PlainRecalls

2020 Recalls

4,819 recalls · Page 53 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 14 critical, 34 moderate, and 2 lower-severity recalls. The page references 33 distinct recalling firms operating in 4 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (32), FDA Food (10), NHTSA (5), 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 Moderate Jun 3, 2020

Epix latis GRASPER, 5 mm x 35 cm, REF C4130, Qty: 10, Sterile R, CE, Rx ONLY, UDI: (01)00607915110147

Applied Medical Resources Corp

FDA Devices Moderate Jun 3, 2020

Knee Products: 150414 Orthopedic Salvage System (OSS) Tibial Bearing, 20 MM Standard - Product Usage: Knee prosthesis

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

Nikon Metrology XTH cabinet x-ray Systems which includes variations STH225, XTH225ST, and MCT225.

Nikon Metrology

FDA Devices Moderate Jun 3, 2020

Knee Products: 155308 Knees AGC Knee System PS Molded Tibial Component, 10 MM X 65 MM 155326 Knees AGC Knee System PS Molded Tibial Component, 10 M…

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jun 3, 2020

Kangaroo Epump Safety Screw Spike with Flush Bag, Anti-free Flow, 1000 mL, Product Code 775100

Cardinal Health Inc.

FDA Devices Critical Jun 3, 2020

Heartware HVAD Pump Outflow Graft, Product (REF) Number 1125

Heartware, Inc.

FDA Devices Moderate Jun 3, 2020

JOURNEY II UNI RESECTION PREP TRIAL, LEFT MEDIAL/ RIGHT LATERAL - Product Usage: The JOURNEY II Uni Resection Prep Trial is a reusable surgical instr…

Smith & Nephew, Inc.

FDA Devices Moderate Jun 3, 2020

da Vinci SP Camera; PN 430060-33; Model Number: 430060-33. For endoscopic surgery.

Intuitive Surgical, Inc.

FDA Devices Moderate Jun 3, 2020

Extremities Item Number: 1)113954 Hybrid Glenoid Glenoid Base, 4 MM 2) XL-115366 Comprehensive Reverse Shoulder Humeral Bearing, ArComXL, 44 MM X…

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

Knee Products: 183622 Vanguard Knee System PS Tibial Bearing, 12 MM X 63/67 MM 183620 Vanguard Knee System PS Tibial Bearing, 10 MM X 63/67 MM 189…

Biomet, Inc.

FDA Devices Critical Jun 3, 2020

Heartware HVAD Pump Implant Kit, Product (REF) Number 1104

Heartware, Inc.

FDA Devices Moderate Jun 3, 2020

Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product Usage: is for use in the hospital by qualified medical personnel trained…

Philips North America, LLC

FDA Devices Moderate Jun 3, 2020

Epix latis GRASPER, 5mm x 45 cm, REF: C4140, Qty: 10, Sterile R, CE, Rx ONLY, UDI: (01)00607915110154

Applied Medical Resources Corp

FDA Devices Moderate Jun 3, 2020

Clearview Total Uterine Manipulator (model UM750), The device is labeled in part, "ClearView(R) TOTAL, 7 cm* * *CLINICAL INNOVATIONS Manufacturer: C…

Clinical Innovations, LLC

FDA Devices Moderate Jun 3, 2020

CooperSurgical Dilator/Sound Set, Rx only, Sterile/EO, Made in South Korea, P/N MX21

CooperSurgical, Inc.

FDA Devices Moderate Jun 3, 2020

Panther Fusion Extraction Reagent-S, Ref PRD-04331, IVD, CE, Rx Only consisting of FCR-S Fusion Capture Reagent - S, Nucleic Acid in a buffered solut…

Hologic, Inc

FDA Devices Moderate Jun 3, 2020

Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are an accessory to the compatible monitor/defibrillator Switchless: M1741A…

Philips North America, LLC

FDA Devices Critical Jun 3, 2020

Medtronic Confida Expandable Sheath, REF CES122230. To provide a guide for catheters or devices introduced into the femoral iliac arteries.

Medtronic Vascular Galway DBA Medtronic Ireland

FDA Devices Moderate Jun 3, 2020

Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.

GE Healthcare, LLC

FDA Devices Moderate Jun 3, 2020

FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-1…

Inpeco S.A.

FDA Devices Moderate Jun 3, 2020

Knee Products: 189420 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM 189422 Vanguard Knee System, PS Mono Lock Tibial Bearing, 12…

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

Fifty-five (55) cm 8 Contact Extension Kit, part number M365SC3138550 - Product Usage: Lead Extensions are designed to connect the percutaneous lea…

Boston Scientific Neuromodulation Corporation

FDA Devices Critical Jun 3, 2020

Heartware HVAD Pump Implant Kit, Product (REF) Number 1104JP

Heartware, Inc.

FDA Devices Moderate Jun 3, 2020

Hip Products Item Number: 1) 110010462 RingLoc Hip System, Acetabular Bi-Polar Cup, 28 MM X 51 MM 2) 11-165218 RingLoc Bi-Polar Hip System, Aceta…

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

Knee Products: 141356 Regenerex Series-A Patella 3 Peg, 31 MM 141358 Regenerex Series-A Patella 3 Peg, 37 MM Product Usage: Knee prosthesis

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

JOURNEY II UNI RESECTION PREP TRIAL, RIGHT MEDIAL/ LEFT LATERAL - Product Usage: The JOURNEY II Uni Resection Prep Trial is a reusable surgical instr…

Smith & Nephew, Inc.

FDA Devices Moderate Jun 3, 2020

Skater Introducer Set 6F x 18cm. REF/UDI: 651506300/(01)00886333005000; 655506300/(01)00886333005079 - Product Usage: The Skater Introducer System wi…

Argon Medical Devices, Inc

FDA Devices Moderate Jun 3, 2020

Precision TM M8 Adapter, 15 cm, part number M365SC9218150 - Product Usage: The adapter is part of a spinal cord stimulation system for prescription u…

Boston Scientific Neuromodulation Corporation

FDA Devices Moderate Jun 3, 2020

ABL90 FLEX PLUS, model no. 393-02; and Spare Part Hemolyzer Units (902-980): R0526 - R0941 - Product Usage: are intended for use by trained technolog…

Radiometer Medical ApS

FDA Devices Moderate Jun 3, 2020

Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A, M3536A, and M3536M - Product Usage: is for use for the termination of ventricul…

Philips North America, LLC

FDA Devices Moderate Jun 3, 2020

GENTLEWAVE REF: FG-002-0001

Sonendo Inc

NHTSA Critical Jun 3, 2020

MERCEDES-BENZ 2019-2020: AIR BAGS:SIDE/WINDOW

MERCEDES-BENZ

NHTSA Critical Jun 2, 2020

BENTLEY 2019: FUEL SYSTEM, GASOLINE:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS

BENTLEY

NHTSA Critical May 29, 2020

CHEVROLET 2019: ELECTRICAL SYSTEM:SOFTWARE

CHEVROLET

NHTSA Critical May 28, 2020

NISSAN 2013-2018: LATCHES/LOCKS/LINKAGES:HOOD:LATCH

NISSAN

NHTSA Critical May 28, 2020

ACURA,HONDA 2018-2020: FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP

ACURA,HONDA

FDA Food Moderate May 27, 2020

Willamette Valley Pie Company Raspberry Rhubarb Pie, packaged in clamshells container, six containers per case. Each pie weighs 10 oz. and sold as i…

Willamette Valley Pie Company, LLC.

FDA Food Moderate May 27, 2020

Lay's French Onion dip 15 oz. UPC 2840007094 packaged in clear glass jars

Frito-Lay, Inc.

FDA Food Critical May 27, 2020

Wegmans brand Semi-Sweet Chocolate Nonpareils in an 18.5 oz. (524 g) plastic container, 12 plastic containers per case.

Mellace Family Brands California Inc

FDA Food Moderate May 27, 2020

Willamette Valley Pie Company Cherry Pie, packaged in clamshells container, six containers per case. Each pie weighs 10 oz. and sold as individual p…

Willamette Valley Pie Company, LLC.

FDA Food Moderate May 27, 2020

Ruffles Ranch flavoured dip 425 g (15 oz). UPC 6041007299 packaged in clear glass jars

Frito-Lay, Inc.

FDA Food Critical May 27, 2020

43559 SNDW Chicken Sandwich on White Single, vacuumed pack bag, Clam shell. Label UPC: 50777444804, Condies Foods Inc. PO Box 18548. Salt Lake City…

Condies Foods, Inc.

FDA Food Moderate May 27, 2020

RICKER HILL ORCHARDS APPLE CIDER McIntosh Blend, 1 GAL (128 FL OZ) and 1/2 GAL (64 FL OZ); UPC: 0 74613 80009 8; MADE IN MAINE; KEEP REFRIGERATED; Pr…

Ricker Hill Farms, Inc.

FDA Food Critical May 27, 2020

43237 ROLL chicken salad on croissant single, vacuumed pack bag, Clam shell. Label UPC: 50777445351, Condies Foods Inc. PO Box 18548. Salt Lake Ci…

Condies Foods, Inc.

FDA Food Critical May 27, 2020

Peekaboo Ice Cream + hidden Veggies; Organic Mint Chocolate Chip with Hidden Spinach, 14 oz. carton: UPC: 868540000115 Manufactured for: Peekab…

Ramar International Corporation

FDA Food Moderate May 27, 2020

Ruffles Onion flavoured dip 425 g (15 oz). UPC 6041007298 packaged in clear glass jars

Frito-Lay, Inc.

FDA Drug Low May 27, 2020

Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC: 0054-0415-…

West-Ward Columbus Inc

FDA Drug Critical May 27, 2020

LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09

ICU Medical Inc

FDA Drug Low May 27, 2020

Gabapentin Tablets USP, 600 mg, Rx Only, 500-count bottle, Manufactured for: Exelan Pharmaceuticals, Inc., Lawrenceville, GA 30046, Manufactured by: …

InvaGen Pharmaceuticals, 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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2020