PlainRecalls

2020 Recalls

5,998 recalls · Page 59 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 7 critical, 41 moderate, and 2 lower-severity recalls. The page references 33 distinct recalling firms operating in 6 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (25), FDA Food (8), FDA Drug (7), 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 Jun 24, 2020

Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x40 mm Catalog Number: 18965040S - Product Usage: Stryker implants are single use devices intended …

Stryker GmbH

FDA Devices Moderate Jun 24, 2020

Mueller Knife Handle, Hexagonal - Product Usage: Intended to hold surgical blades.

Carefusion 2200 Inc

FDA Devices Moderate Jun 24, 2020

MAMMOMAT Revelation, model no. 11343300 - Product Usage: is intended to be used for mammography exams, screening, diagnostics, biopsies and dual ener…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jun 24, 2020

Stryker Locking Screw, Partially Threaded T2 Tibia ¿5x55 mm Catalog Number: 18915055S - Product Usage: Stryker implants are single use devices inten…

Stryker GmbH

FDA Devices Moderate Jun 24, 2020

Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and warmer.

GE Healthcare, LLC

FDA Devices Moderate Jun 24, 2020

BioFlo Midline Catheter and BioFlo Maximal Barrier Kits - Product Usage: These introducers are used for the percutaneous introduction of diagnostic o…

Angiodynamics, Inc.

FDA Devices Moderate Jun 24, 2020

Stryker 1 End Cap T2 Humerus ¿6mm, 5mm height Catalog Number: 18300005S - Product Usage: Stryker implants are single use devices intended for the …

Stryker GmbH

FDA Devices Moderate Jun 24, 2020

Biomet Outer Sheath 4.5/5.0,6.5- Orthopedic Manual Surgical Instrument Product Code: 14235

Biomet

FDA Devices Moderate Jun 24, 2020

PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: The Biosense Webster PENTARAY NAV High-Density Ma…

BIOSENSE WEBSTER

FDA Devices Moderate Jun 24, 2020

DDU-2400EN Lifeline PRO, UDI 00815098020270 - Product Usage: Automated External Defibrillators (AED) are indicated for use on victims of sudden cardi…

Defibtech, LLC

FDA Devices Moderate Jun 24, 2020

Xience Sierra TM Everolimus Eluting Coronary Stent System, RX 3.5mm x 33mmStrength: 100 ¿g/cm¿, Nominal Everolimus Content: 209 ¿g; Lot number 903224…

Abbott Vascular

FDA Devices Moderate Jun 24, 2020

Stryker End Cap T2 Humerus ¿6mm, 15mm height Catalog Number: 18300015S - Product Usage: Stryker implants are single use devices intended for the t…

Stryker GmbH

FDA Devices Moderate Jun 24, 2020

Leica ARveo and M530 OH6 microscope systems.

Leica Microsystems, Inc.

FDA Devices Moderate Jun 24, 2020

Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x30 mm Catalog Number: 18965030S - Product Usage: Stryker implants are single use devices intende…

Stryker GmbH

FDA Devices Moderate Jun 24, 2020

VITROS Chemistry Product AMYL Slides Reagent, AMYLASE/5 PACK/300 SLDS, Product Code 1202670, UDI # 10758750008513 - Product Usage: For in vitro dia…

Ortho-Clinical Diagnostics

FDA Devices Moderate Jun 24, 2020

Regard SRHS GIC Port A Cath, Sterile, Qty 20/case - Product Usage: The Saline Flush Syringes are intended to be used only for the flushing of indwell…

Resource Optimization & Innovation LLC

FDA Devices Moderate Jun 24, 2020

VITROS Chemistry Product Performance Verifier II, Product Code 8067324, UDI # 10758750004317 - Product Usage: For in vitro diagnostic use only to qua…

Ortho-Clinical Diagnostics

FDA Devices Moderate Jun 24, 2020

PENTARAY NAV eco HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: The Biosense Webster PENTARAY NAV High-Densit…

BIOSENSE WEBSTER

FDA Devices Moderate Jun 24, 2020

Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x50 mm Catalog Number: 18965050S - Product Usage: Stryker implants are single use devices intended …

Stryker GmbH

FDA Devices Moderate Jun 24, 2020

VITROS Chemistry Product AMYL Slides Reagent, AMYLASE/5 PACK/90 SLDS, Product Code 8112724, UDI # 10758750004393 - Product Usage: For in vitro diagno…

Ortho-Clinical Diagnostics

FDA Devices Moderate Jun 24, 2020

Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x35 mm Catalog Number: 18965035S - Product Usage: Stryker implants are single use devices intended …

Stryker GmbH

FDA Devices Moderate Jun 24, 2020

Stryker Locking Screw, Fully Threaded S2 05x35 mm Catalog Number: 17965035S - Product Usage: Stryker implants are single use devices intended for th…

Stryker GmbH

FDA Devices Moderate Jun 24, 2020

Alinity C, Processing Module. Chemistry analyzer for in-vitro diagnostics.

Abbott Gmbh & Co. KG

FDA Devices Moderate Jun 24, 2020

Stryker End Cap, Standard T2 Humerus ¿6 mm Catalog Number: 18300003S - Product Usage: Stryker implants are single use devices intended for the tem…

Stryker GmbH

FDA Devices Moderate Jun 24, 2020

Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x45 mm Catalog Number: 18965045S - Product Usage: Stryker implants are single use devices intended …

Stryker GmbH

CPSC Moderate Jun 24, 2020

The Furniture Connexion Recalls Modavari Forrest Live Edge Benches Due to Fall and Injury Hazards

Fred Meyer & Smith's Marketplace, of Portland, Ore.

NHTSA Critical Jun 24, 2020

TOYOTA 2019-2020: STEERING:ELECTRIC POWER ASSIST SYSTEM

TOYOTA

NHTSA Critical Jun 24, 2020

VOLKSWAGEN 2018: EQUIPMENT:OTHER:LABELS

VOLKSWAGEN

NHTSA Critical Jun 24, 2020

TOYOTA 2013-2017: HYBRID PROPULSION SYSTEM: INVERTER

TOYOTA

NHTSA Critical Jun 23, 2020

FORD,LINCOLN 2020: SEATS:MID/REAR ASSEMBLY

FORD,LINCOLN

NHTSA Critical Jun 23, 2020

FORD 2020: POWER TRAIN:AUTOMATIC TRANSMISSION:TORQUE CONVERTER

FORD

NHTSA Critical Jun 22, 2020

MERCEDES-BENZ 2020: ENGINE AND ENGINE COOLING:ENGINE:GASOLINE:TURBO/SUPERCHARGER

MERCEDES-BENZ

CPSC Moderate Jun 18, 2020

Lochinvar Recalls Condensing Residential Boilers Due to Risk of Carbon Monoxide Poisoning

Lochinvar LLC, of Lebanon, Tenn.

CPSC Moderate Jun 18, 2020

Modus Furniture Recalls Dressers Due to Tip-Over and Entrapment Hazards: In-Home Remedy May be Delayed Due to COVID-19 Restrictions; Keep Product Awa…

CPSC Moderate Jun 18, 2020

Recreational Off-Highway Vehicles Recalled by American Honda Due to Crash and Injury Hazards (Recall Alert)

American Honda Motor Co., Inc., of Torrance, Calif.

FDA Food Moderate Jun 17, 2020

La Sonorense Tortilla Factory, Flour Burrito Size, One Dozen, NET WT. 1 lb. 6 oz. (22 oz.)

La Sonorense, Inc.

FDA Food Moderate Jun 17, 2020

La Sonorense Tortilla Factory, Gorditas Sonora Style, One Dozen, NET WT. 1 lb. 6 oz. (22 oz.)

La Sonorense, Inc.

FDA Food Moderate Jun 17, 2020

085-CH-550-35 Cheese Whiz-Small Bag, 085-CH-550-35: 35 lbs. Multiwall bags .

World Flavors, Inc.

FDA Food Moderate Jun 17, 2020

Adams Reserve Sweet & Spicy Seafood Salmon NEY WT 2.5 OZ (73g) UPC code 4313 04950.

Adams Extract & Spice LLC

FDA Food Moderate Jun 17, 2020

Healthy Choice Pesto and Egg bowls labeled in the following ways: 1) (for the US market) Healthy Choice Power Bowls Morning Pesto & Egg White Scrambl…

ConAgra Foods, INc.

FDA Food Moderate Jun 17, 2020

Wild Harvest Organic Fresh Basil packaged in the following sized plastic containers: Net Wt 2 oz (57g), UPC 11535-50762, Net Wt 0.25 oz. (7g), U…

UNFI General Corporate

FDA Food Moderate Jun 17, 2020

Bin Butternut Squash, Bulk, Raw Product in Bins / 4, 5lb packages in each case

Coastal Sunbelt Produce Co. Inc.

FDA Food Moderate Jun 17, 2020

025-BBQ-468 Barbeque Sauce Base, 50 lbs. Multiwall bags .

World Flavors, Inc.

FDA Drug Critical Jun 17, 2020

Ketorolac Tromethamine Injection, USP, 30 mg per mL, packaged in 1 mL Single Dose Vials (NDC 63323-162-00); 25 x 1 mL Single Dose Vials per tray (NDC…

Fresenius Kabi USA, LLC

FDA Drug Low Jun 17, 2020

Prednisolone Sodium Phosphate Oral Solution, 5 mg/5 mL, 120 mL Bottle, Rx only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC: 50383-040-04

Akorn, Inc.

FDA Drug Low Jun 17, 2020

Clonidine Hydrochloride Tablets, USP 0.1 mg 100-count bottles, Rx only, Manufactured by: Unichem Laboratories LTD. Pilerne Ind. Estate, Pilerne, Bard…

UNICHEM PHARMACEUTICALS USA INC

FDA Drug Moderate Jun 17, 2020

oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only, QuVa Pharma 1075 West Park One Drive, Suite 100…

QuVa Pharma, Inc.

FDA Drug Moderate Jun 17, 2020

Lisinopril Tablets, USP, 5 mg, Rx Only, 1000-count bottle, Manufactured for: Lupin Pharmaceuticals Inc., Baltimore, MD 21202, Manufactured by: Lupin …

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Jun 17, 2020

Ketorolac Tromethamine Injection, USP, 60 mg per 2 mL (30 mg per mL), packaged in 2 mL Single Dose Vials (NDC 63323-162-03), 25 x 2 mL Single Dose Vi…

Fresenius Kabi USA, LLC

FDA Drug Moderate Jun 17, 2020

Unasyn (ampicillin sodium/sulbacatam) for injection, 1.5 g* per vial, Rx Only, 10 vials/carton, Made in Italy Distributed by Roerig Division of Pfize…

Pfizer 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

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.