PlainRecalls

2020 Recalls

4,819 recalls · Page 43 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 15 critical, 29 moderate, and 6 lower-severity recalls. The page references 27 distinct recalling firms operating in 7 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (30), FDA Drug (7), CPSC (6), 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 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.

CPSC Moderate Jul 22, 2020

BioMed Balance Recalls Wintergreen and Sweet Birch Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning

BioMed Balance, of Kent, Wash.

CPSC Moderate Jul 22, 2020

Cookware Company Recalls Greenpan SimmerLite Dutch Ovens Due to Burn and Injury Hazards

CPSC Moderate Jul 22, 2020

DownEast Outfitters Recalls Folding Mattresses Due to Violation of Federal Mattress Flammability Standard

Relux Mattress Co. Ltd., of China

CPSC Moderate Jul 22, 2020

Manhattan Toy Recalls 'Manhattan Ball' Activity Toys Due to Choking Hazard; Sold Exclusively at Target

NHTSA Critical Jul 22, 2020

KIA 2020: STEERING

KIA

NHTSA Critical Jul 17, 2020

FORD 2020: AIR BAGS:SIDE/WINDOW

FORD

NHTSA Critical Jul 17, 2020

LINCOLN 2016-2020: SEATS:FRONT ASSEMBLY:POWER ADJUST

LINCOLN

NHTSA Moderate Jul 17, 2020

FORD 2021: STRUCTURE:FRAME AND MEMBERS:UNDERBODY SHIELDS

FORD

NHTSA Critical Jul 17, 2020

NISSAN 2020: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

NISSAN

CPSC Moderate Jul 16, 2020

Polaris Recalls Snowmobiles Due to Fire Hazard (Recall Alert)

Polaris Industries Inc., Medina, Minn.

CPSC Moderate Jul 16, 2020

Rocky Mountain Bicycles Recalls Non-Electric Instinct, Instinct BC and Pipeline Bicycles with Alloy Frames Due to Fall and Injury Hazards

Rocky Mountain Bicycles, of Canada

FDA Food Critical Jul 15, 2020

Fresh Express Chopped Kit SOUTHWEST TOTAL NET WT. 11.5 oz (326g) plastic bag. FRESH EXPRESS INCORPORATED P.O. BOX 80599, SALINAS, CA 93912 UPC 0 712…

Fresh Express Incorpated

FDA Food Moderate Jul 15, 2020

Blanxart 85% Nicaragua Organic Dark Chocolate Bar, packaged in paper packaging with internal foil wrapper. Net weight 4.4 oz (125 g). UPC 8 32924 000…

Power Selles Imports dba Culinary Collective

FDA Drug Low Jul 15, 2020

Brimonidine Tartrate Opthalmic Solution 0.2%, 10 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Made in India.…

SOMERSET THERAPEUTICS LLC

FDA Drug Low Jul 15, 2020

Tecfidera (dimethyl fumarate) delayed-release capsules, 240 mg, 60-count bottle, Rx only, Manufactured by: Biogen Inc., Cambridge, MA 02142, NDC 6440…

Biogen MA Inc.

FDA Drug Low Jul 15, 2020

Brimonidine Tartrate Opthalmic Solution 0.2%, 15 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Made in India.…

SOMERSET THERAPEUTICS LLC

FDA Drug Low Jul 15, 2020

Nystatin Oral Suspension, USP 500,000 units/5mL Cup, Delivers 5 mL, Rx Only, Manufactured by: VistaPharm, Largo, FL 33771, a) NDC 66689-037-50 (indi…

VistaPharm, Inc.

FDA Drug Low Jul 15, 2020

Nystatin Oral Suspension, USP 100,000 units per mL, Bubblegum Flavored, 16 fl. oz. bottle (480 mL), Shake Well Before Using, Rx Only, Manufactured by…

VistaPharm, Inc.

FDA Drug Low Jul 15, 2020

Brimonidine Tartrate Opthalmic Solution 0.2%, 5 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Made in India. …

SOMERSET THERAPEUTICS LLC

FDA Drug Moderate Jul 15, 2020

Cetrotide (cetrorelix acetate for Injection) 0.25 mg, Sterile - for subcutaneous use only, Rx Only, Manufactured for: EMD Serono, Inc., Rockland, MD …

EMD Serono, Inc.

FDA Devices Moderate Jul 15, 2020

3COR DISTRACTION SCREW, 12 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.

TeDan Surgical Innovations LLC

FDA Devices Moderate Jul 15, 2020

CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H7mm, Part #018.1907.

CTL Medical Corporation

FDA Devices Moderate Jul 15, 2020

OrthoPediatrics ACL Reconstruction System ShieldLoc 7mm implant component model number 10-1008-4070 - Product Usage: is intended for fixation of tend…

OrthoPediatrics Corp

FDA Devices Moderate Jul 15, 2020

Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH PE 85 cm x 4.0 mm 58124 40US

Prodimed Plastimed Division

FDA Devices Moderate Jul 15, 2020

TOMTEC-ARENA TTA2;software version no. 2.20 and lower; Picture archiving and communications system. Software Versions and applicable UDI: TTA 1…

Tomtec Imaging Systems Gmbh

FDA Devices Moderate Jul 15, 2020

PHANTOM CS DISTRACTION SCREW, 12 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical sp…

TeDan Surgical Innovations LLC

FDA Devices Moderate Jul 15, 2020

Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes. Sterile and single use only. Catalog number ENF-80P-50 (8 fr. 50 cm ENFit En…

Kentec Medical, Inc

FDA Devices Moderate Jul 15, 2020

Blood gases (PCO2, PO2) and blood pH test system; ABL800 FLEX; Model Number 393-800; UDI (01)05700693938004. Model 393-800 is available in the follow…

Radiometer Medical ApS

FDA Devices Moderate Jul 15, 2020

Prodimed Combicath Paediatric catheters for blind protected distal bronchial sampling- COMBICATH 35 cm x 1.9 mm Product Code: 58 223 19US

Prodimed Plastimed Division

FDA Devices Moderate Jul 15, 2020

COOPERSURGICAL Os FinderTM Cervical Dilator, Taper: 2.0 mm to 4.0 mm OD Length: 21.5 cm Box of 50 Part Number: 1176

CooperSurgical, Inc.

FDA Devices Moderate Jul 15, 2020

Percepta CRT-P MRI, Model Numbers: a) W1TR01, b) W1TR04, c) W4TR01, d) W4TR04

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA Devices Moderate Jul 15, 2020

PHANTOM CS QUICK START DISTRACTION SCREW, 12 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the …

TeDan Surgical Innovations LLC

FDA Devices Moderate Jul 15, 2020

Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH PE 60 cm x 2.7 mm Product Code: 58216 27US

Prodimed Plastimed Division

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