PlainRecalls

2020 Recalls

5,998 recalls · Page 39 of 120

2020 Recall Year Insight

Federal agencies issued 5,998 product recalls indexed by PlainRecalls in calendar year 2020. That represents about 5.90% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 16.4 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 120 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 9 critical, 40 moderate, and 1 lower-severity recalls. The page references 25 distinct recalling firms operating in 6 distinct product categories, with 40 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (34), NHTSA (10), CPSC (6), 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 Sep 2, 2020

Datascope Intra-Aortic Balloon Catheters (IABs)-MEGA 7.5Fr 40cc IAB Kit P/N: 0684-00-0295-01, 0684-00-0295-01U, 0684-00-0295-02, 0684-00-0295-02U, 06…

Datascope Corporation

FDA Devices Moderate Sep 2, 2020

Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 30cc IAB (Japan) Kit P/N: 0684-00-0559-01 - Product Usage: Indications For Use: A…

Datascope Corporation

FDA Devices Moderate Sep 2, 2020

Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation Plus 7.5 Fr 40cc IAB Kit P/N: 0684-00-0568-01, 0684-00-0568-01U, 0684-00-0568-05, 0684-00-05…

Datascope Corporation

FDA Devices Moderate Sep 2, 2020

Klarity Vacuum Bags, Item Nos. R7504-30C, R7504-35BC,R7504-35C, R7644-32.5BC, RC7221-25BC, RC7504-17.5C - Product Usage: To be used by trained medica…

Klarity Medical Products LLC

FDA Devices Moderate Sep 2, 2020

Conformis iTotal Cruciate Retaining (CR) Knee Replacement System- Orthopedic Implant Cat: TCR-121-1111-010102, (ITOTAL CR IPOLY XE IMPLANT KIT LEFT)

Conformis, Inc.

FDA Devices Moderate Sep 2, 2020

Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 6.0mm REF NVTKIT-C6-5, Rx Only, Sterile, UDI: B006NVTKITC652/$$7061918A - Product Usage: …

Neurovision Medical Products Inc

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x31, 8-12mm, 8¿ (sterile)

Globus Medical, Inc.

FDA Devices Moderate Sep 2, 2020

Cios Alpha, Image-Intensified Fluoroscopic X-Ray System The Cios Alpha and Cios Spin are a mobile X-Ray system designed to provide X-ray imaging o…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 2, 2020

Cobra x5 1-Ch EMG ET Tube, 8.0mm, REF: LTE700L-5, Rx Only, Sterile EO UDI: B006LTE700L52$$7061318B - Product Usage: For continuous EMG monitoring a…

Neurovision Medical Products Inc

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x36, 9-13mm, 8¿

Globus Medical, Inc.

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x31, 10-14mm, 8¿

Globus Medical, Inc.

FDA Devices Moderate Sep 2, 2020

System Model: Ultimax-i, DREX-UI80 (DREX-UI80); Unit Model: HDR-08A Imager Processor; UDI (01)04987670100147

Canon Medical System, USA, INC.

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x36, 10-14mm, 8¿

Globus Medical, Inc.

FDA Devices Moderate Sep 2, 2020

Neurosign V4 Intraoperative Nerve monitor family of devices.

The Magstim Company Limited

FDA Devices Moderate Sep 2, 2020

Cobra x5 2-Ch EMG ET Tube, 6.0mm, REF: LTE700DCS-5, Rx Only, Sterile EO UDI: B006LTE700DCS52/$$7062618C - Product Usage: For continuous EMG monitor…

Neurovision Medical Products Inc

FDA Devices Moderate Sep 2, 2020

Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 40cc IAB (Japan) Kit P/N: 0684-00-0608 - Product Usage: Indications For Use: Acu…

Datascope Corporation

FDA Devices Moderate Sep 2, 2020

Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 40cc IAB Kit P/N: 0684-00-0470-01, 0684-00-0470-01U, 0684-00-0470-07, 0684-00-0470-09 - …

Datascope Corporation

FDA Devices Moderate Sep 2, 2020

VITROS Chemistry Products BuBc Slides - in vitro diagnostic use only. VITROS Chemistry Products BuBc Slides quantitatively measure unconjugated bilir…

Ortho-Clinical Diagnostics

FDA Devices Moderate Sep 2, 2020

Flexible Intubation Video Endoscope, Part: 11302BDX, with Instruction Manual: Z18443US - Product Usage: are intended to be used for examination and v…

Karl Storz Endoscopy

FDA Devices Low Sep 2, 2020

Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate Matrix Oral Fluid Coated Micro-Plate-IVD Immunoassay for Benzodiazepine…

OraSure Technologies, Inc.

FDA Devices Moderate Sep 2, 2020

Match Point System The Match Point System is intended to by uses as a surgical instrument to assist in the intraoperative positioning of glenoid c…

Materialise N.V.

FDA Devices Moderate Sep 2, 2020

Flexible DCI Intubation Fiberscope, Part: 11301BND1, with Instruction Manual: Z18445US - Product Usage: are intended to be used for examination and v…

Karl Storz Endoscopy

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x26, 9-13mm, 8¿

Globus Medical, Inc.

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x26, 10-14mm, 8¿

Globus Medical, Inc.

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x31, 10-14mm, 15¿

Globus Medical, Inc.

FDA Devices Moderate Sep 2, 2020

Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube, 7.0mm REF: NVTKIT-C7-5, RxOnly, Sterile, UDI: B006NvtKITc752/$$7062818C - Product Usage…

Neurovision Medical Products Inc

FDA Devices Moderate Sep 2, 2020

Flexible Intubation Video Endoscope, Part: 11301BNX, with Instruction Manual: Z18444US - Product Usage: are intended to be used for examination and v…

Karl Storz Endoscopy

FDA Devices Moderate Sep 2, 2020

CARESCAPE R860 Ventilator The CARESCAPE R860 ventilator is a microprocessor based, electronically controlled, pneumatically driven ventilator that…

GE Healthcare, LLC

FDA Devices Moderate Sep 2, 2020

Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit P/N: 0684-00-0480-01, 0684-00-0480-01U, 0684-00-0480-01C, 0684-00-0480-02, …

Datascope Corporation

FDA Devices Moderate Sep 2, 2020

Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 34cc IAB Kit, P/N: 0684-00-0469-01, 0684-00-0469-01C, 0684-00-0469-01U, 0684-00-0469-07…

Datascope Corporation

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x31, 12-16mm, 15¿

Globus Medical, Inc.

FDA Devices Moderate Sep 2, 2020

Cobra x5 2-Ch EMG ET Tube, 8.0mm, REF: LTE700DCL-5, Rx Only, Sterile EO UDI: B006LTE700DCL52 - Product Usage: For continuous EMG monitoring and sta…

Neurovision Medical Products Inc

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x26, 8-12mm, 8¿

Globus Medical, Inc.

FDA Devices Moderate Sep 2, 2020

ALTERA Spacer ALTERA Spacer, 10x26, 12-16mm, 15¿

Globus Medical, Inc.

CPSC Moderate Sep 2, 2020

Advantus Recalls Fluorescent Computer Task Lamps Due to Burn Hazard

CPSC Moderate Sep 2, 2020

Hanamint Recalls Swivel Rockers, Club Swivel Rockers and Club Swivel Gliders Due to Fall Hazard

CPSC Moderate Sep 2, 2020

IMMI Recalls Harnesses Made for Polaris, Can-Am, and Kawasaki UTVs Due to Injury Hazard

Indiana Mills & Manufacturing, Inc., of Westfield, Ind.

NHTSA Critical Sep 2, 2020

VOLVO 2020-2021: SERVICE BRAKES, AIR

VOLVO

NHTSA Critical Sep 2, 2020

VOLVO 2021: STEERING

VOLVO

NHTSA Moderate Sep 2, 2020

VOLKSWAGEN 2020: AIR BAGS:PASSENGER SIDE FRONTAL:CUSHION

VOLKSWAGEN

NHTSA Critical Sep 1, 2020

BMW 2020-2021: EXTERIOR LIGHTING:HEADLIGHTS

BMW

NHTSA Critical Sep 1, 2020

FREIGHTLINER 2020-2021: ENGINE AND ENGINE COOLING

FREIGHTLINER

CPSC Moderate Aug 27, 2020

Amazon Recalls Calmer Solutions Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Ale…

Calmer Solutions, of United Kingdom

CPSC Moderate Aug 27, 2020

Amazon Recalls Mystic Moments Birch Sweet Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

Mystic Moments UK, of United Kingdom

CPSC Moderate Aug 27, 2020

CPSC and Morpher Warn Consumers to Stop Using and Dispose of Bicycle Helmets Due to Risk of Head Injury; Recalling Firm is Unable to Conduct Recall (…

Strategic Sports Limited, of Hong Kong

NHTSA Critical Aug 27, 2020

HYUNDAI 2013-2015: SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE

HYUNDAI

NHTSA Critical Aug 27, 2020

KIA 2013-2015: SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE

KIA

NHTSA Critical Aug 27, 2020

KIA 2018-2021: SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE

KIA

NHTSA Critical Aug 27, 2020

LAND ROVER 2020: TIRES:PRESSURE MONITORING AND REGULATING SYSTEMS

LAND ROVER

NHTSA Critical Aug 27, 2020

BMW,TOYOTA 2019-2020: EXTERIOR LIGHTING:HEADLIGHTS

BMW,TOYOTA

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2020 across the FDA, CPSC and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.