PlainRecalls

2020 Recalls

5,939 recalls · Page 109 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 50 records, severity classification shows 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 22 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 Devices Moderate Feb 5, 2020

SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resolu…

GE Healthcare, LLC

FDA Devices Moderate Feb 5, 2020

GIBSON Healthcare Membrane Extended, 15mm x 20mm, Reference Number 5303-306 - - Product Usage: Indicated for use in oral surgical procedures as a res…

Collagen Matrix Inc

FDA Devices Moderate Feb 5, 2020

LEGION AP Cutting Block Size 4, REF 71434409; LEGION AP Cutting Block Size 6, REF 71434411; LEGION AP Cutting Block Size 7, REF 71434412; LEGION A…

Smith & Nephew, Inc.

FDA Devices Moderate Feb 5, 2020

VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

GIBSON Healthcare Membrane 6-9, 15mm x 20mm, Reference Number 5303-226 - Product Usage: Indicated for use in oral surgical procedures as a resorbable…

Collagen Matrix Inc

FDA Devices Moderate Feb 5, 2020

Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide

Arthrex, Inc.

FDA Devices Moderate Feb 5, 2020

Brasseler USA KM169-39-76 Steinmann Pin Single Diamond Smooth, Diameter 2.8 mm, Length 228 mm Product Usage: A Steinmann Pin is used for internal…

Brasseler USA I Lp

FDA Devices Moderate Feb 5, 2020

GIBSON Healthcare Membrane 6-9, 30mm x 40mm, Reference Number 5303-299 - Product Usage: Indicated for use in oral surgical procedures as a resorbable…

Collagen Matrix Inc

FDA Devices Moderate Feb 5, 2020

Japan CS Elite FASTPACK DISP. SET - 125ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subs…

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

VitreQ 23G PFC Injection Needle- Ref: MD23.D01 GTIN: 8719214221362

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

Atellica CH 930 Analyzer, Siemens Material Number 11067000, Software Versions V1.19.2 or 1.20.0 The Atellica CH 930 Analyzer is an automated, cli…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Feb 5, 2020

Cyberonics VNS Therapy AspireSR, Model 106 Generator, 26-0007-8400/1. The firm name on the label is CYBERONICS, INC., Houston, TX. Vagus nerve sti…

LivaNova USA Inc

FDA Devices Moderate Feb 5, 2020

VitreQ 25G Silicone Tipped Cannula-REF: CN25.D01 GTIN: 8719214221522

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resoluti…

GE Healthcare, LLC

FDA Devices Moderate Feb 5, 2020

SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resoluti…

GE Healthcare, LLC

FDA Devices Moderate Feb 5, 2020

Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire .035"; Recommended Introduce…

Bard Peripheral Vascular Inc

FDA Devices Moderate Feb 5, 2020

CS Elite Processing Set (225 ml) Autotransfusion Device - Product Usage:its related accessory components are intended for use to recover blood shed d…

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

Exactech equinoxe PLATFORM FRACTURE, HUMERAL STEM, CEMENTED, Right, 6.5mm, REF 304-22-07 - Product Usage: The Equinoxe Shoulder System is indicated f…

Exactech, Inc.

FDA Devices Moderate Feb 5, 2020

iQ200 Series Urine Microscopy Analyzer, Catalog numbers: 700-3345, 700-3375, 700-3325, 700-3347, 700-3300RFB, 700- 3320, 700-3320RFB, 700-3322, 700-…

Beckman Coulter Inc.

FDA Devices Moderate Feb 5, 2020

(1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G BF Brush Needles-BF25.D52 GTIN: 8719214221188

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE, Part Number 04.210.116TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver si…

Synthes, Inc.

FDA Devices Moderate Feb 5, 2020

VitreQ 25G PFC Injection Needle-Ref: MD25.D01 GTIN: 8719214221386

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

CS Elite Fastpack, 225 mL, 20¿ Res Autotransfusion Device - Product Usage: its related accessory components are intended for use to recover blood she…

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

CS5/5+ Bowl Kit-125 mL Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processi…

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

Medline DYNDA1928 VP TRAY WITH PVP Packaged in Mexico GLOVE:Made in Malaysia APPLICATOR:Made in China STERILE (01)40889942587583(10)0000000000 …

Medline Industries Inc

FDA Devices Moderate Feb 5, 2020

Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14

Johnson & Johnson Surgical Vision Inc

FDA Devices Moderate Feb 5, 2020

VitreQ 25G Pick Needles-REF: CN25.D04 GTIN: 8719214221607

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery …

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

VitreQ 23G Silicone Tipped Cannula-CN23.D01 GTIN: 8719214221508

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0.

RAYSEARCH LABORATORIES AB

FDA Devices Moderate Feb 5, 2020

GIBSON Healthcare Membrane 6-9, 20mm x 30mm, Reference Number 5303-235 - Product Usage: Indicated for use in oral surgical procedures as a resorbable…

Collagen Matrix Inc

FDA Devices Moderate Feb 5, 2020

GIBSON Healthcare Membrane Extended, 30mm x 40mm, Reference Number 5303-342 - Product Usage: Indicated for use in oral surgical procedures as a resor…

Collagen Matrix Inc

FDA Devices Moderate Feb 5, 2020

EQ-400-RH-QZ and EQ-400-LH-BK products Product Usage: The device is a very broadband light source emitting incoherent non-laser light from the D…

Energetiq Technology Inc

FDA Devices Moderate Feb 5, 2020

JAPAN CS ELITE FASTPACK, 225ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to a…

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

Japan DISP SET, 263J, 205J, 208 - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood sh…

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

BA-800M Chemistry Analyzer Part Numbers BA81E-PA00002 and BA81E-PA00003, Containing Gas spring YQ-8/18-90-272-180N (Material Code M6T-010001--- (fron…

Mindray DS USA, Inc. dba Mindray North America

FDA Devices Moderate Feb 5, 2020

2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE, Part Number 04.210.112TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver si…

Synthes, Inc.

FDA Devices Moderate Feb 5, 2020

Custom Healthcare Systems, Inc. Inpatient Dialysis Kit PAK-19244. Single use. Dialysis kit

Custom Healthcare Systems, Inc.

FDA Devices Moderate Feb 5, 2020

VitreQ 25G Blunt Needles with luer-lock connector-REF : CN25.D05 GTIN: 8719214221645

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

CS5/5+ Fastpacks, 125 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery …

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgical i…

Zimmer Biomet, Inc.

FDA Devices Moderate Feb 5, 2020

VitreQ 27G VFI Cannula-REF: CN27.D03 GTIN: 8719214221461

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

CS Elite Processing Set (125 ml) Autotransfusion Device - Product Usage:its related accessory components are intended for use to recover blood shed d…

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

Cyberonics VNS Therapy AspireHC Model 105 Generator, 26-0007-4000/3. The firm name on the label is CYBERONICS, INC., Houston, TX. Vagus nerve stim…

LivaNova USA Inc

FDA Devices Moderate Feb 5, 2020

SIGNA Vibrant Nuclear Magnetic Resonance Imaging System, 1.5T Signa HDx, 1.5T Signa HDxt, Signa HDi - Product Usage: is a whole body magnetic resonan…

GE Healthcare, LLC

FDA Devices Moderate Feb 5, 2020

High Speed Cell Saver¿5/5+ Bowl Set Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery…

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

JAPAN CELL SAVER ELITE SET - 125ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent …

Haemonetics Corporation

FDA Devices Moderate Feb 5, 2020

(1) VitreQ 20G BF Blunt Needles-Ref: BF20.D51 GTIN: 8719214221089 (2) VitreQ 20G BF Brush Needles-REF: BF20.D52 GTIN: 8719214221102

Vitreq Bv

FDA Devices Moderate Feb 5, 2020

Cobas infinity central lab / cobas infinity core license-a Calculator/Data Processing Module, For Clinical Use Material Number: 07154003001

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Feb 5, 2020

The da Vinci SP surgical system is made of three main components: the Surgeon Console (SC), the Vision Cart (VC), and the Patient Cart (PC). The Pati…

Intuitive Surgical, 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