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 5 critical, 43 moderate, and 2 lower-severity recalls. The page references 26 distinct recalling firms operating in 4 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (31), FDA Drug (10), FDA Food (9), 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 Food Moderate Jun 10, 2020

Dragonfly brand Galanga Powder; Net Weight: 5 oz. (142 g) UPC: 7 21557 53337 6 Product of Thailand Distributed by U.S. Trading Company, Hayward, CA 94545-1130

U.S. Tov, Inc.

FDA Food Moderate Jun 10, 2020

Cell-nique Corp

FDA Food Moderate Jun 10, 2020

Plucker's Wing Bar World Famous Wing Sauce Vampire Killer 12 FL OZ. (355 mL) packaged in a glass bottle

Zilks Foods

FDA Food Moderate Jun 10, 2020

Plucker's Wing Bar World Famous Wing Sauce Spicy Mandarin 12 FL OZ. (355 mL) packaged in a glass bottle

Zilks Foods

FDA Food Critical Jun 10, 2020

Sienna brand 4.25 oz. Cranberry Orange Muffins coded 20 071 31B

BAKE'N JOY FOODS, INC.

FDA Food Moderate Jun 10, 2020

Plucker's Wing Bar World Famous Wing Sauce Sesame 12 FL OZ. (355 mL) packaged in a glass bottle

Zilks Foods

FDA Food Moderate Jun 10, 2020

Plucker's Wing Bar World Famous Wing Sauce Teriyaki 12 FL OZ. (355 mL) packaged in a glass bottle

Zilks Foods

FDA Food Moderate Jun 10, 2020

Plucker's Wing Bar World Famous Wing Sauce Baker's Gold 12 FL OZ. (355 mL) packaged in a glass bottle

Zilks Foods

FDA Food Critical Jun 10, 2020

Organic Chipotle Chile Ground, Item # 90033. Packaged in 40 lbs. box and sold under brand Blue Chip. This product contains Chipotle Chile pepper. The Blue Chip label listed the lot # 032918. No UPC. Product distributed by Blue Chip Corp. UT.

K F K Seasonings Llc

FDA Drug Moderate Jun 10, 2020

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets ( Mixed Amphetamine Salts Product), 5 mg, 100 count bottles, Rx Only, Teva Pharmaceuticals USA, INC. North Wales, PA 19454, NDC 0555-0971-02

Teva Pharmaceuticals USA

FDA Drug Critical Jun 10, 2020

NP Thyroid 60, Thyroid Tablets, USP, 1 grain (60 mg), 100-count bottles, Rx Only, Manufactured For: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, NDC 42192-330-01.

Acella Pharmaceuticals, LLC

FDA Drug Moderate Jun 10, 2020

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets ( Mixed Amphetamine Salts Product), 15 mg, 100 count bottles, Rx Only, Teva Pharmaceuticals USA, INC. North Wales, PA 19454, NDC 0555-0777-02

Teva Pharmaceuticals USA

FDA Drug Moderate Jun 10, 2020

Estriol USP Micronized 5 G, Rx only, Triova 115 W 3rd Street Suite 720 Tulsa, OK 74103, NDC 71092-9977-02

TRIOVA PHARMACEUTICALS LLC

FDA Drug Low Jun 10, 2020

Lamotrigine Tablets, USP, 150 mg, Rx Only, a) 60 count Bottle, NDC 42291-368-60, b) 500 count Bottle, NDC 42291-368-50, Manufactured for: AvKARE, Inc. Pulaski, TN 38478.

AVKARE Inc.

FDA Drug Moderate Jun 10, 2020

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets ( Mixed Amphetamine Salts Product), 20 mg, 100 count bottles, Rx Only, Teva Pharmaceuticals USA, INC. North Wales, PA 19454, NDC 0555-0973-02

Teva Pharmaceuticals USA

FDA Drug Critical Jun 10, 2020

NP Thyroid 30, Thyroid Tablets, USP, 1/2 grain (30 mg), 100-count bottles, Rx Only, Manufactured For: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, NDC 42192-329-01.

Acella Pharmaceuticals, LLC

FDA Drug Moderate Jun 10, 2020

Doxycycline Hyclate Tablets, USP, 100 mg, packaged in a) 3x10 unit dose cartons (NDC 0904-0430-04) and b) 5 x 10 unit dose carton (NDC 0904-0430-06), Mfd. by: West-Ward Pharmaceutical Corp., Eatontown, NJ 07724; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152.

The Harvard Drug Group

FDA Drug Critical Jun 10, 2020

NP Thyroid 90, Thyroid Tablets, USP, 1 & 1/2 grain (90 mg), 100-count bottles, Rx Only, Manufactured For: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, NDC 42192-331-01.

Acella Pharmaceuticals, LLC

FDA Drug Moderate Jun 10, 2020

Carbamazepine Tablets, USP 200 mg, packaged in a 500-count bottle, Rx only, Manufactured by: Torrent Pharmaceuticals Ltd, Bharuch 392130, India; Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920, NDC 13668-268-05

Torrent Pharma Inc.

FDA Devices Moderate Jun 10, 2020

TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: is intended for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertip or forearm.

Trividia Health, Inc.

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X35MM, Item Number 810M5535 - 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 4.5X45MM, Item Number 810M4545 - 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 Low Jun 10, 2020

PerkinElmer 226 Sample Collection Device

PerkinElmer Health Sciences, Inc.

FDA Devices Moderate Jun 10, 2020

Sterile Custom Packs to be used in surgical procedures.

American Contract Systems

FDA Devices Moderate Jun 10, 2020

Sterile Custom Packs to be used in surgical procedures.

American Contract Systems

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X55MM, Item Number 811M8555 - 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

AC Powered hospital adjustable bed.

Umano Medical, Inc.

FDA Devices Moderate Jun 10, 2020

Sterile Custom Packs to be used in surgical procedures.

American Contract Systems

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X50MM, Item Number 810M5550 - 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 5.5X45MM, Item Number 810M5545 - 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

Beckman Coulter ACCESS Immunoassay Systems, Access Total T3 Triiodothyronine , REF 33830 (UDI: 15099590227210) for use with the Access Family of Immunoassay Systems including: Access 2, UniCel DxI 600, UniCel DxI 800, UniCel DxC 600i, UniCel DxC 660i, UniCel DxC 680i, UniCel DxC 860i, and UniCel DxC 880i systems.

Beckman Coulter Inc.

FDA Devices Moderate Jun 10, 2020

Gambro Cartridge Low Weight-Low Volume Blood Transport System for Hemodialysis Blood Set - Product Usage: is intended for single use in a hemodialysis treatment using Dialysis Delivery Systems.

Baxter Healthcare Corporation

FDA Devices Moderate Jun 10, 2020

Beckman Coulter ACCESS Immunoassay Systems, Access GI Monitor Cancer Antigen 19-9, REF 387687 ( UDI: 15099590231842) the Access Family of Immunoassay Systems including: Access 2, UniCel DxI 600, UniCel DxI 800, UniCel DxC 600i, UniCel DxC 660i, UniCel DxC 680i, UniCel DxC 860i, and UniCel DxC 880i systems.

Beckman Coulter Inc.

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X60MM, Item Number 811M8560 - 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

safeCLINITUBES Blood Sampler;REF 942-898;D957P-70-70x1

Radiometer Medical ApS

FDA Devices Moderate Jun 10, 2020

OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - 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

Pressure Monitoring Set, C-PMS, G02838

Cook Inc.

FDA Devices Moderate Jun 10, 2020

Beckman Coulter ACCESS Immunoassay Systems, Access Thyroglobulin, REF 33860 (UDI: 15099590227173) for use with the Access Family of Immunoassay Systems including: Access 2, UniCel DxI 600, UniCel DxI 800, UniCel DxC 600i, UniCel DxC 660i, UniCel DxC 680i, UniCel DxC 860i, and UniCel DxC 880i systems.

Beckman Coulter Inc.

FDA Devices Moderate Jun 10, 2020

Medtronic Implantable Insulin Pump System, REF: MMT-2007D, Sterile EO, CE 0459 UDI: 00763000043001

Medtronic Inc.

FDA Devices Moderate Jun 10, 2020

OSTEOVATION 5CC IMPACTFORMULA. REF/UDI: 390-2105/00813845020085 - 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

NobelActive Internal NP 3.5x15mm Endosseus dental implant, REF: 34128, Rx Only, Sterile R, CE, UDI: (01)07332747010619

Nobel Biocare Usa Llc

FDA Devices Moderate Jun 10, 2020

ARTIS icono systems with Quantification Application SW (QVA/QCA) on a standalone XWP computer, an interventional Fluoroscopic X-Ray System Model Number: 11327600

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jun 10, 2020

Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X40MM, Item Number 810M6540 - 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 6.5X55MM, Item Number 810M6555 - 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

da Vinci SP surgical system

Intuitive Surgical, Inc.

FDA Devices Moderate Jun 10, 2020

safeCLINITUBES Blood Sampler;REF 942-969;D957P-70-45x1

Radiometer Medical ApS

FDA Devices Moderate Jun 10, 2020

Sterile Custom Packs to be used in surgical procedures.

American Contract Systems

FDA Devices Moderate Jun 10, 2020

OSTEOVATION RMX Injectable BVF 5CC . REF/UDI: 390-6001/ /00813845021082 - 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 POLY EXT TAB 4.5X35MM, Item Number 810M4535 - 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 a3600 Automation System using the Aliquoter Module (Inpeco P/N FLX-212) - Product Usage: The systems consolidate multiple Analytical instruments into a unified workstation.

Inpeco S.A.

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.