PlainRecalls

2020 Recalls

4,819 recalls · Page 59 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 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, NHTSA, or USDA FSIS 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

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

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 2019-2020: SEAT BELTS:FRONT:RETRACTOR

FORD

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.

FDA Devices Moderate Apr 29, 2020

Temperature Sensing 100% Silicone Foley Catheter, Part Number 102201100880MD - Product Usage: is a 3 lumen silicone catheter with a sensor to measure…

Degania Medical Devices Pvt. Ltd.

FDA Devices Moderate Apr 29, 2020

ClearCanvas RIS/PACS

Synaptive Medical Inc

FDA Devices Moderate Apr 29, 2020

Olympus Pleuravideoscope, Model LTF-160

Olympus Corporation of the Americas

FDA Devices Moderate Apr 29, 2020

Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN: M006175263110

Boston Scientific

FDA Devices Moderate Apr 29, 2020

Polaris Ultra Ureteral Stent Set 6FX24CM with .035 Sensor UPN: M006192132080

Boston Scientific

FDA Devices Moderate Apr 29, 2020

Sensor Nitinol Wire with Hydrophilic Tip .0383CM FLEX ANG/150CM UPN: M0066703101 box 5 UPN: M0066703100 single unit

Boston Scientific

FDA Devices Moderate Apr 29, 2020

Medivators Endo carry-on Procedure Kit REF CPK-100222-0002 - Product Usage: is intended to be used with an air or CO2 source and/or a pump along wit…

Medivators, Inc.

FDA Devices Moderate Apr 29, 2020

Medivators EndoGator REF 100651. Kit for Olympus 140/160/180/190 Series GI Endoscopes for CO2 Connection with Endogator EGP-100, Olympus OFP, Olympu…

Medivators, Inc.

FDA Devices Moderate Apr 29, 2020

Fentanyl Reagent Kit, Product N. CC444, Contains: FENT R1 Reagent and FENT R2 Reagent

Carolina Liquid Chemistries Corp

FDA Devices Moderate Apr 29, 2020

ABL90 FLEX PLUS Analyzer, Model Number 393-092 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care set…

Radiometer Medical ApS

FDA Devices Moderate Apr 29, 2020

Sensor Nitinol Wire with Hydrophilic Tip .035 3CM FLEX /150CM UPN: M0066703061 box 5 UPN: M0066703060 single unit

Boston Scientific

FDA Devices Moderate Apr 29, 2020

The VITEK 2 Gram-positive Susceptibility Card is intended for use with the VITEK 2 Systems in clinical laboratories as an in-vitro test to determine …

Biomerieux Inc

FDA Devices Moderate Apr 29, 2020

ABL90 FLEX Analyzer, Model Numbers 393-090, with software versions below 3.4MR2 - Product Usage: It is intended for use in a laboratory environment, …

Radiometer Medical ApS

FDA Devices Moderate Apr 29, 2020

Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips, Model Number 110028522 - Product Usage: Intended to be used in surgery to reli…

Biomet, Inc.

FDA Devices Moderate Apr 29, 2020

Stretch VL Ureteral Stent Set 6FX22- 30CM with .035 Sensor UPN: M006185156080

Boston Scientific

FDA Devices Moderate Apr 29, 2020

Smith & Nephew FOOTPRINT Ultra PK Suture Anchor, 5.5mm Part Number: 72202902

Smith & Nephew, Inc.

FDA Devices Moderate Apr 29, 2020

Temperature Sensing 100% Silicone Foley Catheter, Part Number 102201101063MD - Product Usage: is a 3 lumen silicone catheter with a sensor to measure…

Degania Medical Devices Pvt. Ltd.

FDA Devices Moderate Apr 29, 2020

TCM4 Base unit, Ref 391-880, UDI:(01)05700693918808, used with the monitor modules TCM4 (902-778), TCM40 (902-778, 902-946 or 902-862), TCM400 (902-5…

Radiometer Medical ApS

FDA Devices Moderate Apr 29, 2020

Fresenius 2008T Hemodialysis Machine: Part Number Description 190573 2008T HEMODIAL YSIS SYS. OLC/DIASAFE PLUS; 190713 2008T HEMODIAL YSIS SYS., w…

Fresenius Medical Care Holdings, 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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2020