Extended-Release Tablets, 200 mg, 100 tablets bottles, Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054, NDC: 45963-678-11

Teva Pharmaceuticals USA, Inc

FDA Drug Moderate Mar 11, 2026

Cleansing Towelette (Benzalkonium Chloride 0.13%), 5"x 7", 1,000 case/Bulk, Med-Nap, Brooksville, FL 34601, Made in USA, NDC 0924-0243-00.

ACME UNITED CORPORATION

FDA Drug Moderate Mar 11, 2026

WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 5x7, 100 CT, Progressive Products, 211 S. Ridge Street, Rye Brook, NY 10573. NDC 67…

ACME UNITED CORPORATION

FDA Drug Moderate Mar 11, 2026

1) BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) 5"x7" Piedmont Sanitizing Hand Wipes, 1,000 ea Bulk, Made in USA for: Food Service Resour…

ACME UNITED CORPORATION

FDA Drug Moderate Mar 11, 2026

Metoprolol Succinate Extended-Release Tablets, Rx Only, 100 mg, 100 tablets bottles (NDC: 45963-677-11) and 1,000 tablets bottles (NDC: 45963-677-96)…

Teva Pharmaceuticals USA, Inc

FDA Drug Moderate Mar 11, 2026

Children's Healthcare of Atlanta, Instant Hand Sanitizing Wipe(Benzalkonium Chloride 0.13%), 1000 per case, Made in USA for Food Service Resources, F…

ACME UNITED CORPORATION

FDA Drug Critical Mar 11, 2026

SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China

ANTHONY TRINH, 123Herbals LLC

FDA Devices Moderate Mar 11, 2026

Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be attached to the instrument c…

Olympus Corporation of the Americas

FDA Devices Critical Mar 11, 2026

Impella RP Flex with SmartAssist. Product Code: 1000323.

Abiomed, Inc.

FDA Devices Moderate Mar 11, 2026

Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument…

Olympus Corporation of the Americas

FDA Devices Critical Mar 11, 2026

Impella RP with SmartAssist. Product Code: 0046-0035.

Abiomed, Inc.

FDA Devices Moderate Mar 11, 2026

Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Generator Model/Catalog Number: SPL-G Product Descri…

Olympus Corporation of the Americas

FDA Devices Moderate Mar 11, 2026

Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed …

B Braun Medical Inc

FDA Devices Critical Mar 11, 2026

Impella RP. Product Code: 0046-0011.

Abiomed, Inc.

FDA Devices Moderate Mar 11, 2026

EVO+ Visian Toric Implantable Collamer Lens (TICL), Model: VTICM5

Staar Surgical AG

FDA Devices Moderate Mar 11, 2026

Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description…

Aesculap Inc

FDA Devices Moderate Mar 11, 2026

Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038

ESAOTE S.P.A.

FDA Devices Moderate Mar 11, 2026

cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample supply unit, material number 08464502001 cobas pro SSU, materi…

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Mar 11, 2026

GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image Processing, Rad…

GE Healthcare

FDA Devices Moderate Mar 11, 2026

CS300 IABP. Software Version CS300 IABP C.01.

Datascope Corp.

FDA Devices Moderate Mar 11, 2026

Atellica CH Urine Albumin (UAlb). Material Number: 11537225

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Mar 11, 2026

CS100 IABP. Software Version CS100 IABP Q.01.

Datascope Corp.

FDA Devices Moderate Mar 11, 2026

Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A devi…

B Braun Medical Inc

FDA Devices Moderate Mar 11, 2026

Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A…

B Braun Medical Inc

FDA Devices Moderate Mar 11, 2026

Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System - Reusable Probes Model/Catalog Number: SPL-SR …

Olympus Corporation of the Americas

FDA Devices Moderate Mar 11, 2026

Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description: The STA¿ - …

Diagnostica Stago, Inc.

FDA Devices Moderate Mar 11, 2026

Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE, 631516PE, 636016PE, 631220PE, …

Vascutek, Ltd.

FDA Devices Moderate Mar 11, 2026

Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name: ShockPulse-SE Lithotripsy System - Reuseable Probes Model/Catalog…

Olympus Corporation of the Americas

FDA Devices Moderate Mar 11, 2026

Brand Name: HiResolution Bionic Ear System Product Name: Sky CI M90 Sound Processor Model/Catalog Number: CI-5295-150

Advanced Bionics, LLC

FDA Devices Moderate Mar 11, 2026

Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - Single Use Probes Model/Catalog Number: SPL-S …

Olympus Corporation of the Americas

NHTSA Critical Mar 11, 2026

VOLKSWAGEN 2025-2026: ELECTRICAL SYSTEM:WIRING

VOLKSWAGEN

NHTSA Critical Mar 11, 2026

VOLVO 2025: SEAT BELTS:FRONT:WARNING LIGHT/DEVICES

VOLVO

NHTSA Critical Mar 6, 2026

KIA 2026: SEAT BELTS:REAR/OTHER:ANCHORAGE

KIA

CPSC Moderate Mar 5, 2026

Cubimana Island Storm 3 In 1 Building Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for To…

Shenzhen Ruibosi Technology Co., Ltd., dba RBS Toys, of China

CPSC Moderate Mar 5, 2026

HALO Dream Recalls Magic Sleepsuits Due to Choking Hazard

CPSC Moderate Mar 5, 2026

Tomum Minoxidil Hair Serum Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-…

Belleka Inc, dba TOMUM, of China

CPSC Moderate Mar 5, 2026

Unique Brands Com Recalls Forever 21 Pajama Pants Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards …

Unique Brands Com, Inc., of New York, New York

NHTSA Critical Mar 5, 2026

CHEVROLET,GMC 2025: FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP:CONTROL/DRIVE MODULE

CHEVROLET,GMC

NHTSA Critical Mar 5, 2026

TOYOTA 2021-2024: SEATS:MID/REAR ASSEMBLY:RECLINER

TOYOTA

FDA Food Critical Mar 4, 2026

Fish Ball, Frozen, 40 pieces per pack, 200g Wt. UPC# 810093891338

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

FDA Food Moderate Mar 4, 2026

Valley Springs 100% Natural Bottled Water. Fluoride Added. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-01301 0. Bottled by Valley Springs/Artesian Gold, L…

Valley Springs Artesian Gold, LLC

FDA Food Low Mar 4, 2026

YO!MAN CUCUMBER (FRESH HUNAN FLAVOR); Ingredients: Cucumber, chili pepper, edible vegetable oil, salt, water, sugar, brewing vinegar, food additives …

TENGEN USA TRADING CORP

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.