PlainRecalls

2022 Recalls

5,806 recalls · Page 115 of 117

2022 Recall Year Insight

Federal agencies issued 5,806 product recalls indexed by PlainRecalls in calendar year 2022. That represents about 6.92% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 15.9 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 117 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 3 critical, 46 moderate, and 1 lower-severity recalls. The page references 29 distinct recalling firms operating in 7 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Drug (20), FDA Devices (18), CPSC (8), 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 Drug Moderate Jan 12, 2022

CAREONE Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, packaged as a)30 count bottle, NDC 41520-229-39, UPC 3 41520…

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

amazon, Allergy Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24 HR, 30 count bottle, Made in the Czech Republic, Distributed by: Amazo…

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

Wal-Fex Fexofenadine Hydrochloride tablets, 180mg/antihistamine, 24HR, packaged as a) 5 count bottle, NDC 0363-0600-13,UPC 3 11917 12267 0, b)30 co…

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

DG/health Aller.Ease, Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24HR, 10 count bottle, Distributed by: Made in Czech Republic. Dist…

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

Health Mart, Fexofenadine Hydrochloride tablets, 12HR, 60mg . Antihistamine 12 count bottle, Distributed by: Mckesson 6555 State Highway 161, Irv…

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

allergyrelief, Fexofenadine Hydrochloride tablets, 24HR, 1800mg Antihistamine, packaged as a) 15 count bottle, NDC 56062-571-22 UPC 0 41415 38973 1; …

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, packaged as a) 30 count bottle, NDC 11822-0571-2 UPC 0 11822 …

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

KIRKLAND ALLER-FEX, Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24HR, 180 count bottle, Made in the Czech Republic, Packaged by Perrig…

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

GoodSense Aller.Ease, Fexofenadine hydrochloride 24 HR, 180 mg tablets, 30 count bottle, Made in the Czech Republic, Distributed by Perrigo Allergan …

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

Perrigo Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, 100 count bottle, Made in the Czech Republic, Distributed by Perrigo Allerga…

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

berkley jensen, ALLERGY RELIEF, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, 150 count bottle, Made in the Czech Republic, Distri…

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

Pregabalin Capsules, 50 mg, 100 count bottle, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun …

SUN PHARMACEUTICAL INDUSTRIES INC

FDA Drug Moderate Jan 12, 2022

CVS Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, 30 count bottle, NDC 69842-698-39, UPC 0 50428 62564 4

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

MAJOR, Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 100 count bottle, Distributed by Major Pharmaceuticals 17177 N Laurel Park Dri…

Perrigo Company PLC

FDA Drug Moderate Jan 12, 2022

PAIN AID ESF- (Acetaminopehn USP 250mg, Asprin USP 250mg Caffeine 65mg) coated, bulk OTC tablets packaged in corrugated boxes lined with 2 polyethyle…

ULTRAtab Laboratories, Inc.

FDA Devices Moderate Jan 12, 2022

QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA EUA 200075); REF 691223

Qiagen Sciences LLC

FDA Devices Moderate Jan 12, 2022

Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: IFX-20R, IFX-20SP, IF…

Invacare Corporation

FDA Devices Moderate Jan 12, 2022

DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile

Medshape, INC.

FDA Devices Moderate Jan 12, 2022

DBB-06 Hemodialysis Delivery System

Nikkiso Ltd - Shizuoka Plant

FDA Devices Moderate Jan 12, 2022

UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.

Uromedica Inc.

FDA Devices Moderate Jan 12, 2022

Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for sterilization of re-usable instrument…

Howmedica Osteonics Corp.

FDA Devices Moderate Jan 12, 2022

Biomeme SARS-CoV-2- Real Time RT-PCR Test, Instructions for Use, Part number 100002824 Subcomponent of: SARS-CoV-2 Go-Strips, 3000555; SARS-CoV-2 Go…

Biomeme, Inc.

FDA Devices Moderate Jan 12, 2022

Alinity m System, Part No. 08N53-002

Abbott Molecular, Inc.

FDA Devices Low Jan 12, 2022

iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery System, Extra Strength, 8-HOUR Average Wear Time, 6/1-patch pouches/box.…

Tapemark Company

FDA Devices Moderate Jan 12, 2022

Alinity m System, Part No. 08N53-002

Abbott Molecular, Inc.

FDA Devices Moderate Jan 12, 2022

Alinity m System, Part No. 08N53-002

Abbott Molecular, Inc.

FDA Devices Moderate Jan 12, 2022

Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: TDX SP2: TDXSP2, TDXSP2…

Invacare Corporation

FDA Devices Moderate Jan 12, 2022

Alinity m System, Part No. 08N53-002

Abbott Molecular, Inc.

FDA Devices Moderate Jan 12, 2022

Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: SRX-20R, SRX-20S…

Invacare Corporation

FDA Devices Moderate Jan 12, 2022

Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue Ratchet Handle in order to fac…

Flower Orthopedics Corporation

FDA Devices Moderate Jan 12, 2022

Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An automated, clinical chemistry analyzer designed to perform in vitro diagnostic …

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jan 12, 2022

Instructions for Use for all model numbers of the Medtronic Abre Venous Self-Expanding Stent System.

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

FDA Devices Moderate Jan 12, 2022

Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455

DiaSorin Molecular LLC

CPSC Moderate Jan 12, 2022

Children's Robes Recalled by HulovoX Due to Violation of Federal Flammability Standards and Burn Hazard

HulovoX, of Zhejiang in China

CPSC Moderate Jan 12, 2022

EGL Motor Recalls Youth All-Terrain Vehicles (ATVs) Due to Injury Hazard and Violation of Federal ATV Safety Standard

Yongkang Jiayue Industry & Trading Co., Ltd., of China (model D110)

CPSC Moderate Jan 12, 2022

Giant Bicycle Recalls Bicycles Due to Fall and Injury Hazards

CPSC Moderate Jan 11, 2022

Bella Elevator Recalls Residential Elevators Due to Child Entrapment Hazard; Risk of Serious Injury or Death to Young Children

Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill.

CPSC Moderate Jan 11, 2022

Inclinator Company of America Recalls Residential Elevators Due to Child Entrapment Hazard; Risk of Serious Injury or Death to Young Children

Inclinator Company of America Inc., of Harrisburg, Pa.

CPSC Moderate Jan 11, 2022

Residential Elevators Recalled by Savaria Corporation Due to Child Entrapment Hazard; Risk of Serious Injury or Death to Young Children

Savaria Corporation, of Canada

CPSC Moderate Jan 6, 2022

Colony Brands Recalls Children's Wood Wagons Due to Violation of Federal Lead Paint Ban and Lead Poisoning Hazard (Recall Alert)

CPSC Moderate Jan 6, 2022

Polaris Recalls Youth All-Terrain Vehicles Due to Fire Hazard (Recall Alert)

FDA Food Moderate Jan 5, 2022

Tuna, raw sold at meat counter and wrapped in butcher paper at point of purchase.

Sant' Elia Operations, LLC

FDA Food Moderate Jan 5, 2022

Giant Eagle, Diced Green Peppers, 10 oz. poly bags and 22# cases, also poly bags and cartons, 12/10 oz. bags per case and bulk 22 lbs. bags

Frozen Food Development

FDA Food Moderate Jan 5, 2022

Giant Eagle Diced Green Peppers, 10 oz. 283 g, Frozen bag, 12 packages per case , Best By 10/14/2023 .

Giant Eagle, Inc.

FDA Food Critical Jan 5, 2022

BUBS Naturals Fountain of Youth Formula; Collagen Protein; Support for Hair, Skin & Nails; Biotin, Antioxidant, Vitamin C; Maqui Berry Net Wt. 10.16 …

Slayer Forever, LLC dba BUBS Naturals

FDA Drug Critical Jan 5, 2022

Klean Touch Hand Sanitizer (Ethyl Alcohol 70%) Ingredients Ethanol and Methanol, in 55-gallon drums, Aroma Release Technology, Inc., 7026 Discovery D…

Aroma Release Technologies Inc

FDA Drug Critical Jan 5, 2022

kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles, Distributed by: Valisa MFG, LLC, Farmingdale, NY, 11735, Made in USA…

Valisa MFG LLC

FDA Drug Moderate Jan 5, 2022

MORPHINE SULFATE, in 0.9% Sodium Chloride Injection, 50 mg per 50 mL, (1 mg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 7032…

SterRx, LLC

FDA Drug Moderate Jan 5, 2022

Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC 52565-023-29

Teligent Pharma, Inc.

FDA Drug Moderate Jan 5, 2022

NOREPINEPHRINE, 16 mg per 250 mL, (64 mcg per mL) in 5% Dextrose Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-002-01.

SterRx, 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