PlainRecalls

2023 Recall Year Insight

Federal agencies issued 6,706 product recalls indexed by PlainRecalls in calendar year 2023. That represents about 6.42% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 18.4 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 135 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 2023.

On this page of 50 records, severity classification shows 13 critical, 35 moderate, and 2 lower-severity recalls. The page references 30 distinct recalling firms operating in 4 distinct product categories, with 39 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (36), NHTSA (11), FDA Drug (3), 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 2023 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 Drug Moderate Dec 20, 2023

Liothyronine Sodium Tablets, USP 5 mcg, 100-count bottle, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India. NDC 62756-589-88

SUN PHARMACEUTICAL INDUSTRIES INC

FDA Drug Low Dec 20, 2023

Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried Barbera, S.L., Barbera del Valles, Spain, Distributed by: Novartis Pharmaceuticals Corp., East Hanover, N.J. 07936, NDC 0078-1077-66

Siegfried Barbera, SL

FDA Drug Moderate Dec 20, 2023

Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 Manufactured by: Lupin Limited, Nagpur-441 108, India, NDC# 70748-153-01

Lupin Pharmaceuticals Inc.

FDA Devices Moderate Dec 20, 2023

VITROS XT 3400 Chemistry System Product Code 6844458 Running Software Version 3.8.0

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Dec 20, 2023

RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.

Encore Medical, LP

FDA Devices Moderate Dec 20, 2023

STERILE PVP SOLUTION, REF DYNDA1907

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 20, 2023

Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Iconix Knotless 1.4mm Anchor with XBraid S (Black/White) REF 3911-714-521 The Iconix Knotless anchors are intended to be used for soft-tissue to bone fixation in the foot, ankle, knee, hip, hand, wrist, elbow and shoulder.

Riverpoint Medical, LLC

FDA Devices Moderate Dec 20, 2023

Medline Leg bag, REF URO12573

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 20, 2023

STERILE POVIDONE, REF DYNDA2061

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 20, 2023

Medline Leg bag, REF DYND12574

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 20, 2023

The System is designed as a modular system with components that include an Overhead Tube Suspension with tube/collimator, wallstand, Table, X-ray generator, and cleared wireless digital detectors. The list of detectors verified and validated for use with the Discovery XR656 HD system, including their specifications, are provided in the user documentation. The System generates diagnostic The components may be combined in different configurations to meet specific customer needs. In addition, upgr

GE Hangwei Medical Systems, Co. LTD

FDA Devices Critical Dec 20, 2023

Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR) systems are Medical Electrical Systems for use as a diagnostic device.

Philips North America Llc

FDA Devices Moderate Dec 20, 2023

Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4, a component of Stratus Imaging PACS.

CHANGE HEALTHCARE CANADA COMPANY

FDA Devices Moderate Dec 20, 2023

VITROS 4600 Chemistry System Product Code 6802445 and Refurbished Product Code 6900440 Running Software Version 3.8.0

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Dec 20, 2023

STERILE BETADINE, REF DYNDA1998

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 20, 2023

Cardinal Health Clean Stool Transportation System-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: CHB900312

Meridian Bioscience Inc

FDA Devices Moderate Dec 20, 2023

TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP

Olympus Corporation of the Americas

FDA Devices Low Dec 20, 2023

Navik 3D v2, REF NAVIK3D, 3D Mapping System

APN Health LLC

FDA Devices Moderate Dec 20, 2023

Para-Pak Zn-PVA/10% Formalin-for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites Catalog Number: 301012

Meridian Bioscience Inc

FDA Devices Moderate Dec 20, 2023

Baxter Amia Automated Peritoneal Dialysis (APD) Cycler Set, REF 5C5479

Baxter Healthcare Corporation

FDA Devices Moderate Dec 20, 2023

PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610

Limacorporate S.p.A

FDA Devices Moderate Dec 20, 2023

Medline Leg bag, REF DYND12578

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 20, 2023

VITROS XT 7600 Integrated System Product Code 6844461 Running Software Version 3.8.0

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Dec 20, 2023

CARDIOHELP-i Heart Lung Support System- A blood oxygenation and carbon dioxide removal system used to pump blood through the extracorporeal bypass circuit for circulatory and/or pulmonary support for periods appropriate to cardiopulmonary bypass Part Number: 701072780, (CARDIOHELP-I US); 701048012 (CARDIOHELP-I NON US)

Maquet Medical Systems USA

FDA Devices Moderate Dec 20, 2023

STERILE PVP, REF DYNDA1649

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 20, 2023

The 4Kscore Test, an in vitro serum or plasma test that combines the results of four immunoassays (Roche Elecsys total PSA (prostate specific antigen), Roche Elecsys free PSA, intact PSA, and human kallikrein 2) into a single numerical score that also incorporates the following information: a patient s age, previous biopsy, and digital rectal exam (DRE).

BioReference Health, LLC

FDA Devices Moderate Dec 20, 2023

STERILE STERILE PREP STICK, REF DYNDA1134

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 20, 2023

The System is designed as a modular system with components that include an Overhead Tube Suspension with tube/collimator, wallstand, Table, X-ray generator, and cleared wireless digital detectors. The list of detectors verified and validated for use with the Discovery XR656 HD system, including their specifications, are provided in the user documentation. The System generates diagnostic The components may be combined in different configurations to meet specific customer needs. In addition, upgr

GE Hangwei Medical Systems, Co. LTD

FDA Devices Moderate Dec 20, 2023

Medtronic SynchroMed, Model A10

Medtronic Inc.

FDA Devices Moderate Dec 20, 2023

SagiPlan 2.2, CE0344, Rx Only , Brachyterapy Treatment Planning System

Bebig Isotopentechnik Gmbh

FDA Devices Moderate Dec 20, 2023

STERILE PVP SLN KIT, REF DYNDM1097

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Critical Dec 20, 2023

Integra LifeSciences Corp.

FDA Devices Moderate Dec 20, 2023

Sensica Urine Output System, Catalog Number SCCS1002

C.R. Bard Inc

FDA Devices Moderate Dec 20, 2023

VITROS 5600 Integrated System Product Code 6802413 and Refurbished Product Code 6802915 Running Software Version 3.8.0

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Dec 20, 2023

Para-Pak Clean Vial-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: 900312

Meridian Bioscience Inc

FDA Devices Moderate Dec 20, 2023

ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Dec 20, 2023

VITROS 3600 Immunodiagnostic System Product Code 6802783 and Refurbished Product Code 6802914 Running Software Version 3.8.0

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Dec 20, 2023

Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 OTW REF 420-006 Spectranetics Turbo-Elite Laser Atherectomy Catheter 1.4 RX REF 414-159 Spectranetics Turbo-Elite Laser Atherectomy Catheter 1.7 OTW REF 417-152 The Turbo-Elite devices are indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions in humans.

Spectranetics Corporation

FDA Devices Moderate Dec 20, 2023

PVP SOLUTION SING STRL, REF DYNDA1858

MEDLINE INDUSTRIES, LP - Northfield

NHTSA No agency class Dec 20, 2023

AUDI 2023-2024: AIR BAGS:SIDE/WINDOW

AUDI

NHTSA No agency class Dec 20, 2023

AUDI 2019-2022: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY THERMAL:MANAGEMENT:SOFTWARE

AUDI

NHTSA No agency class Dec 20, 2023

LEXUS,TOYOTA 2020-2022: AIR BAGS:SENSOR:OCCUPANT CLASSIFICATION

LEXUS,TOYOTA

NHTSA No agency class Dec 20, 2023

TOYOTA 2022-2023: AIR BAGS:FRONTAL

TOYOTA

NHTSA No agency class Dec 19, 2023

TESLA 2022-2023: LATCHES/LOCKS/LINKAGES:DOORS:LATCH

TESLA

NHTSA No agency class Dec 18, 2023

ACURA,HONDA 2013-2023: FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP

ACURA,HONDA

NHTSA No agency class Dec 15, 2023

MERCEDES-BENZ 2014-2020: STRUCTURE:BODY:ROOF AND PILLARS

MERCEDES-BENZ

NHTSA No agency class Dec 15, 2023

MERCEDES-BENZ 2022-2023: POWER TRAIN:DRIVELINE:DIFFERENTIAL UNIT

MERCEDES-BENZ

NHTSA No agency class Dec 15, 2023

MERCEDES-BENZ 2023: SUSPENSION:FRONT

MERCEDES-BENZ

NHTSA No agency class Dec 15, 2023

FORD 2022-2024: EXTERIOR LIGHTING:TURN SIGNAL:BULBS

FORD

NHTSA No agency class Dec 15, 2023

FORD 2023: STEERING:COLUMN

FORD

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2023 with 2022 →

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 2023

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 2023 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.