PlainRecalls

2020 Recalls

5,998 recalls · Page 74 of 120

2020 Recall Year Insight

Federal agencies issued 5,998 product recalls indexed by PlainRecalls in calendar year 2020. That represents about 5.90% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 16.4 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 120 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 2020.

On this page of 50 records, severity classification shows 5 critical, 44 moderate, and 1 lower-severity recalls. The page references 33 distinct recalling firms operating in 7 distinct product categories, with 48 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (34), CPSC (6), FDA Drug (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 2020 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 Moderate May 6, 2020

Velofix SA cervical cage, REF: TSA161207, TSA161208, TSA161209, TSA161210, TSA161407, TSA161408, TSA161409, TSA161410 - Product Usage:The device is i…

U&I CORP.

FDA Devices Moderate May 6, 2020

Leksell Vantage Stereotactic System. Instrument Carrier, Part of Leksell Vantage Arc (1053958). Neurological stereotaxic Instrument

Elekta Inc

FDA Devices Moderate May 6, 2020

iLab Polaris Multi-Modality Guidance System; iLab Ultrasound Imaging System

Boston Scientific Corporation

FDA Devices Moderate May 6, 2020

Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number: 60-7070-105, UDI: 00885825013868, Reprocessed Tourniquet Cuff - Produc…

Stryker Sustainability Solutions

FDA Devices Moderate May 6, 2020

Atellica CH 930 Analyzer, Siemens Material Number 11067000 with software version v1.21.0 SP1 or lower

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate May 6, 2020

CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)10885403108402(17) …

Becton Dickinson & Company

FDA Devices Moderate May 6, 2020

T12. Incorporates wireless electrocardiographic technology to achieve the real-time acquisition and RF transmission of simultaneous 12-lead ECG data …

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Trial Kit, Ref # 36990 - Product Usage: The intended use of this device is…

Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

FDA Devices Moderate May 6, 2020

Obalon Balloon System with Model 4300 Touch Dispenser Touchscreen; Software version 02.00.00.0076 - Product Usage: The System is intended to be used …

Obalon Therapeutics Inc

FDA Devices Critical May 6, 2020

Langston Dual Lumen Catheter 6F Model 5540. For delivery of contrast medium in angiographic studies

Vascular Solutions, Inc.

FDA Devices Moderate May 6, 2020

CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit

Avanos Medical, Inc.

FDA Devices Moderate May 6, 2020

Q-Tel. The Q-Tel RMS system is a computer-based cardiac and pulmonary rehabilitation data acquisition and editing system.

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.

Philips North America, LLC

FDA Devices Moderate May 6, 2020

SYNCHRON Systems Barbiturates Reagent (BARB 1 X 250); Catalog No. 475012 - Product Usage: BARB reagent, in conjunction with UniCel DxC 600/800 System…

Beckman Coulter Inc.

FDA Devices Moderate May 6, 2020

Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer

GE Healthcare, LLC

FDA Devices Low May 6, 2020

VITROS Immunodiagnostic Products TT4 Reagent Pack, Product Code 8744468

Ortho Clinical Diagnostics

FDA Devices Moderate May 6, 2020

Elekta MONACO RTP Sytem, radiation treatment planning software system - Product Usage: The Monaco system is used to make treatment plans for patients…

Elekta Inc

FDA Devices Moderate May 6, 2020

Prismaflex System, Prismaflex Control Unit

Baxter Healthcare Corporation

FDA Devices Moderate May 6, 2020

Prismaflex System, Prismaflex Control Unit

Baxter Healthcare Corporation

FDA Devices Moderate May 6, 2020

Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of real time ECG display, heart rate measurement, ST analysis and ventricular ec…

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

Phillips Azurion 7 M20, Angiographic X-Ray System Code 722079 Image guidance in diagnostic, interventional and minimally invasive surgery procedur…

Philips North America, LLC

FDA Devices Moderate May 6, 2020

ELI PC. The ELI PC Service automatically converts resting ECG recordings collected with WAM PC patient cables and WebUpload into DICOM 12-lead ECG Wa…

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

Prismaflex System, Prismaflex Control Unit

Baxter Healthcare Corporation

FDA Devices Moderate May 6, 2020

Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer

GE Healthcare, LLC

FDA Devices Moderate May 6, 2020

Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test; Material Number 425-2260; Lot number 18200A - Product Usage: The assay is an aid in the d…

Bio-Rad Labs

FDA Devices Moderate May 6, 2020

Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is A…

Allied Vision Group Inc

FDA Devices Moderate May 6, 2020

S4 and patient cable for the S4 Wireless Telemeter with the following device names: CABLE 10 WIRE LF ECG SNAP ENDS AHA GRAY, CABLE 10 WIRE LF ECG SNA…

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product Usage: Portex lumbar puncture trays provide all the materials necessary t…

Smiths Medical ASD Inc.

FDA Devices Moderate May 6, 2020

ICU Medical Cogent Hemodynamic Monitoring System, Cogent Item Number 58400-000, UDI: (01)00840619079499

ICU Medical, Inc.

FDA Devices Moderate May 6, 2020

H12+ and patient cable for the H12+ Holter Recorders with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP, PAT CBL 10WIRE LEADFORM IEC SN…

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

ABL800 FLEX model number 393-800 and 393-801, UDI:(01)05700693938004

Radiometer Medical ApS

FDA Devices Moderate May 6, 2020

CapsoCAM Plus, UDI: 00867770000209

Capso Vision, Inc.

FDA Devices Moderate May 6, 2020

Prismaflex System, Prismaflex Control Unit

Baxter Healthcare Corporation

CPSC Moderate May 6, 2020

Prepac Recalls 4-Drawer Chests Due to Tip-Over and Entrapment Hazards. In-Home Remedy May Be Delayed Due to COVID-19 Restrictions; Keep Product Away …

Prepac Manufacturing Ltd., of Canada

NHTSA Critical May 5, 2020

FORD,RAM 2019-2020: SEAT BELTS:FRONT:RETRACTOR

FORD,RAM

NHTSA Critical May 4, 2020

HYUNDAI 2016: AIR BAGS:FRONTAL

HYUNDAI

CPSC Moderate May 1, 2020

Epson Recalls Power Adapters Sold with Epson Scanners Due to Burn and Fire Hazards

CPSC Moderate Apr 30, 2020

Bellman & Symfon Recalls Flash Receivers for Reduced Hearing Persons; Unit Can Fail to Alert in an Emergency

Bellman & Symfon AB, of Sweden

CPSC Moderate Apr 30, 2020

Essential Trading Post Recalls Wintergreen and Birch Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (…

Essential Trading Post, of New Bedford, Mass.

CPSC Moderate Apr 30, 2020

Modular Robotics Recalls Rechargeable Battery Packs Due to Burn Hazard

CPSC Moderate Apr 30, 2020

Ximi Vogue Recalls Children's Neck Pillows Due to Violation of the Federal Lead Paint Ban; Risk of Poisoning

FDA Food Critical Apr 29, 2020

Lake Champlain CHOCOLATES, COIN DARK BULK ORG, NET WT 48 OZ (1.3 kg), APPROX 186 PIECES, INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA …

Champlain Chocolate Company

FDA Food Critical Apr 29, 2020

Enoki Mushroom; 7.5oz (200g); UPC #831211204181; packed in clear plastic bag with green label; imported from Green Co. located in Korea; distributed …

H & C Food Inc.

FDA Drug Moderate Apr 29, 2020

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr), 30-count box, Rx only, Manufactured for Noven Therapeutics, LL…

Noven Therapeutics, LLC

FDA Drug Moderate Apr 29, 2020

PEPPERMINT LIP MOISTURIZER (oxybenzone (4%) and Octinoxate (7%) SPF 15, 4.2 g tube, labeled as a) Bimark Inc., bimark.com; b) NOCO TRAIL REPORT, www.…

Yusef Manufacturing Laboratories, LLC

FDA Drug Moderate Apr 29, 2020

Cefixime for Oral Suspension USP, 100mg/5mL, Rx Only, Manufactured for: Lupin Pharmaceutical, Inc. Baltimore, Maryland 21202 United States, Manufactu…

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Apr 29, 2020

Lisinopril Tablets USP, 20 mg, 1000-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore MD 21202, Manufactured by: Lupin L…

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Apr 29, 2020

Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours (2.2 mg/hr) 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC…

Noven Therapeutics, LLC

FDA Drug Moderate Apr 29, 2020

Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours (3.3 mg/hr) 30-count box, Rx only, Manufactured for Noven Therapeutics, LLC…

Noven Therapeutics, LLC

FDA Devices Moderate Apr 29, 2020

Medivators Endo Smartcap Endoscope Tubing. REF100145CO2EXTU, packaged as Contents 1, 10, 50. Tubing for Olympus 140/240, 160/260, 180/280, 190/29…

Medivators, Inc.

Nearby Recall Years

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

Compare 2020 with 2019 →

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 2020

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 2020 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 August 2026.