PlainRecalls

2020 Recalls

5,998 recalls · Page 52 of 120

2020 Recall Year Insight

Federal agencies issued 5,998 product recalls indexed by PlainRecalls in calendar year 2020. That represents about 5.90% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 16.4 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 120 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 23 critical, 26 moderate, and 1 lower-severity recalls. The page references 8 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 Critical Jul 22, 2020

BodyGuard Microset, REF: A100-163XSL

CME America, LLC

FDA Devices Critical Jul 22, 2020

Standard BodySet with Needleless Connectors, REF: A120-125XS

CME America, LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset with Male Luer Connectors, REF: A100-163XEBF

CME America, LLC

FDA Devices Moderate Jul 22, 2020

SKAFFOLD CMF IMPRESS (MP), 5CC. Product Number: CMMP-IM05, UDI: 813845020689 - Product Usage: Callos is indicated to fill bony voids or gaps of the …

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

SKAFFOLD FLOW, 3CC and SKAFFOLD FLOW (MX) 3CC. Product Number: SKMX-FL03, UDI: 813845020887 - Product Usage: Callos is indicated to fill bony voids …

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

OSTEOVATION, 10CC, INJECT FORMULA. Product Number: 390-2010, UDI: 813845020061 - Product Usage: Callos is indicated to fill bony voids or gaps of th…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT C, 5CC. Product Number: C-C5CC, UDI: 813845021112 - - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal sys…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Mucocutaneous Swabs Product Usage: is intended for use on the LIAISON MDX instrument …

DiaSorin Molecular LLC

FDA Devices Moderate Jul 22, 2020

OSTEOVATIONEX 2CC INJECT FORMULA. Product Number: 390-0002, UDI: 813845020009 - Product Usage: Callos is indicated to fill bony voids or gaps of the…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset with Filter, REF: A100-164XESF

CME America, LLC

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT C, 3CC. Product Number: C-C3CC, UDI: 813845021105 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal syste…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A100-163XE90S

CME America, LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-003XS2YV

CME America, LLC

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT C, 10CC. Product Number: C-C10CC, UDI: 813845021129 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal sys…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT FLOW, OUS, 5CC Product Number: C-FLOW5CC-OUS, UDI: 813845020351 - Product Usage: Callos is indicated to fill bony voids or gaps of the …

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer, REF: A120-160XYBF

CME America, LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-112XSFK

CME America, LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-160XYSF

CME America, LLC

FDA Devices Moderate Jul 22, 2020

DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre…

Neocis Inc.

FDA Devices Moderate Jul 22, 2020

MEDTRONIC BONE VOID FILLER, SMALL. Product Number: C07A, UDI: 813845020504 - Product Usage: Callos is indicated to fill bony voids or gaps of the sk…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A100-163XESV

CME America, LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset with Filter, REF: A100-163XESF

CME America, LLC

FDA Devices Critical Jul 22, 2020

CMExpress Microbore Set, REF: A120-160C

CME America, LLC

FDA Devices Critical Jul 22, 2020

CMExpress Microbore Set, REF: A120-160CRV

CME America, LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset with Needleless Adaptor, REF: A120-003XSNY

CME America, LLC

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT, CMF IMPACT, 5CC, Product Number: C-CMF5CC, UDI: 813845020948 - Product Usage: Callos is indicated to fill bony voids or gaps of the sk…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-160XPS

CME America, LLC

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT, FLOW 5CC. Product Number: C-FLOW5CC, UDI: 813845020337 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

MagNA Pure 96 Instrument, clinical sample concentrator, Material number 06541089001 - Product Usage: This protocol is intended for pipetting samples…

Roche Molecular Systems, Inc.

FDA Devices Moderate Jul 22, 2020

OSTEOVATIONEX, INJECT 3CC. Product Number: 390-0003, UDI: 813845020016 - Product Usage: Callos is indicated to fill bony voids or gaps of the skelet…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-160GCFA

CME America, LLC

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT FLOW, 10CC. Product Number: C-FLOW10CC, UDI: 813845020368 - - Product Usage: Callos is indicated to fill bony voids or gaps of the skel…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

CMExpress Needleless Y Site Microbore Set, REF: A120-160CYNVK

CME America, LLC

FDA Devices Moderate Jul 22, 2020

OSTEOVATION, 3CC, IMPACT FORMULA. Product Number: 390-2103, UDI: 813845020078 - Product Usage: Callos is indicated to fill bony voids or gaps of the…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

SKAFFOLD RENU FLOW, 10CC. Product Number: SKMA-FL10, UDI: 813845020856 - Product Usage: Callos is indicated to fill bony voids or gaps of the skelet…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

SK SKAFFOLD IMPRESS 10CC. Product Number: SKAF-IM10, UDI: 813845020795 - Product Usage: Callos is indicated to fill bony voids or gaps of the skelet…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-161XYB

CME America, LLC

FDA Devices Moderate Jul 22, 2020

OSTEOVATION, 5CC, INJECT FORMULA. Product Number: 390-2005, UDI: 813845020054 - Product Usage: Callos is indicated to fill bony voids or gaps of the…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A100-163XSFL

CME America, LLC

FDA Devices Critical Jul 22, 2020

CMExpress Microbore Set, REF: A120-161CYF

CME America, LLC

FDA Devices Moderate Jul 22, 2020

This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product Usage: are intended to be used …

DJO, LLC

FDA Devices Moderate Jul 22, 2020

ACUMED IMPACT 10CC. Product Number: 65-0110-S, UDI: 813845020269 - Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extre…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

MOL3650 Simplexa VZV Direct - Product Usage: is intended for use on the LIAISON MDX instrument for the qualitative detection of varicella-zoster viru…

DiaSorin Molecular LLC

FDA Devices Moderate Jul 22, 2020

ACUMED IMPACT 5CC. Product Number: 65-0105-S, UDI: 813845020252 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal syst…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

DRW-0742-01: Gen 2 Anterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-…

Neocis Inc.

FDA Devices Low Jul 22, 2020

POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Extended Dwell Catheter made of ChronoFlex C with BioGUARD Technology), Catalog No. 9410…

Access Scientific LLC

FDA Devices Critical Jul 22, 2020

CMExpress Microbore Sets, REF: A120-160C2YRV

CME America, LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-125XSE

CME America, LLC

FDA Devices Moderate Jul 22, 2020

enVista one-piece hydrophobic acrylic toric intraocular lens, Bausch and Lomb - Product Usage: is indicated for primary implantation in the capsular …

Bausch & Lomb Surgical, Inc.

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A100-163XES

CME America, LLC

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2020 across the FDA, CPSC 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 July 2026.