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 2 critical, 46 moderate, and 2 lower-severity recalls. The page references 20 distinct recalling firms operating in 5 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (42), FDA Drug (5), FDA Food (2), 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.

USDA FSIS Critical Jul 30, 2020

JBS Food Canada ULC Recalls Raw Boneless Beef Products Distributed without Benefit of Import Re-inspection

Balter Meat Company

FDA Food Moderate Jul 29, 2020

Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM

Cj Haide (Ningbo) Biotech Co., Ltd

FDA Food Moderate Jul 29, 2020

Red Velvet Layered Cheesecake is one whole cake (9" round cake) that has been pre-sliced into 14 slices and packaged in a white case box. Cheesecake is wrapped in a white band, ran through a shrink wrap machine and then put in a white case pack. Net weight: 82 oz. UPC 603812924900. Product must be stored frozen until use or refrigerated for up to 10 days. The cake is frosted with cream cheese frosting, coated in red velvet crumbs and then topped with White Chocolate Blossoms. The rec

Chuckanut Bay Foods LLC

FDA Drug Moderate Jul 29, 2020

Walker Emulsions Hand Sanitizer (60%), Non-Sterile Solution, Alcohol Antiseptic 60%, 1 Gallon, Topical Solution, Walker Emulsions Inc., 4401 SE Johnson Creek Blvd., Portland, OR 97222, NDC 74940-0415-1

WALKER EMULSIONS INC

FDA Drug Moderate Jul 29, 2020

Cefdinir for Oral Suspension USP, 250 mg/5mL, packaged in 60 mL bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland, Manufactured by: Lupin Limited, Mandideep, India, NDC 68180-723-20

Lupin Pharmaceuticals Inc.

FDA Drug Low Jul 29, 2020

Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only After Dilution, Distributed by HF Acquisition Co, LLC, Mukilteo, WA 98275, NDC 63323-739-12

HF Acquisition Co. LLC

FDA Drug Critical Jul 29, 2020

Mystic Shield PROTECTION, ALCOHOL ANTISEPTIC 70%, Topical Solution, Antiseptic Hand Rub, Non-sterile Solution, Extra strength Formula*, 8.45 fl. oz. (250 ml) bottle, Labeled with green or blue labels, Manufactured by Mystic Intl S.A. de C.V. UPC barcode: 7 87790 33952 6

Transliquid Technologies, LLC

FDA Drug Moderate Jul 29, 2020

Walker Hand Sanitizer, Non-Sterile Solution, Alcohol Antiseptic, 70%, 32 oz and 16 oz, Topical Solution, Walker Emulsions Inc., 4401 SE Johnson Creek Blvd., Portland, OR 97222, NDC 74940-0415-1

WALKER EMULSIONS INC

FDA Devices Moderate Jul 29, 2020

Ablation Galil Technology, IcePearl¿2.1 CX Prostate¿Kit Visual Ice System, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.

Boston Scientific Corporation

FDA Devices Moderate Jul 29, 2020

Ablation Galil Technology, Three IceFORCE 2.1 CX Prostate Cyroablation Kit Visual ICE System, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.

Boston Scientific Corporation

FDA Devices Moderate Jul 29, 2020

Safe-T PLUS Thora-Para 5 Fr Catheter Drainage Tray

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

PowerLoc MAX Power Injectable Infusion Port Access Kit; Catalog Numbers 2131910 (UDI 00801741044151), 2131915 (UDI 00801741044168), 2131975 (UDI 00801741044175), 2132010 (UDI 00801741044151), 2132015 (UDI 00801741044199), 2132075 (UDI 00801741044205), 2132210 (UDI 00801741044212), 2132275 (UDI 00801741044236), 2141910 (UDI 00801741044243), 2141915 (UDI 00801741044250), 2141975 (UDI 00801741044267), 2142010 (UDI 00801741044274), 2142015 (UDI 00801741044281), 2142075 (UDI 00801741044298), 2142210

Becton Dickinson & Company

FDA Devices Moderate Jul 29, 2020

Ablation Galil Technology, IcePearl 2.1 CX Needle Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.

Boston Scientific Corporation

FDA Devices Moderate Jul 29, 2020

SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing; Catalog Number CPA00040 (UDI 00801741143892)

Becton Dickinson & Company

FDA Devices Moderate Jul 29, 2020

PowerLoc MAX Power Injectable Infusion Set; Catalog Numbers 0131910 (UDI 00801741047329), 0131915 (UDI 00801741047336), 0131975 (UDI 00801741047343), 0132010 (UDI 00801741047350), 0132015 (UDI 00801741047367), 0132075 (UDI 00801741047374), 0132210 (UDI 00801741047381), 0132215 (UDI 00801741047398), 0132275 (UDI 00801741047404), 0141910 (UDI 00801741047411), 0141915 (UDI 00801741047428), 0141975 (UDI 00801741047435), 0142010 (UDI 00801741047442), 0142015 (UDI 00801741047459), 0142075 (UDI 00801

Becton Dickinson & Company

FDA Devices Moderate Jul 29, 2020

SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit; Catalog Numbers PA-0031G (UDI 00801741085666), PA-0031YNG (UDI 00801741085673), PA-0032G (UDI 00801741087639), PA-0033G (UDI 00801741096433)

Becton Dickinson & Company

FDA Devices Moderate Jul 29, 2020

LoFric Origo, Tiemann, 16in, FR12 urinary catheters

Wellspect HealthCare (Division of DENTSPLY IH AB)

FDA Devices Moderate Jul 29, 2020

SafeStep Huber Needle Set Port Access Kit; Catalog Numbers PA-0029 (UDI 00801741085482), PA-0029YN (UDI 00801741085499), PA-0030 (UDI 00801741085505), PA-0030YN (UDI 00801741085512), PA-0031 (UDI 00801741085529), PA-0031YN (UDI 00801741085536), PA-0032 (UDI 00801741085543), PA-0032YN (UDI 00801741085550), PA-0033 (UDI 00801741085567), PA-0033YN (UDI 00801741085574), PA-0034 (UDI 00801741085581), PA-0034YN (UDI 00801741085598), PA-0036 (UDI 00801741085604), PA-0038 (UDI 00801741085628), PA-0038YN

Becton Dickinson & Company

FDA Devices Moderate Jul 29, 2020

PowerLoc MAX Power-Injectable Infusion Set myPICK Port Access Kit; Catalog Numbers CPA00001 (UDI 00801741098345), CPA00002 (UDI 00801741098352), CPA00028 (UDI 00801741129728), CPA00032 (UDI 00801741137501), CPA00033 (UDI 00801741137501), CPA00036 (UDI 00801741138911), CPA00051 (UDI 00801741175718), CPA00055 UDI 00801741182181), CPA00056 (UDI 00801741182907)

Becton Dickinson & Company

FDA Devices Moderate Jul 29, 2020

PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Catalog Numbers AN132075 (UDI 00801741118968), AN142010 (UDI 00801741119231), AN142010G (UDI 00801741119323), AN142075 (UDI 00801741119224)

Becton Dickinson & Company

FDA Devices Moderate Jul 29, 2020

Accurian RF Ablation, Cannula pk, Accurian, 150mm, 20G, 10mm, CS Product Number: AC0012 GTIN / UPN: 20763000153629 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting, and a stylet with a color-coded cap to indicate gauge size. The ACCURIAN RF Cannula included in the ACCURIAN RF Ablation Platform intended for the creation of radiofrequency lesions in nervous tissue.

Medtronic Sofamor Danek USA Inc

FDA Devices Moderate Jul 29, 2020

TRIGEN, Intramedullary nail - Product Usage: is intended to provide resistance for screw back-out. It provides additional friction to help hold the screws in place.

Smith & Nephew, Inc.

FDA Devices Moderate Jul 29, 2020

SafeStep Huber Needle Set with Y Injection Site and Medegen Needleless Injection Cap; Catalog Numbers LH-0029YN (UDI 00801741066177), LH-0030YN (UDI 00801741066191), LH-0031YN (UDI 00801741066214), LH-0032YN (UDI 00801741066238), LH-0033YN (UDI 00801741066252), LH-0034YN (UDI 00801741066276), LH-0035YN (UDI 00801741066290 ), LH-0036YN (UDI 00801741066313), LH-0037YN (UDI 00801741066337), LH-0038YN (UDI 00801741066351), LH-0039YN (UDI 00801741066313), LH-0040YN (UDI 00801741066399)

Becton Dickinson & Company

FDA Devices Moderate Jul 29, 2020

ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM

U&I CORP.

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis PLUS 8 Fr Catheter Drainage Tray

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product Usage: is a fully automated, user configurable, open system intended for use to prepare human specimens for subsequent analysis on flow cytometers.

Sysmex America, Inc.

FDA Devices Moderate Jul 29, 2020

Ablation Galil Technology, IceFORCE 2.1 CX 90 Needle Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.

Boston Scientific Corporation

FDA Devices Moderate Jul 29, 2020

LoFric Origo, Tiemann, 16in, FR14 urinary catheters

Wellspect HealthCare (Division of DENTSPLY IH AB)

FDA Devices Moderate Jul 29, 2020

MEVION S250 Proton Radiation Treatment System; intended to deliver proton radiation treatment to patients

Mevion Medical Systems, Inc.

FDA Devices Moderate Jul 29, 2020

Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal, drilling and sawing of soft and hard tissue and bone in surgical procedures.

Medtronic Xomed, Inc.

FDA Devices Moderate Jul 29, 2020

Safe-T PLUS Thora-Para 8 Fr Catheter Drainage Tray

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

Thora-Para 5 Fr Catheter Drainage Tray

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

Ablation Galil Technology, IceForce 2.1 CX 90 Cyroablation Needles, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.

Boston Scientific Corporation

FDA Devices Moderate Jul 29, 2020

Ablation Galil Technology, IceFORCE 2.1 CX Prostate Kit Visual ICE System, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.

Boston Scientific Corporation

FDA Devices Moderate Jul 29, 2020

LoFric Origo, Nelaton, 16in, FR10 urinary catheters

Wellspect HealthCare (Division of DENTSPLY IH AB)

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis 6 Fr Catheter Drainage Tray w/o Lidocaine

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended for intraoperative neurophysiologic monitoring during spinal surgery.

NuVasive Inc

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis 8 Fr Catheter Drainage Tray

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

Safe-T PLUS Thora-Para 5 Fr Non-Valved Catheter Drainage Tray

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

Accurian RF Ablation, Cannula pk, Accurian, 100mm, 22G, 5mm, CS Product Number: AC0016 GTIN / UPN: 20763000153674 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting, and a stylet with a color-coded cap to indicate gauge size. The ACCURIAN RF Cannula included in the ACCURIAN RF Ablation Platform intended for the creation of radiofrequency lesions in nervous tissue.

Medtronic Sofamor Danek USA Inc

FDA Devices Low Jul 29, 2020

LivaNova USA Sterile Disposable Connector,1/2x1/2, 20 units per case

LivaNova USA Inc.

FDA Devices Moderate Jul 29, 2020

Accurian RF Ablation,Cannula pk, Accurian, 100mm, 22G, 10mm, SS Product Number: AC0019 GTIN / UPN: 20763000153667 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting, and a stylet with a color-coded cap to indicate gauge size. The ACCURIAN RF Cannula included in the ACCURIAN RF Ablation Platform intended for the creation of radiofrequency lesions in nervous tissue.

Medtronic Sofamor Danek USA Inc

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis PLUS 6 Fr Catheter Drainage Tray

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

Thora-Para 8 Fr Catheter Drainage Tray w/o Lidocaine

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

Safe-T-Centesis 6 Fr Catheter Drainage Tray

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

Thora-Para 8 Fr Catheter Drainage Tray

Carefusion 2200 Inc

FDA Devices Moderate Jul 29, 2020

IntelliVue MX800 patient monitor, model no. 865240

Philips North America, LLC

FDA Devices Moderate Jul 29, 2020

Accurian RF Ablation, Cannula pk, Accurian, 100mm, 20G, 10mm, CS Product Number: AC0009 GTIN / UPN: 20763000153599 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting, and a stylet with a color-coded cap to indicate gauge size. The ACCURIAN RF Cannula included in the ACCURIAN RF Ablation Platform intended for the creation of radiofrequency lesions in nervous tissue.

Medtronic Sofamor Danek USA Inc

FDA Devices Moderate Jul 29, 2020

Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.

Boston Scientific Corporation

FDA Devices Moderate Jul 29, 2020

Accurian RF Ablation, Cannula pk, Accurian, 150mm, 18G, 10mm, CS Product Number: AC0007 GTIN / UPN: 20763000153568 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting, and a stylet with a color-coded cap to indicate gauge size. The ACCURIAN RF Cannula included in the ACCURIAN RF Ablation Platform intended for the creation of radiofrequency lesions in nervous tissue.

Medtronic Sofamor Danek USA 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.