PlainRecalls

2020 Recalls

4,819 recalls · Page 58 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, 35 moderate, and 4 lower-severity recalls. The page references 35 distinct recalling firms operating in 6 distinct product categories, with 41 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (27), NHTSA (9), FDA Food (7), 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 13, 2020

Transducer S7-3t UDI (01)00884838061439 REF 989605406772 Can be used with: CX50, EPIQ 7, Affiniti 50 and Affiniti 70 Ultrasound systems - Prod…

Philips Ultrasound Inc

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175828P0 - Product Usage: for use in the replacement or repair …

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 - Product Usage: The Epimed RF Int…

Epimed International

FDA Devices Moderate May 13, 2020

Transducer S8-3t UDI (01)00884838067523 REF 989605420183 Can be used with: iE33 Utrasound System - Product Usage: Diagnostic ultrasound imagin…

Philips Ultrasound Inc

FDA Devices Moderate May 13, 2020

R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124; REF/UDI: 257-2010D(01)00818788022127 - Product Usage:The Epimed RF Intr…

Epimed International

FDA Devices Moderate May 13, 2020

Delfi Medical Innovations, VariFit Contour Cuffs, single use adult thigh cuff, single port, single bladder, REF 9-9300-003. Rx Only, Sterile

Delfi Medical Innovations, Inc.

FDA Devices Moderate May 13, 2020

Gentell Honey Hydrogel Hydrogel 4oz. Tube. Wound dressing containing hydrogel and honey (100% Leptospermum honey), Model Number: GEN-11340 - Produc…

Gentell, Inc

FDA Devices Moderate May 13, 2020

System AXIOM Aristos FX - Product Usage: A dedicated x-ray system with a flat panel detector which allows the acquisition of x-ray exposures without …

Siemens Medical Solutions USA, Inc

CPSC Moderate May 13, 2020

Hodedah Recalls HI4DR 4-Drawer Chests Due to Tip-Over and Entrapment Hazards; Remedies May Be Delayed Due to COVID-19 Restrictions; Keep Product Away…

NHTSA Critical May 13, 2020

AUDI 2020: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

AUDI

NHTSA Critical May 13, 2020

AUDI 2019: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

AUDI

NHTSA Critical May 13, 2020

AUDI 2020: POWER TRAIN:AUTOMATIC TRANSMISSION:COOLING UNIT AND LINES

AUDI

NHTSA Critical May 13, 2020

PORSCHE 2020: POWER TRAIN:AUTOMATIC TRANSMISSION:COOLING UNIT AND LINES

PORSCHE

NHTSA Critical May 8, 2020

FORD 2019-2020: POWER TRAIN:AUTOMATIC TRANSMISSION:GEAR POSITION INDICATION (PRNDL)

FORD

NHTSA Critical May 8, 2020

FORD,LINCOLN 2020: ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL

FORD,LINCOLN

NHTSA Critical May 8, 2020

INTERNATIONAL 2019-2020: EQUIPMENT:MECHANICAL:WRECKER AND WHEEL LIFT DEVICES

INTERNATIONAL

NHTSA Critical May 8, 2020

FORD 2014-2017: VISIBILITY:SUN/MOON ROOF ASSEMBLY

FORD

CPSC Moderate May 7, 2020

Fully Popped Recalls Poppin' Cobs 10 Pack Microwave Popcorn Due to Fire and Burn Hazards; Sold Exclusively at Uncommon Good Stores

Gilchrist Bag Manufacturing LLC, of Camden, Arizona

CPSC Moderate May 7, 2020

Noah Clothing Recalls Men's Reverse Fleece Hoodies Due to Violation of Federal Flammability Standard; Burn Hazard

CPSC Moderate May 7, 2020

Sobeauty Recalls "Mag Cube" Magnetic Ball Sets Due to Risk of Ingestion by Children That Could Cause Serious and Permanent Intestinal Injuries or Dea…

NHTSA Critical May 7, 2020

INTERNATIONAL 2018-2020: ENGINE

INTERNATIONAL

FDA Food Low May 6, 2020

XinXing Dried Plum, Net Wt. 5.3 oz.(150g)

Rong Shing Trading NY Inc

FDA Food Low May 6, 2020

Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition

GOLDEN NUTRITION INC

FDA Food Critical May 6, 2020

Whole Foods Market Minestrone Soup PLU code printed on the product scale labels beginning with 248529 for soup sold in clear plastic deli-style conta…

Whole Foods Market

FDA Food Moderate May 6, 2020

7075931 Flounder Stuffed W/ Seafood FRZN, Net Wt LBS 15.00 (6.80 KG), 20 packages per case

Freedman Food Service, Inc dba Buckhead Meat & Seafood of Houston

FDA Food Moderate May 6, 2020

5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink

Ocean Spray Cranberries Inc.

FDA Food Moderate May 6, 2020

Tops Mint Flavor Pure Dark Chocolate 45% Cocoa NET WT 3.5 oz.(100g)

Tops Markets Inc.

FDA Food Low May 6, 2020

CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL

Alfa Vitamins Laboratories, Inc.

FDA Drug Moderate May 6, 2020

Nizatidine Oral Solution, 15 mg/mL (75 mg/5mL) USP 480 mL bottles, Rx Only Distributed by: Gemini Laboratories, LLC Bridgewater, NJ 08807 NDC 60846-3…

Amneal Pharmaceuticals of New York, LLC

FDA Drug Critical May 6, 2020

Ceftazidime for Injection USP and Dextrose for Injection USP, 2 g, 50 mL Duplex Container, RX only, B Braun Medical Inc., Bethlehem, PA 18018-3524, N…

B. Braun Medical Inc

FDA Drug Low May 6, 2020

Esomeprazole Magnesium Delayed Release Capsules USP, 40 mg*, 1000-count bottles, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited Bachupally - 500…

Dr. Reddy's Laboratories, Inc.

FDA Devices Moderate May 6, 2020

X12+ and patient cable for the X12+ Telemeter with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP, PAT CBL 10WIRE LEADFORM IEC SNAP, PAT…

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

MoXy Laser Fiber, Material Number 0010-2400 - Product Usage: The fiber can be used for the surgical incision/excision, vaporization, ablation, hemost…

Boston Scientific Corporation

FDA Devices Moderate May 6, 2020

Philips Azurion 7 M20 -XperGuide Software hosted in Interventional Workspot 1.5 when used with the Azurion R2.0 system Interventional fluoro…

Philips North America, LLC

FDA Devices Moderate May 6, 2020

Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI 280, ELI 380, R-Scribe and Con…

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor under the following device names: PAT CBL 10WIRE AHA SNAP JSCREW, PAT CBL 10WIRE I…

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

Prismaflex System, Prismaflex Control Unit

Baxter Healthcare Corporation

FDA Devices Moderate May 6, 2020

ProACT Implantation Instrument Set, is a reusable, steam sterilizable surgical instrument set consisting of a U-Channel Sheath through which the Pro …

Uromedica Inc.

FDA Devices Moderate May 6, 2020

Lunar iDXA bone densitometer

GE Healthcare, LLC

FDA Devices Moderate May 6, 2020

Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer

GE Healthcare, LLC

FDA Devices Moderate May 6, 2020

Prismaflex System, Prismaflex Control Unit

Baxter Healthcare Corporation

FDA Devices Moderate May 6, 2020

Neptune E-SEP 165mm Blade Electrode, Catalog Number 0703-165-001 - Product Usage: The Neptune E-SEP is an Integrated Smoke Evacuation Pencil (pencil)…

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate May 6, 2020

ViewRay System: Model No. 10000 and 20000 for radiation treatment. PN11440 MRIdian System Treatment Planning and Delivery System (TPDS) software

Viewray, Inc.

FDA Devices Moderate May 6, 2020

Replaceable lead set for the Wireless Acquisition Module (WAM), which is the ECG front-end for various Electrocardiographs. Sold under the followin…

WELCH ALLYN, INC/MORTARA

FDA Devices Moderate May 6, 2020

PreludeSYNC DISTAL Radial Compression Devices, SDRB-REG-LT, SDRB-REG-RT

Merit Medical Systems, Inc.

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.

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