PlainRecalls

2020 Recalls

4,819 recalls · Page 42 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 17 critical, 33 moderate, and 0 lower-severity recalls. The page references 6 distinct recalling firms operating in 2 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (49), FDA Drug (1), 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 Drug Moderate Jul 22, 2020

Carbamazepine 200 mg Tablets, 100-unit dose tablets per box, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-2489-00 for box;…

RemedyRepack Inc.

FDA Devices Moderate Jul 22, 2020

OSTEOVATION EX, 5CC, IMPACT FORMULA. Product Number: 390-0205, UDI: 813845020047 - Product Usage: Callos is indicated to fill bony voids or gaps of …

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

EXACTECH OSSILIX MP FIL, 10CC. Product Number: 662-02-10, UDI: 813845021051 - Product Usage: Callos is indicated to fill bony voids or gaps of the s…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT FLOW, OUS, 10CC. Product Number: C-FLOW10CC-OUS, UDI: 813845020382 - Product Usage: Callos is indicated to fill bony voids or gaps of t…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT FLOW, CAN, 5CC. Product Number: C-FLOW5CC-CAN, UDI: 813845020344 - Product Usage: Callos is indicated to fill bony voids or gaps of the…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

OSTEOVATIONEX 5CC, INJECT FORMULA. Product Number: 390-0005, UDI: 813845020023 - Product Usage: Callos is indicated to fill bony voids or gaps of th…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

OSTEOVATION, 5CC, IMPACT FORMULA. Product Number: 390-2105, UDI: 813845020085 - Product Usage: Callos is indicated to fill bony voids or gaps of the…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

OSTEOVATION RMX 10CC. Product Number: 390-6002, UDI: 813845021099 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal sy…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-161XPS

CME America, LLC

FDA Devices Moderate Jul 22, 2020

SKAFFOLD CMF IMPRESS (MP), 10CC. Product Number: CMMP-IM10, UDI: 813845020696 - 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 Female Luer, REF: A120-160XPSN

CME America, LLC

FDA Devices Moderate Jul 22, 2020

MEDTRONIC BONE VOID FILLER, LARGE. Product Number: C07B, UDI: 813845020511 - Product Usage: Callos is indicated to fill bony voids or gaps of the sk…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

DRW-0739-02: Gen 2 Posterior Chairside Splint LRUL (lower right-upper left) - Product Usage: intended to provide assistance in both the planning (pre…

Neocis Inc.

FDA Devices Moderate Jul 22, 2020

EXACTECH OSSILIX FIL (MX), 10CC. Product Number: 660-02-10, UDI: 813845021013 - - Product Usage: Callos is indicated to fill bony voids or gaps of t…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-160X2YB

CME America, LLC

FDA Devices Moderate Jul 22, 2020

ACUMED CALLOS INJECT 5CC. Product Number: 65-0005-S, UDI: 813845020238 - Product Usage: Callos is indicated to fill bony voids or gaps of the skelet…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard BodySet, REF: A120-160SAS

CME America, LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-160XSFK

CME America, LLC

FDA Devices Moderate Jul 22, 2020

EXACTECH OSSILIX FIL (MX), 5CC. Product Number: 660-02-05, UDI: 813845021006 - Product Usage: Callos is indicated to fill bony voids or gaps of the …

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT, CMF IMPACT, 3CC Product Number: C-CMF3CC, UDI: 813845020931 - Product Usage: Callos is indicated to fill bony voids or gaps of the ske…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

CMExpress Microbore Sets, REF: A120-161C

CME America, LLC

FDA Devices Moderate Jul 22, 2020

SKAFFOLD FLOW, 10CC. Product Number: SKMX-FL10, UDI: 813845020900 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal sy…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT, CMF IMPACT, 10CC, Product Number: C-CMF10CC, UDI: 813845020955 - 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: A120-160CYFRV

CME America, LLC

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT FLOW, 3CC. Product Number: C-FLOW3CC, UDI: 813845020320 - - Product Usage: Callos is indicated to fill bony voids or gaps of the skelet…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard set with Female Luer, REF: A120-003XSN

CME America, LLC

FDA Devices Moderate Jul 22, 2020

SKAFFOLD FLOW (MX) 5CC. Product Number: SKMX-FL05, UDI: 813845020894 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset with Filter, REF: A120-160XSFE

CME America, LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset with Filter and Manual Priming Valve, REF: A120-112XSFV

CME America, LLC

FDA Devices Moderate Jul 22, 2020

CRANIOSCULPT FLOW, CAN, 10CC, Product Number: C-FLOW10CC-CAN, UDI: 813845020375 - Product Usage: Callos is indicated to fill bony voids or gaps of t…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

OSTEOVATION IMPACT 10CC and OSTEOVATION, 10CC, IMPACT FORMULA, Product Number: 390-2110, UDI: 813845020092 - Product Usage: Callos is indicated to f…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended for use on the LIAISON MDX instrument for the qualitative detection of varicella-zoster…

DiaSorin Molecular LLC

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-161XPSV

CME America, LLC

FDA Devices Moderate Jul 22, 2020

Trinias DAP Meter, a component of the Digital Anglo System Trinias contained within the DAR-9500f - Product Usage: It is intended to be used for inte…

Shimadzu Medical Systems

FDA Devices Moderate Jul 22, 2020

OSTEOVATION RMX 5CC. Product Number: 390-6001, UDI: 813845021082 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal sys…

Skeletal Kinetics, Llc

FDA Devices Moderate Jul 22, 2020

ACUMED CALLOS INJECT 10CC. Product Number: 65-0010-S, UDI: 813845020245 - Product Usage: Callos is indicated to fill bony voids or gaps of the skele…

Skeletal Kinetics, Llc

FDA Devices Critical Jul 22, 2020

BodyGuard Microset, REF: A120-161XYBS

CME America, LLC

FDA Devices Moderate Jul 22, 2020

ACUMED CALLOS INJECT 3CC. Product Number: 65-0003-S, UDI: 813845020221 - Product Usage: Callos is indicated to fill bony voids or gaps of the skele…

Skeletal Kinetics, Llc

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

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