PlainRecalls

2020 Recalls

4,819 recalls · Page 52 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 9 critical, 40 moderate, and 1 lower-severity recalls. The page references 33 distinct recalling firms operating in 6 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (22), NHTSA (8), FDA Food (8), 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 10, 2020

Sterile Custom Packs to be used in surgical procedures.

American Contract Systems

CPSC Moderate Jun 10, 2020

DICK'S Sporting Goods Recalls Safety Ropes Due to Fall and Injury Hazards

DICK'S Sporting Goods, of Coraopolis, Pa.

CPSC Moderate Jun 10, 2020

Island Wear Recalls Strollers Due to Violation of Federal Stroller and Carriage Safety Standard; Fall and Choking Hazards

CPSC Moderate Jun 10, 2020

Ushio America Recalls Indiglow LED T8 Lamps Due to Injury Hazard

NHTSA Critical Jun 9, 2020

MERCEDES-BENZ 2019: POWER TRAIN:DRIVELINE:DRIVESHAFT

MERCEDES-BENZ

NHTSA Critical Jun 8, 2020

FORD 2014-2017: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER

FORD

NHTSA Moderate Jun 8, 2020

FORD,LINCOLN 2011-2016: LATCHES/LOCKS/LINKAGES:DOORS:LATCH

FORD,LINCOLN

NHTSA Critical Jun 5, 2020

MERCEDES-BENZ 2020: SUSPENSION:REAR:SHOCK ABSORBER

MERCEDES-BENZ

NHTSA Critical Jun 5, 2020

MERCEDES-BENZ 2020: SEATS:MID/REAR ASSEMBLY

MERCEDES-BENZ

CPSC Moderate Jun 4, 2020

Capstone Holdings Recalls Simply Earth Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Rec…

Capstone Holdings LLC, dba Simply Earth, of Waldo, Wis.

CPSC Moderate Jun 4, 2020

Tim Trading Recalls Emori Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

Emori, of Rowland Heights, Calif.

NHTSA Critical Jun 4, 2020

HONDA 2019: SEAT BELTS:REAR/OTHER

HONDA

NHTSA Critical Jun 4, 2020

LAND ROVER 2016: LATCHES/LOCKS/LINKAGES:DOORS:LATCH

LAND ROVER

NHTSA Critical Jun 4, 2020

CHEVROLET,GMC 2020: STRUCTURE:BODY:HOOD

CHEVROLET,GMC

FDA Food Critical Jun 3, 2020

RITZ Cheese Cracker Sandwiches , Family Size , (21.6 oz. carton)

Mondelez Global Llc

FDA Food Moderate Jun 3, 2020

Milkadamia Salted Buttery Spread 8 ounces packaged in plastic tub, 6 packaged per case UPC 858045004718

Jindilli Beverages LLC

FDA Food Moderate Jun 3, 2020

Home Style Crab Cakes in a plastic wrapped foam tray, 12 oz. (Four, 3 oz. crab cakes per package). 12 packages per case.

Johnson Sea Products, Inc.

FDA Food Moderate Jun 3, 2020

Wegmans Tuna Salad, 16 OZ (1 LB) 454 g; UPC: 77890-48147; SELL BY 5/21/20

Wegmans Food Markets, Inc.

FDA Food Moderate Jun 3, 2020

Milkadamia Unsalted Buttery Spread 8 ounces packaged in plastic tub, 6 packaged per case UPC 858045004725

Jindilli Beverages LLC

FDA Food Moderate Jun 3, 2020

Wegmans Tuna Salad on Roasted Tomato Pita, 9 oz.; UPC: 2-27390-00000; SELL BY 5/14-5/16

Wegmans Food Markets, Inc.

FDA Food Moderate Jun 3, 2020

Siete Grain Free Cashew Flour Tortillas NET WT 7 OZ (200g) 8 Count UPC 865336000045 packaged in flexible plastic

GARZA FOOD VENTURES

FDA Food Moderate Jun 3, 2020

Absorb Health Advanced Joint Relief Joint Health; 510mg; 90 CAPSULES; Manufactured for: Absorb Health, 106 Countryside St NW, Supply, NC 28462 UPC 79…

Absorb Health LLC

FDA Drug Moderate Jun 3, 2020

Doxycycline Hyclate Tablets USP, 100 mg, packaged in a) 50-count bottle (NDC 0143-2112-50), b) 500-count bottle (NDC 0143-2112-05), Rx only, Mfd. by:…

West-Ward Columbus Inc

FDA Drug Moderate Jun 3, 2020

LidoPro (lidocaine 4%, menthol 5%, methyl salicylate 4%) patch, 15 Patches per box, Manufactured For: Terrain Pharmaceuticals, Reno, NV 89501; NDC 53…

Wuhan Bingbing Pharmaceutical Co., Ltd.

FDA Drug Moderate Jun 3, 2020

Mencaine (lidocaine 4.5%, menthol 5%) Patch, 1 patch per pouch, Manufactured For: Terrain Pharmaceuticals, Reno, NV 89501; NDC 53225-1090-1.

Wuhan Bingbing Pharmaceutical Co., Ltd.

FDA Drug Moderate Jun 3, 2020

Maximum Strength Lidocaine Cold & Hot Patch (lidocaine 4%, menthol 1%), 5 patches per box, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsoc…

Wuhan Bingbing Pharmaceutical Co., Ltd.

FDA Drug Moderate Jun 3, 2020

Doxycycline Hyclate tablets USP, 100 mg, packaged in bottles a) 6-count (NDC 55289-866-06), b) 10-count (NDC 55289-866-10), c) 14-count (NDC 55289-86…

PD-Rx Pharmaceuticals, Inc.

FDA Drug Moderate Jun 3, 2020

LidoPatch (lidocaine HCl 3.6%, menthol 1.25%) Pain Relief Patch, packaged in 1 patch/box (NDC 10882-527-01); 30 patches/box (NDC 10882-527-02 and 108…

Wuhan Bingbing Pharmaceutical Co., Ltd.

FDA Drug Low Jun 3, 2020

Lamotrigine Tablets, USP, 150 mg, 20,000-count bulk container, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA, For …

Jubilant Cadista Pharmaceuticals, Inc.

FDA Devices Moderate Jun 3, 2020

Samco Bio-Tite Sterile Specimen Container, 120mL/53mm, Bio-Tite Blue Cap Catalog Number: 07 0006 The specimen containers are used for temporary …

Thermo Fisher Scientific (Monterrey)

FDA Devices Moderate Jun 3, 2020

Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD

Cardinal Health Inc.

FDA Devices Moderate Jun 3, 2020

Thirty-five (35) cm 8 Contact Extension Kit, part number M365SC3138350. Package Contents: Lead Extension Kit (1) Lead Extension (1) Hex Wrench (…

Boston Scientific Neuromodulation Corporation

FDA Devices Moderate Jun 3, 2020

Ref 801168, MPS Top Cover Replacement Kit, 1 UNITS, UDI: (01)2 0634624 81168 7 (11)190916 (17)290913 (10)059135 (The device is a component of the M…

Quest Medical, Inc.

FDA Devices Moderate Jun 3, 2020

DR. THAMES - LAP CHOLE, REF: K0880, UDI: (01)30607915139620

Applied Medical Resources Corp

FDA Devices Critical Jun 3, 2020

Heartware HVAD Pump Implant Kit, Product (REF) Number 1103

Heartware, Inc.

FDA Devices Moderate Jun 3, 2020

LinearTM 3-4 50 cm 8 Contact Lead Kit, part number M365SC2352500. Leads function as a component of Boston Scientific's Spinal Cord Stimulation (SCS…

Boston Scientific Neuromodulation Corporation

FDA Devices Moderate Jun 3, 2020

Kangaroo 924 Safety Screw Spike Set, Product Code 775759

Cardinal Health Inc.

FDA Devices Moderate Jun 3, 2020

Fifty-five (55) cm 8 Contact Extension Kit, part number M365NM3138550 - Product Usage: The Deep Brain Stimulation (DBS) System is indicated for use …

Boston Scientific Neuromodulation Corporation

FDA Devices Moderate Jun 3, 2020

Knee Products: 154335 Oxford Partial Knee System, Fixed Lateral Tibial Construct, Left, Cemented, D3 154336 Oxford Partial Knee System, Fixed Later…

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

ABL90 FLEX, model no. 393-090; and Spare Part Hemolyzer Units (902-980): R0526 - R0941 - Product Usage: are intended for use by trained technologist…

Radiometer Medical ApS

FDA Devices Moderate Jun 3, 2020

VACUETTE Blood Transfer Unit. Lot no. A19024NX. Expiration date: 2022-02-07 - Product Usage: The Blood Transfer Unit is used to transfer blood from a…

C.A. Greiner & Sohne Gesellschaftmbh

FDA Devices Moderate Jun 3, 2020

Knee Products: 184762 Knees Vanguard Knee System, Series-A Standard Patella, 28 MM; 184764 Knees Vanguard Knee System, Series-A Standard Patella,…

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

ISE Electrolyte Reference (2 X 2L) Reagent, REF A28937, UDI: 15099590202491 - Product Usage: are intended for the quantitative determination of carbo…

Beckman Coulter Inc.

FDA Devices Moderate Jun 3, 2020

Clip Applier Kit, REF: K2887, UDI: (01)30607915139132(17)220822(30)1(10)

Applied Medical Resources Corp

FDA Devices Moderate Jun 3, 2020

Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01,…

Inpeco S.A.

FDA Devices Moderate Jun 3, 2020

Bridge Occlusion Balloon, REF 590-001, QTY 1, Sheath Compatibility 12F, Guidewire Compatibility 0.035 in, Working Length 90 cm, Balloon Outer Diamete…

Spectranetics Corporation

FDA Devices Moderate Jun 3, 2020

Body Weight Support (BWS) Light; Model No. RB011; a component of C-Mill, Grail, M-Gait - Product Usage: is designed to facilitate functional gait tra…

MOTEK MEDICAL B.V.

FDA Devices Moderate Jun 3, 2020

Knee Products: TMJPM-1510 Microfixation Custom Made Device, Left PM-TMJ Model (01)00841036226534(17)220111(10)735550 Product Usage: Knee prosthe…

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

Knee Products: 189260 Vanguard Knee System, CR-L Mono Lock Tibial Bearing, 10 MM X 71 MM 189720 Vanguard Knee System, CR Mono Lock Tibial Bearing, …

Biomet, Inc.

FDA Devices Moderate Jun 3, 2020

Knee Products: US154709 Knees Vanguard M Partial Knee System MonoBlock Tibial Tray, Right Medial/Left Lateral, B8 US154722 Knees Vanguard M Partial…

Biomet, 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