PlainRecalls

2020 Recalls

5,939 recalls · Page 119 of 119

2020 Recall Year Insight

Federal agencies issued 5,939 product recalls indexed by PlainRecalls in calendar year 2020. That represents about 7.07% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 16.3 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 119 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 39 records, severity classification shows 6 critical, 27 moderate, and 6 lower-severity recalls. The page references 22 distinct recalling firms operating in 3 distinct product categories, with 39 of 39 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (31), FDA Food (4), FDA Drug (4), 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 Food Moderate Jan 1, 2020

White Castle Sliders - Cheese Sliders - Cheeseburgers UPC 8298801006 (6pk Cheeseburger), UPC 829880116 (16pk Cheeseburger)

White Castle Intl

FDA Food Critical Jan 1, 2020

Okami OK Tempura Shrimp Roll, 6pc w/ Sweet and Dynamite Sauce, SKU 28114

Fuji Food Products, Inc.

FDA Food Moderate Jan 1, 2020

R.H. Macys & Co. Roasted Salted Cherries Berries and Nuts with Dark Chocolate, in 10oz metal tin, UPC - 788709600362

Ferris Coffee and Nut Company, Inc.

FDA Food Critical Jan 1, 2020

Okami brand 8pc Brown Rice Classic California Roll, SKU 28122

Fuji Food Products, Inc.

FDA Drug Low Jan 1, 2020

NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex Bag, High Alert, Rx Only, Pha…

Pharmedium Services, LLC

FDA Drug Low Jan 1, 2020

NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Injection USP (32 mcg per mL) Total Volume 258.00 mL Viaflex Bag, High Alert, Rx Only, Pha…

Pharmedium Services, LLC

FDA Drug Moderate Jan 1, 2020

Estriol [(16a, 17B)-Estra-1,3,5(10)-triene-3,16,17-triol; Oestriol] Micronized, USP, CAS 50-27-1, packaged in a) 1 G glass bottles, b) 5 G glass bott…

Spectrum Laboratory Products

FDA Drug Low Jan 1, 2020

NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 254.00 mL Viaflex Bag, High Alert, Rx Only, Pha…

Pharmedium Services, LLC

FDA Devices Moderate Jan 1, 2020

BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The core needle biopsy device is intended for use in obtaining biopsies from soft ti…

Bard Peripheral Vascular Inc

FDA Devices Moderate Jan 1, 2020

ElectroTek Temporal Sensor Cable Gold - Long Length, Graduated - Product Usage: The electroencephalographic system ElectroTek is intended to acquire,…

LIFELINES NEURO COMPANY

FDA Devices Moderate Jan 1, 2020

PTS Panels CHOL+HDL+GLU Test Strips, Reference Number 5412, for use on CardioChek PA or CardioChek Plus analyzers

Polymer Technology Systems, Inc.

FDA Devices Critical Jan 1, 2020

VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy

LivaNova USA Inc

FDA Devices Moderate Jan 1, 2020

Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent System devices are designed to deliver a flexible, self-expanding endolumin…

Cardinal Health Inc.

FDA Devices Moderate Jan 1, 2020

ApexPro Telemetry System - Product Usage: The ApexPro Telemetry System is intended for use under the direct supervision of a licensed healthcare prac…

GE Healthcare, LLC

FDA Devices Moderate Jan 1, 2020

Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHRWR1000 - Product Usage: The device can assist in the diagnosis and treatme…

Axis-Shield Diagnostics, Ltd.

FDA Devices Moderate Jan 1, 2020

CIC Pro Clinical Information Center Central Station - Product Usage: The intended use is to provide clinicians with adult, pediatric and neonatal pat…

GE Healthcare, LLC

FDA Devices Critical Jan 1, 2020

Babi.Plus Bubble PAP Valve with 12.5 cm H2O Pressure Relief Manifold, REF 1002, Rx Only, UDI: 24710810093559

Galemed Corporation

FDA Devices Moderate Jan 1, 2020

Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868

Mazor Robotics Ltd

FDA Devices Moderate Jan 1, 2020

RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0 - Product Us…

RAYSEARCH LABORATORIES AB

FDA Devices Moderate Jan 1, 2020

Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHRWR100 - Product Usage: The device can assist in the diagnosis and treatmen…

Axis-Shield Diagnostics, Ltd.

FDA Devices Moderate Jan 1, 2020

Lamicel 10PK 10MM INTL

Medtronic Xomed, Inc.

FDA Devices Moderate Jan 1, 2020

STA SYSTEM CONROL N + P (ref. 00678)

Diagnostica Stago, Inc.

FDA Devices Moderate Jan 1, 2020

CARESCAPE Central Station - Product Usage: The intended use is to provide clinicians with adult, pediatric and neonatal patient data within a hospita…

GE Healthcare, LLC

FDA Devices Moderate Jan 1, 2020

ElectroTek Temporal Sensor Cable Gold - Long Length, Single Length - Product Usage: The electroencephalographic system ElectroTek is intended to acqu…

LIFELINES NEURO COMPANY

FDA Devices Moderate Jan 1, 2020

CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable Radiofrequency Cannulae are provid…

Abbott Medical

FDA Devices Critical Jan 1, 2020

Babi.Plus 12.5 cm H2O Pressure Relief Manifold, REF 1030, RX Only, UDI: 04710810093562

Galemed Corporation

FDA Devices Low Jan 1, 2020

AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment of calibrators/controls. Part Number: 020706

Tosoh Smd Inc

FDA Devices Critical Jan 1, 2020

Babi.Plus 12.5 cm H2O Pressure Relief Manifold with Gas Supply Tube and Oxygen Sensor Port, REF 2691, Rx Only, UDI: 04710810100802

Galemed Corporation

FDA Devices Moderate Jan 1, 2020

Lamicel 20PK 5MM INTL

Medtronic Xomed, Inc.

FDA Devices Moderate Jan 1, 2020

3M Durapore Advanced, Surgical Tape, Model Numbers: 1590-0, 1590-1, 1590-2, 1590-3, 1591-0, 1591-1, 1591-2, 1591-3, 1590S-1, 1590S-2, 1590B-118, 1590…

3M Company - Health Care Business

FDA Devices Moderate Jan 1, 2020

STA UNICALIBRATOR (ref. 00675)

Diagnostica Stago, Inc.

FDA Devices Moderate Jan 1, 2020

Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHBC100 - Product Usage: The device can assist in the diagnosis and treatment…

Axis-Shield Diagnostics, Ltd.

FDA Devices Moderate Jan 1, 2020

S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent System. The SMART stent system includes a self-expanding stent made of N…

Cardinal Health Inc.

FDA Devices Low Jan 1, 2020

INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453

AAP Implantate Ag

FDA Devices Moderate Jan 1, 2020

Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T. CONTROL and S.M.A.R.T. Vascular Stent Systems consist of a self-expan…

Cardinal Health Inc.

FDA Devices Low Jan 1, 2020

INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425

AAP Implantate Ag

FDA Devices Moderate Jan 1, 2020

Urine Electrolyte Diluent, Product Code: 1112352 - Product Usage: used to dilute urine specimens for analysis of sodium (Na+) and potassium (K+) on V…

Ortho Clinical Diagnostics Inc

FDA Devices Moderate Jan 1, 2020

Lamicel 20PK 3MM INTL Cervical dilator

Medtronic Xomed, Inc.

FDA Devices Moderate Jan 1, 2020

7% BSA (Bovine Serum Albumin), Product Code: 8262487 - Product Usage: is used to dilute samples when assay values exceed the reportable (dynamic) ran…

Ortho Clinical Diagnostics 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