PlainRecalls

2020 Recalls

5,998 recalls · Page 51 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 12 critical, 36 moderate, and 2 lower-severity recalls. The page references 13 distinct recalling firms operating in 4 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (37), FDA Drug (10), FDA Food (3), 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 Food Moderate Jul 22, 2020

Giant Eagle Chopped BBQ Ranch Salad Kit 11.3 oz., UPC 030034923303, Cabbage and lettuce, carrots, and green onion

Fresh Express Incorporated

FDA Food Moderate Jul 22, 2020

Little Salad Bar Sunflower Chopped Salad Kit 11.1 oz., UPC 4099100087901, Green and red cabbage, green leaf lettuce & carrots

Fresh Express Incorporated

FDA Food Moderate Jul 22, 2020

Hy-Vee Chopped Kit Avocado Ranch Salad 12.8 oz., UPC 075450247152, Green cabbage, romaine lettuce, carrots, cilantro & green onions

Fresh Express Incorporated

FDA Drug Moderate Jul 22, 2020

Lidothol Patch, Lidocaine 4.5% & Menthol 5%, In each patch: lidocaine 4.5% topical anesthetic, menthol 5% topical analgesic, Pkg Size 15 patches per …

Preferred Pharmaceuticals, Inc.

FDA Drug Moderate Jul 22, 2020

Metformin Hydrochloride Extended-release Tablets USP 500 mg, 100 count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Manufactured …

Lupin Pharmaceuticals Inc.

FDA Drug Low Jul 22, 2020

Fosaprepitant for Injection, 150 mg / vial in a 10 mL Single-Dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047; NDC 63323-972-10

Fresenius Kabi USA, LLC

FDA Drug Moderate Jul 22, 2020

Metformin Hydrochloride Extended-Release Tablets USP, 750 mg, a) 100 ct. bottle (NDC 70010-492-01) and 500 ct. bottle (NDC 70010-492-05), Manufacture…

Granules Pharmaceuticals Inc

FDA Drug Low Jul 22, 2020

Proparacaine Hydrochloride Ophthalmic Solution, USP, 0.5%, 15 mL per dropper bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL …

Akorn, Inc.

FDA Drug Moderate Jul 22, 2020

Metformin Hydrochloride Extended-Release Tablets USP 1000 mg, 60 count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Manufactured …

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Jul 22, 2020

Metformin Hydrochloride Extended-Release Tablets USP 500 mg, 60 count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Manufactured b…

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Jul 22, 2020

Auryxia (ferric citrate) tablets 210 mg, Rx Only, 200 tablets per bottle, Manufactured for and distributed by: Keryx Biopharmaceuticals, Inc., 245 Fi…

Keryx Biopharmaceuticals, Inc.

FDA Drug Moderate Jul 22, 2020

Metformin Hydrochloride Extended-Release Tablets USP 1000 mg, 90 count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Manufactured …

Lupin Pharmaceuticals Inc.

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

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.