PlainRecalls

2020 Recalls

5,939 recalls · Page 115 of 119

2020 Recall Year Insight

Federal agencies issued 5,939 product recalls indexed by PlainRecalls in calendar year 2020. That represents about 7.07% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 16.3 recalls per day across the FDA, CPSC, 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 119 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 11 critical, 37 moderate, and 2 lower-severity recalls. The page references 25 distinct recalling firms operating in 5 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (28), FDA Drug (14), NHTSA (4), 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Jan 22, 2020

TRIMIX FORTE PLUS 30MG/4MG/40MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

Sumatriptan Succinate Tablets, 50 mg, packaged in a) 9 (1x9) Unit-of use blister card (NDC 62756-521-69) and b) 100 count bottles, (NDC 62756-521-88)…

Sun Pharmaceutical Industries, Inc.

FDA Drug Moderate Jan 22, 2020

SUFENTANIL 300MCG/ML INJ in 20 mL syringe Assurance Infusion (713)-533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

BUP 2.5MG/FENT 25MCG/HYDRO 2MG/MORP 40MG/ML in 20 mL syringe Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

BUP 35MG/FENT 1.5MG/ML in 20 mL syringe Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

TRIMIX (UA) 30MG/1MG/20MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

TESTOSTERONE CYP 200MG/ML OIL (SESAME) INJ in 10 mL vial Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

BUP 15MG/CLON 300MCG/ FENT 1500MCG/ML(40) INJ in 20 mL syringe Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

HYDROMORPHONE 3MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

TESTOSTERONE CYP 200MG/ML OIL INJ in 10 mL vial Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

HYDROMORPHONE 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

Testosterone Cypionate for Injection, 2,000 mg/10 mL (200 mg/mL), a) 1 mL Single Use vial (NDC 62756-015-40) and b) 10 mL Multiple Dose Vial (NDC 627…

Sun Pharmaceutical Industries, Inc.

FDA Drug Moderate Jan 22, 2020

CLON 750MCG/MORP 30MG/SUF 37.5MCG/ML in 20 mL syringe Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Drug Moderate Jan 22, 2020

BAC 225MCG/ BUP 4.5MG/ CLON 9MCG/ MORP 3MG/ML ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

Assurance Infusion

FDA Devices Moderate Jan 22, 2020

Dawson-Mueller Drainage Catheter, Multipurpose Drainage Catheter, RPN UL T6.3-35-15-P-5S-CLDM-HC, UL T6. 3-35-25-P-58-CLDM-HC, UL T7.0-35-25-P-5S-CLD…

Cook Inc.

FDA Devices Moderate Jan 22, 2020

BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3, CE 0120, Do not Re-use, Rx Only, REF, 040-333U, Sterile EO, Qty 10, (01)15055788724138(…

Flexicare Medical Ltd.

FDA Devices Critical Jan 22, 2020

CARESCAPE Respiratory Module E-sCAiOV

GE Healthcare, LLC

FDA Devices Moderate Jan 22, 2020

Siemens ARTIS pheno, Model # 10849000. Interventional Fluoroscopic X-Ray System - Product Usage: Angiography system for single and biplane diagnosti…

Siemens Medical Solutions USA, Inc

FDA Devices Critical Jan 22, 2020

Airway Gas Option N-CAiO

GE Healthcare, LLC

FDA Devices Moderate Jan 22, 2020

BriteBlade Pro Single-se Fiber Optic Miller 2, CE 0120, Do not Re-use, Rx Only, REF, 040-722U, Sterile EO, Qty 10, (01) 15055788722783 The device…

Flexicare Medical Ltd.

FDA Devices Moderate Jan 22, 2020

BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2, CE 0120, Do not Re-use, Rx Only, REF: 040-342U, Sterile EO, Qty 10, UDI: (01)1505578…

Flexicare Medical Ltd.

FDA Devices Critical Jan 22, 2020

CARESCAPE Respiratory Module E-sCAiO

GE Healthcare, LLC

FDA Devices Moderate Jan 22, 2020

LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad.

Physio-Control, Inc.

FDA Devices Moderate Jan 22, 2020

Microbiologics QC Sets and Panels, Gram-Positive Blood Culture Control Panel (Inactivated Pellet), Catalog # 8180 Used in test systems to estimate t…

Microbiologics Inc

FDA Devices Moderate Jan 22, 2020

QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705

Edwards Lifesciences, LLC

FDA Devices Moderate Jan 22, 2020

BriteBlade Pro Single-Use Fiber Optic Mac 3, CE01120, Do Not Re-use, Rx Only, REF 040-713U, Sterile EO, Qty 10, (01)15055788723001 The device is …

Flexicare Medical Ltd.

FDA Devices Moderate Jan 22, 2020

Medline Thermistor Foley Catheter 14 FR 5-10 ml, non sterile Catalog Number: 102201101463MD {Medline code 55346) Monitor urinary output and bladd…

Degania Silicone, Ltd.

FDA Devices Moderate Jan 22, 2020

Gridlock Ankle Screw Driver Bit REF 320-35-003 - Product Usage: A screwdriver facilitates implant insertion and removal.

Trilliant Surgical, LLC

FDA Devices Moderate Jan 22, 2020

LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits

Physio-Control, Inc.

FDA Devices Moderate Jan 22, 2020

CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The FreeStyle Comfort Oxygen Concentrator is intended for the administration of s…

Caire, Inc.

FDA Devices Moderate Jan 22, 2020

Merlin PCS Programmer software model 3330, used with Confirm Rx Insertable Cardiac Monitor (ICM), Model DM3500, Sterile. The firm name on the label …

St Jude Medical, Cardiac Rhythm Management Division

FDA Devices Moderate Jan 22, 2020

ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula (CooperSurgical Product Code: ESPX5…

CooperSurgical, Inc.

FDA Devices Critical Jan 22, 2020

CARESCAPE Respiratory Module E-sCAiOVE

GE Healthcare, LLC

FDA Devices Low Jan 22, 2020

Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF A1500

Teleflex Medical

FDA Devices Moderate Jan 22, 2020

Kodak DirectView DR3000/3500 - Product Usage: permanently installed as a diagnostic system intended to generate and control x-rays for examination of…

Carestream Health, Inc.

FDA Devices Moderate Jan 22, 2020

Model 250D Ambulatory Blood Pressure Monitor labeled under the following brands: Bravo Mini, part number 99-0233-00; Agilis Mini, part number NJ124 …

Suntech Medical, Inc.

FDA Devices Critical Jan 22, 2020

CARESCAPE Respiratory Module E-sCAiOE

GE Healthcare, LLC

FDA Devices Critical Jan 22, 2020

CARESCAPE Respiratory Module E-sCO

GE Healthcare, LLC

FDA Devices Critical Jan 22, 2020

CARESCAPE Respiratory Module E-sCOVX

GE Healthcare, LLC

FDA Devices Moderate Jan 22, 2020

Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2…

Howmedica Osteonics Corp.

FDA Devices Moderate Jan 22, 2020

Riverpoint Medical 18G Brachy Grid, B&K style, REF RPG-18, Sterile, Rx. The firm name on the label is Riverpoint Medical, LLC, Portland, OR.

Riverpoint Medical, LLC

FDA Devices Low Jan 22, 2020

Teleflex MEDICAL RuSCH One piece Male External Medium Catheter W/O Tape, REF A1500M

Teleflex Medical

NHTSA Critical Jan 17, 2020

ACURA,HONDA 2000-2003: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

ACURA,HONDA

NHTSA Critical Jan 17, 2020

ACURA,HONDA 2000-2001: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

ACURA,HONDA

NHTSA Critical Jan 17, 2020

ISUZU 2019: SEAT BELTS:FRONT:WEBBING

ISUZU

NHTSA Critical Jan 17, 2020

HYUNDAI 2020: EQUIPMENT:OTHER:LABELS

HYUNDAI

CPSC Moderate Jan 16, 2020

Baby Trend Recalls Tango Mini Strollers Due to Fall Hazard

Baby Trend, of Fontana, Calif.

FDA Food Moderate Jan 15, 2020

GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152 00332 6 & 8 OZ (225 G) UPC 8 …

TFI Holding dba Grey Ghost Bakery

FDA Food Moderate Jan 15, 2020

Nestle Toll House Oatmeal Raisin Cookie Bar (16.5oz), UPC 050000062195

Gerber Products Company dba Nestle Infant Nutrition

FDA Food Moderate Jan 15, 2020

Nestle Toll House Peanut Butter Chocolate Chip Bar (16oz), UPC 050000622634

Gerber Products Company dba Nestle Infant Nutrition

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 — consumer product and vehicle recall feeds for 2020