PlainRecalls

2020 Recalls

4,819 recalls · Page 57 of 97

2020 Recall Year Insight

Federal agencies issued 4,819 product recalls indexed by PlainRecalls in calendar year 2020. That represents about 5.74% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 13.2 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 97 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 1 critical, 47 moderate, and 2 lower-severity recalls. The page references 22 distinct recalling firms operating in 3 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (48), FDA Drug (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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate May 13, 2020

Infuvite PEDiatric Pharmacy, kit in 1 carton (40 mL fill in a 50 mL) vial 1 and (10 mL) in vial 2, Rx Only, Distributed by: Baxter Healthcare Corp…

Sandoz, Inc

FDA Drug Moderate May 13, 2020

Epinephrine Injection USP, 0.3 mg (Auto-Injector), 0.3 mg/ 0.3 mL pre-filled syringe, Rx Only, Manufactured for Teva Pharmaceuticals USA, Inc. North …

Teva Pharmaceuticals USA

FDA Devices Moderate May 13, 2020

Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf and…

Inpeco S.A.

FDA Devices Critical May 13, 2020

Python Embolectomy Catheters, Sterile EO, CE, Ref numbers/UDI: A4E01/(01)00607915113407; A4E02/(01)00607915113414; A4E03/(01)00607915113421; A4E04…

Applied Medical Resources Corp

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175912P0 - Product Usage: for use in the replacement or repair o…

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175930P0 - Product Usage: for use in the replacement or repair o…

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175826P0 - Product Usage: for use in the replacement or repair o…

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

The Cogent Hemodynamic Monitoring System. REF58400-000, GTIN 00840619099459; REF 58400-000R, GTIN 0087709094314; REF 58403, GTIN 00840619079505; REF …

ICU Medical, Inc.

FDA Devices Moderate May 13, 2020

Esthetic Abutment CC RP 1.5 mm pre-manufactured prosthetic components directly connected to the endosseous implant, catalog no. 36669 - Product Usage…

Nobel Biocare Usa Llc

FDA Devices Moderate May 13, 2020

REF: Z2812, 121" 10 Drop Primary Set w/5 MicroClave, Remv 2 Gang 4-Way Stopcocks, Rotating Luer, 2 Ext, Sterile R, UDI: (01)00887709028074

ICU Medical, Inc.

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175822P0 - Product Usage: for use in the replacement or repair …

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

Ivoclar Vivadent IPS e.max ZirCAD CER/inLab Start.Kit LT - ceramic for dental use, intended for IPS e.max ZirCAD presintered yttrium oxide-stabilize…

Ivoclar Vivadent AG

FDA Devices Moderate May 13, 2020

Hemashield Gold Knitted Microvel Double Velour Vascular Graft Axillo-bifemoral, Product Code: M002020955890 - Product Usage: for use in the replaceme…

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - ceramic for dental use,intended for IPS e.max ZirCAD presintered yttrium oxide-stabilized …

Ivoclar Vivadent AG

FDA Devices Moderate May 13, 2020

REF: Z2560, 100" 10 Drop Admin Set w/Hand Pump, 2 Clave", Rotating Luer, 1 Pressure Infusion (400psig) Ext, Purple Clamp, UDI: (01)(01)00887709026889

ICU Medical, Inc.

FDA Devices Moderate May 13, 2020

daVinci XI Sureform 60 Reload, 60 mm black 6-Row 4.6 mm, Ref: 48360T-08 , UDI: 00886874113851, Rx only, SterileEO - Product Usage: are intended to b…

Intuitive Surgical, Inc.

FDA Devices Moderate May 13, 2020

Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.

Ortho Development Corporation

FDA Devices Moderate May 13, 2020

Philips Brilliance iCT SP Computed Tomography X-Ray System; Model # 728311

Philips North America, LLC

FDA Devices Moderate May 13, 2020

Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing containing hydrogel and honey (100% Leptospermum honey), Model Number:GEN-1…

Gentell, Inc

FDA Devices Moderate May 13, 2020

Temporary Abutment Engaging CC RP pre-manufactured prosthetic components directly connected to the endosseous implant, catalog no. 36664 - - Product …

Nobel Biocare Usa Llc

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175730AP0 - Product Usage: for use in the replacement or …

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

Visualase Cooled Laser Applicator System Tubing Set kits Product numbers: VCLAS 9735559, 3mm tip/1.65mm catheter VCLAS 9735560, 10mm tip/1.65mm …

Medtronic Navigation, Inc.

FDA Devices Moderate May 13, 2020

NobelParallel Conical Connection NP, 3.75x10mm (Endosseous Dental Implant); REF 37965; UDI (01)07332747091441(10)12129104(17)240203 - Product Usage:…

Nobel Biocare Usa Llc

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft01 Branch, Product Code: M00202175834P0 - Product Usage: for use in the replacement or repair o…

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175832P0 - Product Usage: for use in the replacement or repair o…

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

Philips Brilliance iCT Computed Tomography X-Ray System; Model # 728306; UDI #s (01)00884838059474(21)100783, (01)00884838059474(21)100848

Philips North America, LLC

FDA Devices Moderate May 13, 2020

Gentell Honey Hydrogel 4"x8" Saturated Gauze- A hydrating wound dressing containing hydrogel and honey (100% Leptospermum honey), Model Number: GEN-…

Gentell, Inc

FDA Devices Moderate May 13, 2020

REF: B90240-50, 96" (244 cm) Appx 11.2 ml, 10 Drop Admin Set w/Coiled Tubing, Pre-Slit Port, Clave, Rotating Luer, Sterile R, UDI: (01)00887709077058

ICU Medical, Inc.

FDA Devices Moderate May 13, 2020

BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Tubing: 110 in. (280 cm) - Blue Stripe - Product Usage: The system is intended for pa…

CME America, LLC

FDA Devices Moderate May 13, 2020

Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 C17/5 - ceramic for dental use, intended for IPS e.max ZirCAD presintered yttrium oxide-stabilized…

Ivoclar Vivadent AG

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175732P0 - Product Usage: for use in the replacement or repair o…

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

Siemens Aptio Automation Centrifuge Module, tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf an…

Inpeco S.A.

FDA Devices Moderate May 13, 2020

Universal Base CC RP 1.5 mm; The Universal Base Abutment in combination with Nobel Biocare end osseous implants are indicated for single-unit if scre…

Nobel Biocare Usa Llc

FDA Devices Moderate May 13, 2020

Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Product Usage: Probes are used for the fragmentation of urinary/renal and biliary calculi.

Northgate Technologies, Inc.

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175924P0 - Product Usage: for use in the replacement or repair o…

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal, Product Code: M00202175428T0 - Product Usage: for use in the replacement or …

Maquet Cardiovascular, LLC

FDA Devices Moderate May 13, 2020

REF: Z2850, 112" (284 cm) 10 Drop Primary set w/2 Clave, Remv 3 Gang 1o2 Manifold w/3 Clave, Baseplate, Rotating Luer w/Filter Cap, 1 Ext, Sterile R,…

ICU Medical, Inc.

FDA Devices Moderate May 13, 2020

da Vinci SP Instrument Arm Drape. REF 430013-12 QTY 1 Pouch

Intuitive Surgical, Inc.

FDA Devices Moderate May 13, 2020

daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm, REF 48360G-08, UDI: 00886874113844, Rx Only, Sterile EO - Product Usage: are intended to …

Intuitive Surgical, Inc.

FDA Devices Moderate May 13, 2020

Temporary Snap Abutment Engaging CC RP 1.5 mm; Pre-manufactured prosthetic components directly connected to the endosseous implant; catalog no. 38761…

Nobel Biocare Usa Llc

FDA Devices Moderate May 13, 2020

Transducer S8-3t UDI (01)00884838073524 REF 989605431171 Can be used as accessory with: EPIQ 7, Affiniti 70, EPIQ 5, EPIQ CVxi Ultrasound syst…

Philips Ultrasound Inc

FDA Devices Moderate May 13, 2020

Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only sold in the US. Drape/ UDI: HH2000/10858701006329; HH9006/ 10858701006282

Stryker Corporation

FDA Devices Low May 13, 2020

ARCHITECT C Peptide Calibrator - Product Usage: used as an aid in the diagnosis and treatment of patients with abnormal insulin secretion including d…

Abbott Laboratories

FDA Devices Moderate May 13, 2020

Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definition 120 Multileaf Collimator Model Number(s): prod…

Varian Medical Systems, Inc.

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175928P0 - Product Usage: for use in the replacement or repair …

Maquet Cardiovascular, LLC

FDA Devices Low May 13, 2020

ARCHITECT C Peptide Reagent - Product Usage: used as an aid in the diagnosis and treatment of patients with abnormal insulin secretion including diab…

Abbott Laboratories

FDA Devices Moderate May 13, 2020

3.5mm Aresenal Screw Drill Bit , Ref: 330-35-001, Qty. 70, Rx Only, Non-Sterile, UDI: (01)00812926029696 - Product Usage: A drill bit facilitates imp…

Trilliant Surgical, LLC

FDA Devices Moderate May 13, 2020

WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Product Usage: is intended to give a patient limited mobility by reducing pa…

Wright Medical Technology Inc

FDA Devices Moderate May 13, 2020

Chest Support for R82 Mustang, Model Numbers: 861810, 861820, 861830; and Rabbit Up, Model Numbers: 869810, 869820, 869830

R82 A/S

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175734P0 - Product Usage: for use in the replacement or repair …

Maquet Cardiovascular, LLC

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2020