PlainRecalls

2022 Recalls

5,888 recalls · Page 55 of 118

2022 Recall Year Insight

Federal agencies issued 5,888 product recalls indexed by PlainRecalls in calendar year 2022. That represents about 5.79% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 16.1 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 118 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 2022.

On this page of 50 records, severity classification shows 22 critical, 28 moderate, and 0 lower-severity recalls. The page references 30 distinct recalling firms operating in 4 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (32), NHTSA (8), FDA Food (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 2022 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 Jul 13, 2022

GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data within a computer network or on a…

GE Healthcare, LLC

FDA Devices Moderate Jul 13, 2022

VERIGENE Enteric Pathogens Nucleic Acid Test, Part No. 30-002-23

Luminex Corporation

FDA Devices Moderate Jul 13, 2022

Artis Icono, Interventional Fluoroscopic X-Ray System, Model No. 11327600

Siemens Medical Solutions USA, Inc

FDA Devices Critical Jul 13, 2022

Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.

Covidien Llc

FDA Devices Critical Jul 13, 2022

Palindrome Precision HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.

Covidien Llc

FDA Devices Moderate Jul 13, 2022

RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one MICS injection system with Intraocular Lens: (1) Outer carton labeled as…

Rayner Intraocular Lenses Ltd

FDA Devices Moderate Jul 13, 2022

Omnera 400A Digital Radiographic System

Arcoma AB

FDA Devices Critical Jul 13, 2022

Clean Catch Urine Kit NS 178489, AHMU58A

American Contract Systems, Inc.

FDA Devices Moderate Jul 13, 2022

Dimension LTNI -In vitro diagnostic test intended to quantitively measure cardiac troponin-I levels in human serum and heparinized plasma to aid in t…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Critical Jul 13, 2022

Nasopharyngeal sample collection tray for COVID-19 testing, labeled as COVID TEST KIT NONSTERILE 184312, AHCV18A

American Contract Systems, Inc.

FDA Devices Moderate Jul 13, 2022

Dimension CTNI-In vitro diagnostic test intended to quantitively measure cardiac troponin-I levels in human serum and heparinized plasma to aid in th…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Critical Jul 13, 2022

Palindrome H Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.

Covidien Llc

FDA Devices Moderate Jul 13, 2022

MassCheck Amino Acid, Acylcarnitines Dried Blood Spot Control Level I

Chromsystems Instruments & Chemicals GmbH

FDA Devices Critical Jul 13, 2022

Palindrome SI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.

Covidien Llc

FDA Devices Moderate Jul 13, 2022

Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 13, 2022

Omnera 400T Digital Radiographic System

Arcoma AB

FDA Devices Moderate Jul 13, 2022

CELLSEARCH Circulating Tumor Cell Kit (Epithelial)-IVD intended for the enumeration of circulating tumor cells (CTC) of epithelial origin (CD45-, EpC…

Menarini Silicon Biosystems

FDA Devices Critical Jul 13, 2022

Mahurkar Chronic Carbothane (Maxid) Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.

Covidien Llc

FDA Devices Moderate Jul 13, 2022

EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients…

DePuy Spine, Inc.

FDA Devices Moderate Jul 13, 2022

EEA Autosuture Circular Stapler with DST Series Technology, 25mm. Model Numbers EEA25, EEAXL25, EEA2535, and EEAXL2535.

Covidien, LP

FDA Devices Moderate Jul 13, 2022

Verigene CDF Nucleic Acid Test, Part No. 30-002-22

Luminex Corporation

FDA Devices Moderate Jul 13, 2022

OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis, sized for children and adolescents.

Ossur Americas

FDA Devices Moderate Jul 13, 2022

Abbott TactiCath Sensor Enabled, Contact Force Ablation Catheter, 8F 115cm FJ, REF A-TCSE-FJ. For mapping of the heart chambers during ablation.

Abbott

FDA Devices Critical Jul 13, 2022

Palindrome Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.

Covidien Llc

FDA Devices Moderate Jul 13, 2022

ABL800 Flex Analyzer Model Numbers 393-800 and 393-801

Radiometer Medical ApS

FDA Devices Critical Jul 13, 2022

Palindrome Precision H Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusio…

Covidien Llc

FDA Devices Critical Jul 13, 2022

Palindrome Precision SI Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusi…

Covidien Llc

FDA Devices Moderate Jul 13, 2022

NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal, Model No. 08-2301-3

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Jul 13, 2022

syngo Application software VE20 (Material Number 10848815) installed on the Artis pheno and Artis icono systems as follows: (1) Artis pheno Model …

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 13, 2022

MassCheck Amino Acid, Acylcarnitines Dried Blood Spot Control Level II

Chromsystems Instruments & Chemicals GmbH

FDA Devices Moderate Jul 13, 2022

EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients…

DePuy Spine, Inc.

FDA Devices Critical Jul 13, 2022

Palindrome HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.

Covidien Llc

NHTSA Critical Jul 13, 2022

TOYOTA 2022: ELECTRICAL SYSTEM:ADAS:PARKING ASSIST:SOFTWARE

TOYOTA

NHTSA Critical Jul 11, 2022

MERCEDES-BENZ 2020: POWER TRAIN:AUTOMATIC TRANSMISSION

MERCEDES-BENZ

NHTSA Critical Jul 11, 2022

MERCEDES-BENZ 2021: ELECTRICAL SYSTEM:WIRING

MERCEDES-BENZ

NHTSA Critical Jul 8, 2022

SUBARU 2020-2021: POWER TRAIN:AUTOMATIC TRANSMISSION:CONTROL MODULE (TCM/PCM/TECM)

SUBARU

NHTSA Critical Jul 8, 2022

MITSUBISHI 2022: BACK OVER PREVENTION:DISPLAY FUNCTION

MITSUBISHI

CPSC Moderate Jul 7, 2022

John Deere Recalls Lawn Tractors Due to Crash and Injury Hazards (Recall Alert)

Deere & Company, of Moline, Illinois

CPSC Moderate Jul 7, 2022

Samson International Recalls Cayden 9-Drawer Chests Due to Tip-Over and Entrapment Hazards; Sold Exclusively at Costco (Recall Alert)

Lacquer Craft Mfg. Co., Ltd of China, a subsidiary of Samson Holding Ltd.

CPSC Moderate Jul 7, 2022

Scholastic Recalls Shake Look Touch Books Due to Choking Hazard

CPSC Moderate Jul 7, 2022

Segway Powersports Recalls Fugleman Utility Terrain Vehicles (UTVs) Due to Fire Hazard (Recall Alert)

Segway Technology Co. Ltd., of China

NHTSA Critical Jul 7, 2022

FORD,LINCOLN 2020-2022: ENGINE AND ENGINE COOLING

FORD,LINCOLN

NHTSA Critical Jul 7, 2022

BMW 2022-2023: ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL

BMW

NHTSA Critical Jul 7, 2022

MERCEDES-BENZ 2016-2018: TIRES

MERCEDES-BENZ

FDA Food Critical Jul 6, 2022

PEANUT BUTTER CHOCOLATE FUDGE BITES (24-8 OZ) FUDGEAMENTALS

Fudgeamentals LLC

FDA Food Moderate Jul 6, 2022

PurAqua Belle Vie SPARKLING WATER wellness RELAX 100mg ASHWAGANDHA PER 12 FL OZ STRAWBERRY CUCUMBER FLAVORED SPARKLING WATER WITH OTHER NATURAL FLAVO…

Independent Beverage Company LLC

FDA Food Moderate Jul 6, 2022

The content inside package is walnut but was mis-labeled as Nutritional Yeast and packaged in a stand up plastic pouch. Net Weight: 0.6lb (272g). UPC…

Honey Heaven Wholesale Inc

FDA Food Critical Jul 6, 2022

VARIETY TRAY (16 OZ) (C-CNC-PBC) FUDGEAMENTALS

Fudgeamentals LLC

FDA Food Moderate Jul 6, 2022

Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 710-0-0627

Wilton Industries Inc

FDA Food Critical Jul 6, 2022

Quick Chek, #14294 Apples and Peanut Butter Snack Tray, each case is 12/ 5.1 oz. Plastic Tray with lid, 12 packages per case, Keep refrigerated.

Safeway Fresh Foods LLC

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2022 with 2021 →

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 2022

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 2022 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.