2020 Recalls
4,819 recalls · Page 70 of 97
2020 Recall Year Insight
Federal agencies issued 4,819 product recalls indexed by PlainRecalls in calendar year 2020. That represents about 5.74% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 13.2 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 97 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 11 critical, 39 moderate, and 0 lower-severity recalls. The page references 28 distinct recalling firms operating in 6 distinct product categories, with 34 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (25), NHTSA (11), CPSC (11), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.
D-0014 3COR 14MM DISTRACTION SCREWS, 5/BOX, STERILE - Product Usage: The 3COR Distraction Screws and the TSI Quick Start Distraction Screws products …
TeDan Surgical Innovations LLC
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multip…
Avid Medical, Inc.
Artis Q Biplane, Model No. 10848282; Artis Q Ceiling, Model No.10848281; Artis Q Floor, Model No. 10848280; Artis Q zeego, Model No. 10848283 Pro…
Siemens Medical Solutions USA, Inc
COLUMBUS CRA/PSA TIB.PLAT.CEMENTED, Knee implant components, various sizes, model nos. NN469K NN470K NN471K NN472K NN473K NN474K NN475K NN476…
Aesculap Implant Systems LLC
COLUMBUS CR/PS TIB.PLAT.PLASMAPORE, Knee implant components, various sizes, model nos. NN081K NN082K NN083K NN084K NN085K NN086K NN087K NN088…
Aesculap Implant Systems LLC
OmniDiagnost Eleva System codes 708028 708027
Philips North America, LLC
Boston Scientific, LATITUDE Programming System, Model 3300 - Product Usage:The Boston Scientific LATITUDE Programming System is intended for use in h…
Boston Scientific Corporation
Teleflex Pilling Aortic Punch, 4.0mm. Sterile, Rx Only, disposable. Included as part of Intl-Cardiac Surgery Kit - Product Usage: This device is use…
Deroyal Industries, Inc. Lafollette
IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use with the IMMULITE systems Ana…
Siemens Healthcare Diagnostics, Inc.
Ysio, model no. 10281013 Product Usage: The product is a stationary X-Ray system.
Siemens Medical Solutions USA, Inc
Stryker, REF: 0250070450, 5.0 mm x 45 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Sterile, CE, UDI: (01) 07613327051926 This products …
Stryker Corporation
Integris Allura 15 & 12, monoplane (system code 722043) and biplane (system code 722044)
Philips North America, LLC
CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and CMExpress
CME America, LLC
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multip…
Avid Medical, Inc.
HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M35…
Philips North America, LLC
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multip…
Avid Medical, Inc.
MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038
Philips North America, LLC
Poly G Integris H5000, System code 72246
Philips North America, LLC
DS-0022 QUICK START DISTRACTION SCREW 12MM 5/BOX STERILE - Product Usage: These products are intended to be used by trained surgeons and are designed…
TeDan Surgical Innovations LLC
Rheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vitro diagnostic use, Product code: LK151.S.A. , UDI: 05051700018319
The Binding Site Group, Ltd.
TRUMATCH Orthognathics - Genioplasty Surgical Kit, Add-on, Catalog Number: SD980.013
Materialise N.V.
Low Profile Screw, 4.5 x 20 mm The Low Profile ScrewTM, 4.5 x 20 mm, AR-8545-20, is used with the Ankle Fusion Line of plates and is intended to p…
Arthrex, Inc.
AS COLUMBUS CR/PS TIB.PLAT.CEMENTED,Knee implant components, various sizes, model nos. NN058Z NN070Z NN071Z NN072Z NN073Z NN074Z NN075Z NN07…
Aesculap Implant Systems LLC
D-0012 3COR 12MM DISTRACTION SCREWS, 5/BOX, STERILE - Product Usage: The 3COR Distraction Screws and the TSI Quick Start Distraction Screws products …
TeDan Surgical Innovations LLC
COLUMBUS REV F TIBIA OFFSET CEMENTED, Knee implant components, various sizes, model nos. NR068K NR068Z NR070K NR070Z NR071K NR071Z NR072K NR0…
Aesculap Implant Systems LLC
FREIGHTLINER,MERCEDES-BENZ 2019: SERVICE BRAKES, AIR:SUPPLY:HOSES, LINES/PIPING, AND FITTINGS
FREIGHTLINER,MERCEDES-BENZ
FORD,LINCOLN 2014-2016: LATCHES/LOCKS/LINKAGES:DOORS:LATCH
FORD,LINCOLN
FREIGHTLINER 2020: POWER TRAIN:AXLE ASSEMBLY
FREIGHTLINER
FORD 2021: SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP
FORD
MERCEDES-BENZ 2018-2019: ENGINE
MERCEDES-BENZ
MERCEDES-BENZ 2020: STRUCTURE:FRAME AND MEMBERS
MERCEDES-BENZ
C3 Manufacturing Recalls Perfect Descent Climbing Systems Climbing Belay Devices Due to Fall Hazard
C3 Manufacturing LLC, of Littleton, Colo.
Children's Tool Kits Recalled by Grizzly Industrial Due to Violation of Federal Lead Content Ban and Toy Safety Requirements
Crate and Barrel Recalls Glass Pitchers Due to Laceration Hazard
Hawthorne Hydroponics Recalls Grower's Edge Vaporizers Due To Burn, Shock and Fire Hazard
Kawasaki USA Recalls Off-Highway Utility Vehicles Due to Crash Hazard (Recall Alert)
Kawasaki Motors Manufacturing Corp. U.S.A, of Lincoln, Neb.
Kawasaki USA Recalls Off-Highway Utility Vehicles Due to Fuel Leak, Fire Hazards (Recall Alert)
Kawasaki Motors Manufacturing Corp. U.S.A., of Lincoln, Neb.
Kids & Koalas Baby Walkers Recalled Due to Fall and Entrapment Hazards; Sold Exclusively on Amazon.com (Recall Alert)
Lilly of New York Children's Winter Boots Recalled by Kidz Concepts Due to Violation of Federal Lead Content Ban; Sold Exclusively at Zulily.com (Rec…
Wenzhou Jinlong Shoes Co., of China
Plant Therapy Recalls Wintergreen Essential Oils and Essential Oil Blends with Wintergreen Due to Failure to Meet Child Resistant Packaging Requireme…
Plant Therapy LLC, of Twin Falls, Idaho
Thule Recalls Thule Sleek Car Seat Adapters Due to Fall Hazard
Woom bikes USA Recalls Bicycles Due to Fall and Injury Hazards (Recall Alert)
BMW 2019-2020: SERVICE BRAKES, HYDRAULIC:FLUID
BMW
BMW 2020: POWER TRAIN:DRIVELINE
BMW
BMW 2020: SEAT BELTS:FRONT:BUCKLE ASSEMBLY
BMW
AUDI 2019-2020: ELECTRICAL SYSTEM:STARTER ASSEMBLY
AUDI
BMW 2019-2020: SERVICE BRAKES, HYDRAULIC:FLUID
BMW
Lindt Excellence 85% Cocoa Dark Chocolate Bars, 3.5 oz.(100g)
Lindt & Sprungli (USA), Inc.
Barts Ice Cream Co. brand of Chocolate Chip Cookie Dough ice cream (Vanilla ice cream with chunks of cookie dough and dark chocolate chips) packaged …
Snow's Acquisition, LLC
Kaiser Mild Banana Pepper Rings 1/4 KK in 1 gallon plastic bottles (4 gallons per case).
Kaiser Pickles LLC
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: CPSC + NHTSA + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2020
Read our methodology — how this data is sourced, computed, and verified.