PlainRecalls

2020 Recalls

5,939 recalls · Page 100 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 5 critical, 44 moderate, and 1 lower-severity recalls. The page references 19 distinct recalling firms operating in 1 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRH

Arrow International Inc

FDA Devices Critical Feb 19, 2020

Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and Canada Version Only

Medtronic Inc.

FDA Devices Moderate Feb 19, 2020

Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Single, REF 3910-500-471, UDI 07613327464818, Sterile R, RX Only CE 0197

Stryker Corporation

FDA Devices Moderate Feb 19, 2020

Implant Direct, CE 0086, REF: 855710, Legacy 3 Impant, Surface: SBM, Qty:1, Size:5.7mmD x 10mmL, 5.7mmD Platform, RxOnly, Sterile R,

Implant Direct Sybron Manufacturing LLC

FDA Devices Critical Feb 19, 2020

Medtronic MiniMed 640G Insulin Infusion Pump, Ref#s/Model(s) - MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1751, and MMT-1752 *Not for US Distribut…

Medtronic Inc.

FDA Devices Moderate Feb 19, 2020

Button-Style Ultrasound Transducer (Nautilus), 8-foot Cord 5700HAX, that may have been serviced with the following: Pacific Medical GE Corometrics Na…

Pacific Medical Group Inc.

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05500-TM

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BE-05400B-ETTEL

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended wear)

CooperVision Inc.

FDA Devices Moderate Feb 19, 2020

Respironics V60 Ventilator, Service # 850008, REF: 1053613, 1053614, 1053617, 1053614

Respironics California, LLC

FDA Devices Moderate Feb 19, 2020

Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System

TELEFLEX MEDICAL INC

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code UR-05501

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code CA-02220

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-12

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LEO

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code ASK-17019-MSC

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

Toco M2734A, that may have been serviced with the following: Pacific Medical Philips Avalon Smart US/TOCO Cable Assembly, NFPHA9020; Pacific Medical …

Pacific Medical Group Inc.

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BE-080180-CHH

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

Prometra II 20mL Pump. Catalog No. 13827 The device is an implantable infusion pump. GTIN-14 00810335020228

Flowonix Medical Inc

FDA Devices Critical Feb 19, 2020

HUDSON RCI COMFORT FLO Corrugated Humidification System, REF 2415, humidifier nebulizer kit

TELEFLEX MEDICAL INC

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-FR1

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BJC-05400-BEN

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code MTO-05500-SU

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and VITROS 5600/XT 7600 Integrat…

Ortho Clinical Diagnostics Inc

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code AK-05500

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

fridababy SmileFrida the TOOTHHUGGER 18+ months Triple Angle Brush Cleans All Sides at Once

Fridababy LLC

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-10

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

Loop-Style Ultrasound Transducer (Nautilus), 8-foot Cord 5700LAX, that may have been serviced with the following: Pacific Medical GE Corometrics Naut…

Pacific Medical Group Inc.

FDA Devices Moderate Feb 19, 2020

Prometra Programmable 20mL Pump. Catalog No. 91827 The device is an implantable infusion pump. GTIN-14 00810335020XXX (XXX = in-country language spec…

Flowonix Medical Inc

FDA Devices Moderate Feb 19, 2020

Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 07613327464832, Sterile R, RX Only CE 0197

Stryker Corporation

FDA Devices Moderate Feb 19, 2020

Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot Plating System, a plate and scre…

Nextremity Solutions

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Set, Product Code MTO-05500-TK

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

ROSA One 3.1 Brain Application

MEDTECH SAS

FDA Devices Moderate Feb 19, 2020

Terumo Advanced Perfusion Assembly Pump Guts, 4 Inch, Catalog Number 801805 - Product Usage: is indicated for use for up to 6 hours in the extracorpo…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Feb 19, 2020

Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010

Medicrea International

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-WH

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LIN

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

Epidural Catheterization Kit with FlexTip Plus Catheter, Product Code TI-05520-EPI

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05501-SH

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-TG1

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCSHO

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code MP-17019-TKP

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

Revanesse Versa, PN40081

Prollenium Medical Technologies Inc.

FDA Devices Low Feb 19, 2020

LivaNova Sorin Connect DPIII KOMPL. S5 REF 96-415-130, 2017-08-15, IPX1, RXOnly, (01)04033817901594 Product Usage: The S5 System is used to perfo…

LivaNova USA Inc.

FDA Devices Moderate Feb 19, 2020

Blue Ortho TKA Pro v2.1 software installed on the Exactech GPS system -indicated for stereotaxic surgery in Knee Arthroplasty Catalog Reference: L00…

Blue Ortho

FDA Devices Critical Feb 19, 2020

Medtronic MiniMed 620G Insulin Infusion Pump, Ref #s/Model(s) - MMT-1510, MMT-1710, and MMT-1750 *Not Distributed within the US

Medtronic Inc.

FDA Devices Moderate Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B

Arrow International Inc

FDA Devices Moderate Feb 19, 2020

VNS Therapy SENTIVA Generator Model # 1000 Labeling 26-0009-6800 Model 1000 Generator Sample Labels 26-0009-9600 Patient s Manual for Depressio…

LivaNova USA Inc

FDA Devices Moderate Feb 19, 2020

Terumo Advanced Perfusion System 1 Roller Pump, 4 Inch, Catalog Number 816570 - Product Usage: is indicated for use for up to 6 hours in the extracor…

Terumo Cardiovascular Systems Corporation

FDA Devices Critical Feb 19, 2020

Medtronic MiniMed 670G System with SmartGuard, Ref #s/Model Number(s) - MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1580, MMT-1581, MMT-15…

Medtronic 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 — consumer product and vehicle recall feeds for 2020