PlainRecalls

2020 Recalls

5,939 recalls · Page 97 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, 39 moderate, and 0 lower-severity recalls. The page references 15 distinct recalling firms operating in 1 distinct product categories, with 48 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 26, 2020

Polysorb Braided Absorbable Suture 2/0 UNDYED 30" V-30 (75CM), Item Code GL228 - Product Usage: Indicated for use in soft tissue approximation or lig…

Covidien LLC

FDA Devices Moderate Feb 26, 2020

Arrow EPIDURAL CATHETERIZATION KIT CK-02220

Arrow International Inc

FDA Devices Critical Feb 26, 2020

NC TREK Coronary Dilatation Catheter, REF 1012454-15 Rx Only, NC TREK RX 4.50 X 15MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated…

Abbott Vascular

FDA Devices Moderate Feb 26, 2020

Philips HeartStart FRx AED, Model 861304, FRx codeRev: E.02.017

Philips North America LLC

FDA Devices Moderate Feb 26, 2020

(1) Arrow¿ STIM CPNB TUOHY NDL: 18G x 14CM (5-1/2") AB-18140-N (2) Arrow¿ STIM CPNB TUOHY NDL: 18G x 11CM (4-3/8") AB-18110-N (3) Arrow¿ STIM CPN…

Arrow International Inc

FDA Devices Critical Feb 26, 2020

Trilogy EVO Ventilator, Germany - Model Number: DE2110X13B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. …

Philips Respironics, Inc.

FDA Devices Critical Feb 26, 2020

Trilogy EVO Ventilator, 02 - Iberia - Model Number: ES2100X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 …

Philips Respironics, Inc.

FDA Devices Critical Feb 26, 2020

Trilogy EVO Ventilator, Great Britain - Model Number: GB2110X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.…

Philips Respironics, Inc.

FDA Devices Moderate Feb 26, 2020

Polysorb Braided Absorbable Suture 2-0 VIOLET 30" V-20, Item Code GL123 - Product Usage: Indicated for use in soft tissue approximation or ligation a…

Covidien LLC

FDA Devices Moderate Feb 26, 2020

Polysorb Braided Absorbable Suture 2-0 VIOLET 36" GS-21, Item Code CL923 - Product Usage: Indicated for use in soft tissue approximation or ligation …

Covidien LLC

FDA Devices Moderate Feb 26, 2020

SnapLink, Ref Part No. 438-2191, L6L SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx Only

Ormco/Sybronendo

FDA Devices Critical Feb 26, 2020

Trilogy EVO Ventilator, International, Model Number IN2110X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 …

Philips Respironics, Inc.

FDA Devices Critical Feb 26, 2020

Trilogy EVO Ventilator, 02 - Italy - Model Number: IT2100X21B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 k…

Philips Respironics, Inc.

FDA Devices Critical Feb 26, 2020

NC TREK Coronary Dilatation Catheter, REF 1012453-12 Rx Only, NC TREK RX 4.00 X 12MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated…

Abbott Vascular

FDA Devices Moderate Feb 26, 2020

Dimension Enzymatic Creatinine (EZCR) reagent, SMN 10471520

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Feb 26, 2020

Polysorb Braided Absorbable Suture 2-0 UNDYED 36" GS-21, Item Code CL953 - Product Usage: Indicated for use in soft tissue approximation or ligation …

Covidien LLC

FDA Devices Moderate Feb 26, 2020

Polysorb Braided Absorbable Suture 0 VIOLET 30" V-20, Item Code GL124 - Product Usage: Indicated for use in soft tissue approximation or ligation and…

Covidien LLC

FDA Devices Moderate Feb 26, 2020

Drill Tapered WP 5x11.5 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to i…

Nobel Biocare Usa Llc

FDA Devices Moderate Feb 26, 2020

Polysorb Braided Absorbable Suture UD 3/0 30 P-14, Item Code SL5679 - Product Usage: Indicated for use in soft tissue approximation or ligation and o…

Covidien LLC

FDA Devices Moderate Feb 26, 2020

1 STRATAFIX" Spiral PDS Plus Violet 36" (90cm) CTX Needle, SXPP1B402

Ethicon, Inc.

FDA Devices Moderate Feb 26, 2020

Teleflex Medical Disposable Aortic Punch, in the following sizes: a) 2.8 mm, REF DP-28K b) 3.6 mm, REF DP-36K c) 4.0 mm, REF DP-40K d) 4.4 mm, RE…

TELEFLEX MEDICAL INC

FDA Devices Moderate Feb 26, 2020

Arrow Maximal Barrier Drape ASK-00002-1A

Arrow International Inc

FDA Devices Critical Feb 26, 2020

NC TREK Coronary Dilatation Catheter, REF 1012454-20 Rx Only, NC TREK RX 4.50 X 20MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated…

Abbott Vascular

FDA Devices Moderate Feb 26, 2020

Pentax Video Colonoscope Model: EC38-i10L

Pentax of America Inc

FDA Devices Moderate Feb 26, 2020

1 STRATAFIX" Spiral PDS Plus Violet 12" (30 cm) CT-1 Needle, SXPP1B429

Ethicon, Inc.

FDA Devices Moderate Feb 26, 2020

Luminos Agile Max, Model No. 10762472 - Product Usage: Luminos Agile Max is a device intended to visualize anatomical structures by converting an X-r…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 26, 2020

Arrow Pressure Injectable Two-Lumen PICC Kit 5 Fr. x 50 cm EU-05052-HPMSB

Arrow International Inc

FDA Devices Moderate Feb 26, 2020

Arrow EPIDURAL CATHETERIZATION KIT AM-05500

Arrow International Inc

FDA Devices Critical Feb 26, 2020

NC TRAVELER Coronary Dilatation Catheter, REF 1013157-08, Rx Only,NC Traveler RX 4.0 X 8MM The NC Traveler RX Coronary Dilatation Catheter is not…

Abbott Vascular

FDA Devices Moderate Feb 26, 2020

Drill Tapered 6.0 6x8 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to imp…

Nobel Biocare Usa Llc

FDA Devices Moderate Feb 26, 2020

Dense Bone Drill NP 3.5x16 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior t…

Nobel Biocare Usa Llc

FDA Devices Moderate Feb 26, 2020

Luminos Agile Max, model no. 10762471 - Product Usage: Luminos Agile Max is a device intended to visualize anatomical structures by converting an X-r…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 26, 2020

Pentax Video Colonoscope Model: EC34-i10L

Pentax of America Inc

FDA Devices Moderate Feb 26, 2020

ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000 - Product Usage:AXIOM Artis is a family of dedicated angiography systems…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 26, 2020

EDAN Telemetry Transmitter, Model iT20 - Product Usage: The iT20 telemetry transmitter is intended to be used in clinical divisions of hospital envir…

Edan Diagnostics

FDA Devices Moderate Feb 26, 2020

Implant Retrieval Instrument CC NP & Ext Hex WP 22 mm - Product Usage: They can be used to remove implants, if the implant connection has been damage…

Nobel Biocare Usa Llc

FDA Devices Moderate Feb 26, 2020

CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Feb 26, 2020

Polysorb Braided Absorbable Suture UD 4/0 18 P-13, Item Code SL5690 - Product Usage: Indicated for use in soft tissue approximation or ligation and o…

Covidien LLC

FDA Devices Critical Feb 26, 2020

NC TREK Coronary Dilatation Catheter, REF 1012455-120 Rx Only,NC TREK RX 5.00 X 20MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated…

Abbott Vascular

FDA Devices Moderate Feb 26, 2020

Luminos dRF Max, Model No. 10762471 - Product Usage: Luminos dRF Max is a device intended to visualize anatomical structures by converting an X-ray p…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 26, 2020

Arrow SPINAL ANESTHESIA SET ASA-25090-S

Arrow International Inc

FDA Devices Moderate Feb 26, 2020

Implant Retrieval Instrument CC 3.0 31 mm- Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be …

Nobel Biocare Usa Llc

FDA Devices Moderate Feb 26, 2020

Luminos dRF Max, model no. 10762471 - Product Usage: Luminos dRF Max is a device intended to visualize anatomical structures by converting an X-ray p…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 26, 2020

DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic Diagnostic Imaging System is appli…

Mindray DS USA, Inc. dba Mindray North America

FDA Devices Moderate Feb 26, 2020

Implant Retrieval Instrument CC RP & Tri Ch Hex WP 22 mm - Product Usage: They can be used to remove implants, if the implant connection has been da…

Nobel Biocare Usa Llc

FDA Devices Moderate Feb 26, 2020

Arrow EPIDURAL NEEDLE KIT SL-05500

Arrow International Inc

FDA Devices Moderate Feb 26, 2020

Drill Tapered RP 4.3x10 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotom…

Nobel Biocare Usa Llc

FDA Devices Critical Feb 26, 2020

NC TREK Coronary Dilatation Catheter, REF 1012453-08 Rx Only, NC TREK RX 4.00 X 8MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated …

Abbott Vascular

FDA Devices Moderate Feb 26, 2020

Implant Retrieval Instrument Hex & Tri-Ch NP/RP 22mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged…

Nobel Biocare Usa Llc

FDA Devices Moderate Feb 26, 2020

Uroskop Omnia max, Model No. 10762473 - Product Usage: Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an Xra…

Siemens Medical Solutions 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: CPSC + NHTSA — consumer product and vehicle recall feeds for 2020