PlainRecalls

2020 Recall Year Insight

Federal agencies issued 6,048 product recalls indexed by PlainRecalls in calendar year 2020. That represents about 5.79% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 16.6 recalls per day across the FDA, CPSC, USDA FSIS, 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 121 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 8 critical, 41 moderate, and 1 lower-severity recalls. The page references 34 distinct recalling firms operating in 7 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (20), FDA Food (10), NHTSA (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, USDA FSIS, 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 10, 2020

Multifire VersaTrack Auto Suture Hernia Stapler, 4.8mm, Part No. 174023 - Product Usage: has application in endoscopic general surgery procedures for fixation of mesh in the repair of hernial defects and in other surgical specialties for approximation of tissue(s).

Covidien Llc

FDA Devices Moderate Jun 10, 2020

OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.

Osteomed, LLC

FDA Devices Moderate Jun 10, 2020

Power supply provided with Afinion 2, Catalog numbers 1116553, 1116554, 1116556, 1116557, 1116597, 1116598, 1116663, 1116679, 1116680, 1116681, 1116682, 1116684, 1116770, 1116771, 1116772, 1116777, 1116778, 1116970, 1116971, 1116985, 1116986, IVD. The firm name on the label is Abbott Diagnostics Technologies AS, Oslo, Norway. Power supply provided with Alere Afinion AS100 Analyzer, Catalog numbers 1115175, 1115390, 1116049, 1116050, 1116053, 1116054, 1116456, and 1116980. The firm name on t

Abbott Diagnostics Technologies AS

FDA Devices Moderate Jun 10, 2020

AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic, Type number: 6010/200 - Product Usage: DR 800: Agfa s DR 800 system is indicated for performing dynamic imaging examinations (fluoroscopy and/or rapid sequence) of the following anatomies/procedures: positioning fluoroscopy procedures, gastro-intestinal examinations, urogenital tract examinations, and angiography. It is intended to replace fluoroscopic images obtained through image intensifier technology. In addition, the system

Agfa N.V.

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants VITAL MIS TAB BREAKER, Item Number 850M0055 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is indicated for skeletally mature patients and for adolescence patients.

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 10, 2020

OSTEOVATIONEX 3CC IMPACTFORMULA. REF/UDI: 390-0203/00813845020030 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.

Osteomed, LLC

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X50MM, Item Number 811M8550 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is indicated for skeletally mature patients and for adolescence patients.

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 10, 2020

Cardiovascular Monitoring Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration bellows, or respiration sensor) monitors bellows-derived respiration by detecting abdominal or chest wall motion. The chest pneumograph is an accessory to a MRI patient monitoring system or MRI gating solution. The Chest Pneumograph is indicated for use by healthcare professionals with the Wireless Sp02 (wSp02) Module or Toshiba KSB gating unit when bellows-de

Philips North America, LLC

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 7.5X40MM, Item Number 810M7540 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is indicated for skeletally mature patients and for adolescence patients.

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 10, 2020

Accelerator APS Aliquoter Module, List number: 07L40 - Product Usage: The ACCELERATOR APS Workcell is a modular system designed to automate sample handling and processing in the clinical laboratory. The system allows consolidations of multiple clinical chemistry and immunoassay analytical instruments into a unified workstation.

Abbott Laboratories

FDA Devices Moderate Jun 10, 2020

Healing Abutment Conical Connection RP 0 3.6 x 5mm, REF: 36644, UDI: 07332747034462 - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to restore chewing function. The Healing Abutment is intended to be used as a temporary component to an endosseous implant to allow healing of the soft tissue.

Nobel Biocare Usa Llc

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X50MM, Item Number 810M6550 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is indicated for skeletally mature patients and for adolescence patients.

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 7.5X35MM, Item Number 810M7535 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is indicated for skeletally mature patients and for adolescence patients.

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 10, 2020

Omnipod DASH Insulin Management System (mmol/L configuration), Catalog Number PT000011 M/D: INT1D001MM - Product Usage: is intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin.

Insulet Corporation

FDA Devices Moderate Jun 10, 2020

Pressure Monitoring Tray, C-PMSY, G02854

Cook Inc.

FDA Devices Moderate Jun 10, 2020

Sterile Custom Packs to be used in surgical procedures.

American Contract Systems

CPSC No agency class Jun 10, 2020

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

DICK'S Sporting Goods, of Coraopolis, Pa.

CPSC No agency class Jun 10, 2020

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

CPSC No agency class Jun 10, 2020

Ushio America Recalls Indiglow LED T8 Lamps Due to Injury Hazard

NHTSA No agency class Jun 9, 2020

MERCEDES-BENZ 2019: POWER TRAIN:DRIVELINE:DRIVESHAFT

MERCEDES-BENZ

NHTSA No agency class Jun 8, 2020

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

FORD

NHTSA No agency class Jun 8, 2020

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

FORD,LINCOLN

NHTSA No agency class Jun 5, 2020

MERCEDES-BENZ 2020: SUSPENSION:REAR:SHOCK ABSORBER

MERCEDES-BENZ

NHTSA No agency class Jun 5, 2020

MERCEDES-BENZ 2020: SEATS:MID/REAR ASSEMBLY

MERCEDES-BENZ

CPSC No agency class Jun 4, 2020

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

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

CPSC No agency class 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 No agency class Jun 4, 2020

HONDA 2019: SEAT BELTS:REAR/OTHER

HONDA

NHTSA No agency class Jun 4, 2020

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

LAND ROVER

NHTSA No agency class 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 79056992863

Absorb Health LLC

FDA Food Moderate Jun 3, 2020

Wegmans Tuna & Provolone Packaged Sub, Medium, 11 oz; UPC: 2-27031-00000; SELL BY 5/14-5/16

Wegmans Food Markets, Inc.

FDA Food Moderate Jun 3, 2020

Wegmans Packaged Tuna & Provolone Wheat Wrap, 9 oz; UPC: 2-27303-00000; SELL BY 5/14-5/16

Wegmans Food Markets, Inc.

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 Pharmaceuticals Corp., Eatontown, NJ 07724.

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 53225-1023-1.

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, Woonsocket, RI 02895; NDC 66902-218-05.

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 55289-866-14), d) 20-count (NDC 55289-866-20), e) 28-count (NDC 55289-866-28), f) 30-count (NDC 55289-866-30), g) 60-count (NDC 55289-866-60), h) 120-count (NDC 55289-866-98), i) 210-count (NDC 55289-866-71), j) 300-count (NDC 55289-866-87), k) 400-count (NDC 55289-866-74), Rx only, PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127

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 10882-527-04), Manufactured for: JAR Laboratories, Elmhurst, IL.

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 repackaging by: AvKare Inc., Pulaski, TN 38478, Bulk Shipment, NDC 59746-247-97.

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 collection, transfer, and/or storage of body fluids and solid specimen samples for the purpose of laboratory testing.

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 (1) Tunneling Tool Assembly (1) Device Registration Form/Temporary Patient Identification Card (1) Manual Product Usage: Contact extension kits are part of a spinal cord stimulation system for prescription use only as an aid in the management of chronic intractable pain of the trunk and/or limbs. They are designed to connect the percutaneous leads

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 MPS Console used as replacements for worn or damaged MPS Console top covers)

Quest Medical, 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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2020

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2020 across the FDA, CPSC, USDA FSIS 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 September 2026.