PlainRecalls

2020 Recall Year Insight

Federal agencies issued 6,048 product recalls indexed by PlainRecalls in calendar year 2020. That represents about 5.79% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 16.6 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 121 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 17 critical, 32 moderate, and 1 lower-severity recalls. The page references 33 distinct recalling firms operating in 8 distinct product categories, with 37 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (15), NHTSA (13), FDA Food (12), 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, 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 Dec 16, 2020

VNS Therapy SENTIVA DUO # 1000-D - Product Usage: indicated for the treatment of chronic or recurrent depression in patients who are experiencing a treatment-resistant or treatment- intolerant depressive episode.

LivaNova USA Inc

FDA Devices Moderate Dec 16, 2020

Bransist Safire, Digital Angiography System containing a MS-200 Ceiling Suspended C-arm Support - Product Usage: designed to provide fluoroscopic images of the patient during diagnostic surgical and interventional angiography and cardiology procedures.

Shimadzu Medical Systems

FDA Devices Moderate Dec 16, 2020

Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport inside and outside of the hospital environment.

Philips North America Llc

FDA Devices Moderate Dec 16, 2020

Randox Mg R1 - Product Usage: For the quantitative in vitro determination of Magnesium in serum, plasma and urine Catalogue Number: MG3880

Randox Laboratories Ltd.

FDA Devices Moderate Dec 16, 2020

BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for immunophenotyping by flow cytometry.

Becton, Dickinson and Company, BD Biosciences

FDA Devices Moderate Dec 16, 2020

Trinias, Digital Angiography System containing a MH-200, Ceiling Suspended C-arm Support - Product Usage: intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic procedures.

Shimadzu Medical Systems

FDA Devices Moderate Dec 16, 2020

Clinical Innovations ROM Plus Collection Kit IFU: ROM Plus Rupture of Membrane Test ROM-5025, ROM-6025

Clinical Innovations, LLC

FDA Devices Moderate Dec 16, 2020

MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery Ref: MTC 23S

Mani, Inc. - Kiyohara Facility

FDA Devices Moderate Dec 16, 2020

MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S

Mani, Inc. - Kiyohara Facility

FDA Devices Moderate Dec 16, 2020

Canon Aquilion Prime SP, Multislice Helical CT Scanner, TSX-303B/8L - Product Usage: intended to acquire and display cross-sectional volumes of the whole body, including the head.

Canon Medical System, USA, INC.

FDA Devices Moderate Dec 16, 2020

Evolut (TM) R System. With the following model numbers: a. EVOLUTR-23, Labeled as VLV EVOLUTR-23 VT IR 6L COMM OUS, VLV EVOLUTR-23 TAV EVOLUT R CE 29L MX, VLV EVOLUTR-23 TAV CE AU 2Y MX, VLV EVOLUTR-23 TAV JPN MX, VLV EVOLUTR-23 GREY 29L COMM OUS, VLV EVOLUTR-23 TAV EVOLUT R CE 7L MX, VLV EVOLUTR-23 TAV EVOLUT R CE 26L MX, VLV EVOLUTR-23 TAV CA 2Y MX, VLV EVOLUTR-23 GREY 6L COMM OUS, VLV EVOLUTR-23-US TAV 23 US COMM MX; b. EVOLUTR-23-C, Labeled as VLV EVOLUTR-23-C TAV EVOLUT R US IDE

Medtronic Heart Valves Division

FDA Devices Moderate Dec 16, 2020

Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport inside and outside of the hospital environment.

Philips North America Llc

FDA Devices Moderate Dec 16, 2020

MassChrom Amino Acid Analysis Plasma Control Level II, Order No. 0472 - Product Usage: The kit is intended for amino acid metabolic screening, confirmation of a tentative diagnosis, and monitoring of treatment in individuals diagnosed with a metabolic disorder.

Chromsystems Instruments & Chemicals GmbH

FDA Devices Moderate Dec 16, 2020

Randox Rx Series Mg - Product Usage: For the quantitative in vitro determination of Magnesium in serum, plasma and urine Catalogue Number: MG8326

Randox Laboratories Ltd.

FDA Devices Moderate Dec 16, 2020

Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is easy to install and to use.

Spacelabs Healthcare, Ltd.

CPSC No agency class Dec 16, 2020

BRP Recalls Can-Am Screw Jacks Due to Crush Hazard

CPSC No agency class Dec 16, 2020

Camp Chef Recalls Portable Gas Stoves Due to Fire Hazard

CPSC No agency class Dec 16, 2020

Cycling Sports Group Recalls Cannondale Canvas NEO Bicycles Due to Fall Hazard

CPSC No agency class Dec 16, 2020

Graco Recalls Inclined Sleeper Accessory Included with Four Models of Playards to Prevent Risk of Suffocation

CPSC No agency class Dec 16, 2020

LG Energy Solution Michigan Recalls Home Energy Storage Batteries Due to Fire Hazard

NHTSA No agency class Dec 16, 2020

AUDI 2020: SERVICE BRAKES, HYDRAULIC:PEDALS AND LINKAGES

AUDI

NHTSA No agency class Dec 16, 2020

VOLKSWAGEN 2012-2014: AIR BAGS:FRONTAL

VOLKSWAGEN

NHTSA No agency class Dec 15, 2020

VOLVO 2021: SERVICE BRAKES, HYDRAULIC:CRITICAL FASTENERS

VOLVO

NHTSA No agency class Dec 11, 2020

MERCEDES-BENZ 2018-2020: ELECTRICAL SYSTEM:STARTER ASSEMBLY

MERCEDES-BENZ

NHTSA No agency class Dec 11, 2020

MERCEDES-BENZ 2020: EXTERIOR LIGHTING:HEADLIGHTS

MERCEDES-BENZ

NHTSA No agency class Dec 11, 2020

MERCEDES-BENZ 2019: STRUCTURE:BODY:HOOD

MERCEDES-BENZ

NHTSA No agency class Dec 11, 2020

PORSCHE 2000-2008: SUSPENSION:FRONT:MACPHERSON STRUT

PORSCHE

CPSC No agency class Dec 10, 2020

Homfa Cabinets Recalled Due to Tip-Over and Entrapment Hazards; Made by Shenzhen Luosi Ge Trading Co. (Recall Alert)

Shenzhen Luosi Ge Trading Co., of China (owner of Homfa trademark)

CPSC No agency class Dec 10, 2020

Scentsy Recalls Electrical Oil Warmers Due to Fire Hazard (Recall Alert)

CPSC No agency class Dec 10, 2020

Thermo Tents Recalls Mór Series Tents Due to Fire Hazard; Tents are Mislabeled as Fire Retardant (Recall Alert)

NHTSA No agency class Dec 10, 2020

HONDA 2018-2020: ELECTRICAL SYSTEM:BODY CONTROL MODULE:SOFTWARE

HONDA

NHTSA No agency class Dec 10, 2020

ACURA,HONDA 2007-2015: POWER TRAIN:DRIVELINE:DRIVESHAFT

ACURA,HONDA

NHTSA No agency class Dec 10, 2020

HONDA 2013-2015: POWER TRAIN:DRIVELINE:DRIVESHAFT

HONDA

NHTSA No agency class Dec 10, 2020

HONDA 2002-2006: VISIBILITY:POWER WINDOW DEVICES AND CONTROLS

HONDA

NHTSA No agency class Dec 10, 2020

SUBARU 2020: BACK OVER PREVENTION:DISPLAY FUNCTION

SUBARU

NHTSA No agency class Dec 10, 2020

FORD 2005-2021: STEERING

FORD

FDA Food Moderate Dec 9, 2020

YAGUMO AMANATTO GIFT BOX 6P 6/19.01 OZ JAN Code: 49 03089 39050 4 Imported by JFC International Inc. Los Angeles, CA 90040

J F C International Inc

FDA Food Moderate Dec 9, 2020

Lemonade 1/2 gallon glass bottle. UPC:7525200265. "10% Real Juice Lemonade"

Homestead Creamery, Inc.

FDA Food Moderate Dec 9, 2020

Dole Brands, Savory Spinach Dijon, 4.9 oz,

Sunnyside Farms

FDA Food Critical Dec 9, 2020

Tanimura & Antle brand Romaine lettuce. 1 head 12,15,018 and 24 case Product of USA UPC: 2-27918 20314-9 Tanimura & Antle, Salinas, CA

Tanimura & Antle

FDA Food Critical Dec 9, 2020

Dole" Organic Romaine Hearts 3pk Organic Biologique) (UPC 0-71430-90061-1), Wild Harvest Organic Romaine Hearts, Net Wt 12 oz. (UPC 7-11535-50201-2),

Dole Fresh Vegetables Inc

FDA Food Moderate Dec 9, 2020

Minute Maid STRAWBERRY LEMONADE FLAVORED WITH OTHER NATURAL FLAVORS 59 FL OZ (1.8 QT) 1.75 L PRODUCED FOR THE COCA-COLA COMPANY ATLANTA, GA Unit UPC 0 25000 01970 8 Case UPC 000-25000-04812-8

The Coca-Cola Company

FDA Food Critical Dec 9, 2020

Quantum Health branded Elderberry liquid herbal extract dietary supplement is packaged in 2oz glass bottle, 12 bottles/case. Product is shelf stable with net wt. 2 fl oz/59 mL. UPC code: 0 46985 01625 4 Product is distributed by Quantum, Inc., Eugene, OR.

Quantum Inc

FDA Food Low Dec 9, 2020

BELLEFONTAINE PEANUT BUTTER & BROWNIES DAIRY FREE FROZEN DESSERT 1 PINT (473 ML) packaged in paper cup

BLISS TEXAS

FDA Food Moderate Dec 9, 2020

Minute Maid WATERMELON FLAVORED FRUIT DRINK WITH OTHER NATURAL FLAVORS 59 FL OZ (1.8 QT) 1.75 L PRODUCED FOR THE COCA-COLA COMPANY ATLANTA, GA Unit UPC 0 25000 04811 1, Case UPC 000-25000-04812-8

The Coca-Cola Company

FDA Food Moderate Dec 9, 2020

Tucson Tamale Blue Corn & Veggie Tamales (2 Pack), 11 OZ (312g), plastic bag, UPC 8 53437 00234, Keep Frozen, 6 packs/box (case)

Tucson Tamale Wholesale Company, LLC

FDA Food Moderate Dec 9, 2020

Tucson Tamale Blue Corn, Veggie & Cheese Tamales (2 Pack), 11 OZ (312g), plastic bag, UPC 8 53437 00233, Keep Frozen, 6 packs/box (case)

Tucson Tamale Wholesale Company, LLC

FDA Food Moderate Dec 9, 2020

Pacific Jade Indian Curry Sauce Starter With Fenugreek and Cardamom, wholesale case with 2, 39 oz. plastic tubs, case UPC 50758108742487

CELTRADE CANADA

FDA Drug Critical Dec 9, 2020

Anagrelide Capsules, USP 1 mg, 100 capsules, Rx only, Manufactured in India for: Torrent Pharma Inc., Basking Ridge, NJ 07920 NDC 13668-462-01

Torrent Pharma Inc

FDA Drug Moderate Dec 9, 2020

ARIPIPRAZOLE TABLETS, 15 mg, 30-count. bottles, Rx Only, GSMS Incorporated, Manufactured by: Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS, Incorporated, Camarillo, CA 93012 USA, NDC #60429-449-30

Golden State Medical Supply 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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2020

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 2020 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.