PlainRecalls

2026 Recall Year Insight

Federal agencies issued 3,961 product recalls indexed by PlainRecalls in calendar year 2026. That represents about 3.79% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 10.9 recalls per day across the FDA, CPSC, USDA FSIS, 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 80 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 8 critical, 42 moderate, and 0 lower-severity recalls. The page references 18 distinct recalling firms operating in 5 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (35), NHTSA (7), CPSC (6), 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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Mar 4, 2026

Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1

Medtronic Perfusion Systems

FDA Devices Moderate Mar 4, 2026

Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for urologic applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528

Medline Industries, LP

FDA Devices Moderate Mar 4, 2026

Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALYSIS INSERTION, SKU CVI5200

Medline Industries, LP

FDA Devices Moderate Mar 4, 2026

Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING CHANGE SKU EBSI1498 Medline DIALYSIS DRESSING CHANGE KIT SKU EBSI1107 EBSI1596 EBSI1781 EBSI1812 Centurion DIALYSIS/PHERESUS CVC DRSG CHANGE KIT SKU DT22630 Medline DIALYSIS/PHERESIS DRESSING CHANGE KIT SKU EBSI1470 Centurion VASCATH DRESSING CHANGE TRAY SKU DT22845

Medline Industries, LP

FDA Devices Moderate Mar 4, 2026

Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/Catalog Number: 509-00-036

Encore Medical, LP

FDA Devices Moderate Mar 4, 2026

Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha

FDA Devices Moderate Mar 4, 2026

Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE, 7.1FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MJSALINE7

Medline Industries, LP

FDA Devices Moderate Mar 4, 2026

Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for urologic applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

PIE PAK Models: P2HC-A, P2HC-S, P2HC

Edermy LLC

FDA Devices Moderate Mar 4, 2026

Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Campy CVA Medium 100/PK, R01272

Remel, Inc

FDA Devices Moderate Mar 4, 2026

Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707

Encore Medical, LP

FDA Devices Moderate Mar 4, 2026

Medline Sterile Saline Wound Wash, Cleansing & Wound Irrigation, USP Normal Saline (0.9% Sodium Chloride), 7.1 FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MDSALINE7

Medline Industries, LP

FDA Devices Moderate Mar 4, 2026

Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION, Model Number: DYKM1361A; 2) TRUNK KIT 1EA, Model Number: DYKM2013; 3) TRUNK KIT 1EA, Model Number: DYKM2013A; 4) RN TRUNK KIT, Model Number: DYKM2699; 5) TRUNK KIT, Model Number: DYKTRUNK1

Medline Industries, LP

FDA Devices Moderate Mar 4, 2026

Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and treatment in urological applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU DYNDA2705 Medline CENTRAL LINE INSERTION SKU DYNJ63347A

Medline Industries, LP

FDA Devices Moderate Mar 4, 2026

Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha

FDA Devices Moderate Mar 4, 2026

Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological applications.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 4, 2026

PIE Trolley System Model: 2005

Edermy LLC

FDA Devices Moderate Mar 4, 2026

Medline Convenience Kits: 1) NAIL KIT, Model Number: POD14214

Medline Industries, LP

FDA Devices Moderate Mar 4, 2026

Adapt Pump, Model/Catalog Number: 61600200-Adapt Pump, component of Adapt support surfaces (Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, Adapt Convertible EX), sofware version 1.3.0; Mattress, Air Flotation, Alternating Pressure

Agiliti Health - Ellis

NHTSA No agency class Mar 4, 2026

AUDI 2019: LANE DEPARTURE:SOFTWARE

AUDI

NHTSA No agency class Mar 3, 2026

FORD 2021-2025: BACK OVER PREVENTION:SOFTWARE

FORD

NHTSA No agency class Mar 3, 2026

FORD,LINCOLN 2020-2024: BACK OVER PREVENTION:SOFTWARE

FORD,LINCOLN

NHTSA No agency class Mar 3, 2026

FORD,LINCOLN 2025: ENGINE AND ENGINE COOLING:EXHAUST SYSTEM:EMISSION CONTROL:GAS RECIRCULATION VALVE (EGR VALVE)

FORD,LINCOLN

NHTSA No agency class Mar 3, 2026

FORD 2025: EXTERIOR LIGHTING:HEADLIGHTS

FORD

NHTSA No agency class Mar 3, 2026

FORD 2025-2026: POWER TRAIN:AXLE ASSEMBLY:AXLE SHAFT

FORD

NHTSA No agency class Mar 3, 2026

FORD,LINCOLN 2020-2022: VISIBILITY:WINDSHIELD WIPER/WASHER:MOTOR

FORD,LINCOLN

USDA FSIS Critical Mar 3, 2026

Ajinomoto Foods North America, Inc. Expands Recall for Chicken and Pork Fried Rice, Ramen, and Shu Mai Products Due to Possible Foreign Matter Contamination

Ajinomoto Foods North America; Ajinomoto Toyo Frozen Noodle, Inc.; Ajinomoto Foods North America

USDA FSIS Moderate Mar 1, 2026

FSIS Issues Public Health Alert for Ready-To-Eat Beef Jerky Products Due to Misbranding and Undeclared Allergen

Punahele Jerky Company, Inc.

CPSC No agency class Feb 26, 2026

Andersen Windows Recalls Window Opening Control Devices Sold as Kits or Installed on 100 Series Casement Windows Due to Fall and Serious Injury Hazards

Andersen Windows, Inc., of Bayport, Minnesota

CPSC No agency class Feb 26, 2026

Babysense Max View Baby Monitors Recalled Due to Fire Hazard; Manufactured by Hisense

Hisense Ltd., of Israel

CPSC No agency class Feb 26, 2026

Bicystar High Chairs Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violates Mandatory Standard for High Chairs

Hebei Beihong Kejiyouxiangongsi, dba Bicystar Group Co., Ltd. and Bicystar Store, of China

CPSC No agency class Feb 26, 2026

Dupray USA Recalls Neat Steam Cleaners Due to Risk of Burn Hazards or Serious Injury

CPSC No agency class Feb 26, 2026

Evajoy Above-Ground Pools 48 Inches and Taller Recalled Due to Drowning Hazard; Manufactured by Shenzhen Danya Tech

Shenzhen Danya Tech Co., Ltd. d/b/a Evajoy, of China

CPSC No agency class Feb 26, 2026

Grtard Magnetic Stick Figure Toy Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys

Shanghaijinlianwangluokejiyouxiangongsi (Shanghai Jinlian Network Technology Co., Ltd.), dba Grtard, of China

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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2026

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2026 across the FDA, CPSC, USDA FSIS 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 September 2026.