PlainRecalls

2020 Recalls

5,939 recalls · Page 86 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 2 critical, 48 moderate, and 0 lower-severity recalls. The page references 23 distinct recalling firms operating in 3 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (41), FDA Drug (9), 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 Mar 25, 2020

Solifenacin Succinate Tablets, 10 mg, packaged in a) 30-count bottles (NDC 51991-894-33) and b) 90-count bottles (NDC 51991-894-90), Distributed by:…

Breckenridge Pharmaceutical, Inc

FDA Drug Moderate Mar 25, 2020

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 8 tablets. [NDC: Brand] NDC Good Sense:0113-0852-51; NDC Walgreens 0363-0852-51

Perrigo Company PLC

FDA Drug Moderate Mar 25, 2020

Solifenacin Succinate Tablets, 5mg, packaged in a) 30-count bottles (NDC 51991-893-33) and b) 90-count bottles (NDC 51991-893-90) Distributed by: Bre…

Breckenridge Pharmaceutical, Inc

FDA Drug Critical Mar 25, 2020

UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack, c) ten pack capsules per carton, Exclusively Manufactured and…

Med Man Distribution, Inc.

FDA Drug Moderate Mar 25, 2020

Daytrana (methylphenidate transdermal system) patches, Delivers 15 mg over 9 hours (1.6 mg/hr), 30-count box, Rx only, Manufactured for Noven Therape…

Noven Therapeutics, LLC

FDA Drug Moderate Mar 25, 2020

Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 90 tablets per bottle. [Brand, NDC] NDC Equate: 49035-800-75; NDC Up & Up: 1…

Perrigo Company PLC

FDA Drug Moderate Mar 25, 2020

Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 60 tablets per bottle. [NDC: Brand] NDC Health Mart: 62011-0283-2; NDC Major: 0904-6715…

Perrigo Company PLC

FDA Drug Moderate Mar 25, 2020

Atorvastatin Calcium Tablets, USP 40 mg, Rx only, 500-count bottle, Manufactured by: Sun Pharmaceutical Industries Limited Mohali, INDIA, Distributed…

Sun Pharmaceutical Industries, Inc.

FDA Drug Moderate Mar 25, 2020

Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg, 90 count bottle, Rx Only, Manufactured by Jubilant Generics Ltd, Roorkee-247661 India, NDC 5…

Jubilant Cadista Pharmaceuticals, Inc.

FDA Devices Moderate Mar 25, 2020

Integris Allura 9, system codes 722018 722021

Philips North America, LLC

FDA Devices Moderate Mar 25, 2020

Cardio Vascular-Allura Centron, system code 722400

Philips North America, LLC

FDA Devices Moderate Mar 25, 2020

Medtronic CareLink 2090 Programmer. Used to interrogate and program Medtronic and Vitatron implantable devices, such as pacemaker/ICD/CRT.

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA Devices Moderate Mar 25, 2020

Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multip…

Avid Medical, Inc.

FDA Devices Moderate Mar 25, 2020

IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 tests) and L2KE26(D) (600 tests) and OUS: L2KE22 (200 tests), L2KE26 (600 tests) - P…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Mar 25, 2020

AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Product Usage: TomoSynthesis is used to synthesize tom…

Agfa N.V.

FDA Devices Moderate Mar 25, 2020

OsteoSelect Demineralized Bone Matrix (DBM) Putty 10.0cc in a syringe; STERILE R, Product Code: 359100, Dimensions: ONE(1) PACKAGE - CONTAINING 10.0c…

XTANT MEDICAL INC

FDA Devices Moderate Mar 25, 2020

Artis Q.zen Biplane, Model No. 10848355 Artis Q.zen Ceiling, Model No. 10848354 Artis Q.zen Floor, Model No. 10848353 Product Usage: Artis is a fa…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Mar 25, 2020

LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T System is used to circulate water through heat exchangers to warm or cool a pa…

LivaNova USA Inc.

FDA Devices Moderate Mar 25, 2020

Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multip…

Avid Medical, Inc.

FDA Devices Moderate Mar 25, 2020

UroDiagnost Eleva, system code 708033

Philips North America, LLC

FDA Devices Moderate Mar 25, 2020

TRUMATCH Orthognathic - Full Bimaxillary Surgical Kit, Catalog Number SD980.001

Materialise N.V.

FDA Devices Moderate Mar 25, 2020

Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multip…

Avid Medical, Inc.

FDA Devices Moderate Mar 25, 2020

Columbus R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN058K NN070K NN071K NN072K NN073K NN074K NN075K NN076K…

Aesculap Implant Systems LLC

FDA Devices Moderate Mar 25, 2020

D-0014 3COR 14MM DISTRACTION SCREWS, 5/BOX, STERILE - Product Usage: The 3COR Distraction Screws and the TSI Quick Start Distraction Screws products …

TeDan Surgical Innovations LLC

FDA Devices Moderate Mar 25, 2020

Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multip…

Avid Medical, Inc.

FDA Devices Moderate Mar 25, 2020

Artis Q Biplane, Model No. 10848282; Artis Q Ceiling, Model No.10848281; Artis Q Floor, Model No. 10848280; Artis Q zeego, Model No. 10848283 Pro…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Mar 25, 2020

COLUMBUS CRA/PSA TIB.PLAT.CEMENTED, Knee implant components, various sizes, model nos. NN469K NN470K NN471K NN472K NN473K NN474K NN475K NN476…

Aesculap Implant Systems LLC

FDA Devices Moderate Mar 25, 2020

COLUMBUS CR/PS TIB.PLAT.PLASMAPORE, Knee implant components, various sizes, model nos. NN081K NN082K NN083K NN084K NN085K NN086K NN087K NN088…

Aesculap Implant Systems LLC

FDA Devices Moderate Mar 25, 2020

OmniDiagnost Eleva System codes 708028 708027

Philips North America, LLC

FDA Devices Moderate Mar 25, 2020

Boston Scientific, LATITUDE Programming System, Model 3300 - Product Usage:The Boston Scientific LATITUDE Programming System is intended for use in h…

Boston Scientific Corporation

FDA Devices Moderate Mar 25, 2020

Teleflex Pilling Aortic Punch, 4.0mm. Sterile, Rx Only, disposable. Included as part of Intl-Cardiac Surgery Kit - Product Usage: This device is use…

Deroyal Industries, Inc. Lafollette

FDA Devices Moderate Mar 25, 2020

IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use with the IMMULITE systems Ana…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Mar 25, 2020

Ysio, model no. 10281013 Product Usage: The product is a stationary X-Ray system.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Mar 25, 2020

Stryker, REF: 0250070450, 5.0 mm x 45 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Sterile, CE, UDI: (01) 07613327051926 This products …

Stryker Corporation

FDA Devices Moderate Mar 25, 2020

Integris Allura 15 & 12, monoplane (system code 722043) and biplane (system code 722044)

Philips North America, LLC

FDA Devices Critical Mar 25, 2020

CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and CMExpress

CME America, LLC

FDA Devices Moderate Mar 25, 2020

Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multip…

Avid Medical, Inc.

FDA Devices Moderate Mar 25, 2020

HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M35…

Philips North America, LLC

FDA Devices Moderate Mar 25, 2020

Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multip…

Avid Medical, Inc.

FDA Devices Moderate Mar 25, 2020

MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038

Philips North America, LLC

FDA Devices Moderate Mar 25, 2020

Poly G Integris H5000, System code 72246

Philips North America, LLC

FDA Devices Moderate Mar 25, 2020

DS-0022 QUICK START DISTRACTION SCREW 12MM 5/BOX STERILE - Product Usage: These products are intended to be used by trained surgeons and are designed…

TeDan Surgical Innovations LLC

FDA Devices Moderate Mar 25, 2020

Rheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vitro diagnostic use, Product code: LK151.S.A. , UDI: 05051700018319

The Binding Site Group, Ltd.

FDA Devices Moderate Mar 25, 2020

TRUMATCH Orthognathics - Genioplasty Surgical Kit, Add-on, Catalog Number: SD980.013

Materialise N.V.

FDA Devices Moderate Mar 25, 2020

Low Profile Screw, 4.5 x 20 mm The Low Profile ScrewTM, 4.5 x 20 mm, AR-8545-20, is used with the Ankle Fusion Line of plates and is intended to p…

Arthrex, Inc.

FDA Devices Moderate Mar 25, 2020

AS COLUMBUS CR/PS TIB.PLAT.CEMENTED,Knee implant components, various sizes, model nos. NN058Z NN070Z NN071Z NN072Z NN073Z NN074Z NN075Z NN07…

Aesculap Implant Systems LLC

FDA Devices Moderate Mar 25, 2020

D-0012 3COR 12MM DISTRACTION SCREWS, 5/BOX, STERILE - Product Usage: The 3COR Distraction Screws and the TSI Quick Start Distraction Screws products …

TeDan Surgical Innovations LLC

FDA Devices Moderate Mar 25, 2020

COLUMBUS REV F TIBIA OFFSET CEMENTED, Knee implant components, various sizes, model nos. NR068K NR068Z NR070K NR070Z NR071K NR071Z NR072K NR0…

Aesculap Implant Systems LLC

FDA Devices Moderate Mar 25, 2020

Medtronic CareLink Encore 29901 Programmer. Used to interrogate and program Medtronic and Vitatron implantable devices, such as pacemaker/ICD/CRT.

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA Devices Moderate Mar 25, 2020

Boston Scientific, Implantable Cardioverter Defibrillator, DYNAGEN EL ICD DR, Model D152 - Product Usage: Implantable cardioverter defibrillators (IC…

Boston Scientific Corporation

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