PlainRecalls

2022 Recalls

Compiled from official public sources by the editorial team.

5,888 recalls · Page 2 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 11 critical, 38 moderate, and 1 lower-severity recalls. The page references 23 distinct recalling firms operating in 9 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (29), FDA Drug (9), 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 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 Dec 28, 2022

X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.

NuVasive Inc

FDA Devices Moderate Dec 28, 2022

B125P Patient Monitor (with E-module slot option), REF 6160000-002

GE Medical Systems, LLC

FDA Devices Moderate Dec 28, 2022

HeartWare HVAD Pump Kit, REF MCS1705PU

Heartware, Inc.

FDA Devices Moderate Dec 28, 2022

B105M Patient Monitor, REF 6160000-003

GE Medical Systems, LLC

FDA Devices Moderate Dec 28, 2022

Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-090

Abbott Molecular, Inc.

FDA Devices Moderate Dec 28, 2022

Revaclear 400 Dialyzer. Product Code: 114749M. Not distributed in the USA. Used to treat chronic and acute renal failure by hemodialysis.

Baxter Healthcare Corporation

FDA Devices Moderate Dec 28, 2022

HeartWare Model 1102

Heartware, Inc.

FDA Devices Moderate Dec 28, 2022

InPen Diabetes Management App, part of the InPen System, REF: MMT-105ELBLNA, MMT-105ELGYNA, MMT-105ELPKNA, MMT-105ELPKNA, MMT-105NNBLNA, MMT-105NNGYN…

Companion Medical, Inc.

FDA Devices Moderate Dec 28, 2022

Vivid S6 N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ…

GE Medical Systems, LLC

FDA Devices Moderate Dec 28, 2022

HeartWare HVAD Pump Kit, REF 1205

Heartware, Inc.

FDA Devices Moderate Dec 28, 2022

HeartWare HVAD Pump Kit, REF 1104JP

Heartware, Inc.

FDA Devices Moderate Dec 28, 2022

Vivid i N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ …

GE Medical Systems, LLC

FDA Devices Moderate Dec 28, 2022

B125M Patient Monitor, REF 6160000-005-XXXXXXX

GE Medical Systems, LLC

FDA Devices Moderate Dec 28, 2022

The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set that is used to create an intr…

Natus Medical Incorporated

FDA Devices Moderate Dec 28, 2022

Centricity PACS-IW with Universal Viewer version 5.0. Used to display medical images (Including mammograms) and data from various imaging source…

GE Medical Systems, LLC

FDA Devices Moderate Dec 28, 2022

Revaclear 400 Dialyzer. Product Code: 114746L. Used to treat chronic and acute renal failure by hemodialysis.

Baxter Healthcare Corporation

FDA Devices Moderate Dec 28, 2022

Revaclear 400 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.

Baxter Healthcare Corporation

NHTSA Critical Dec 23, 2022

MERCEDES-BENZ 2013-2020: FUEL SYSTEM, DIESEL:DELIVERY:FUEL PUMP:CONTROL/DRIVE MODULE

MERCEDES-BENZ

NHTSA Critical Dec 23, 2022

MERCEDES-BENZ 2002-2011: VISIBILITY:SUN/MOON ROOF ASSEMBLY

MERCEDES-BENZ

NHTSA Critical Dec 23, 2022

LINCOLN 2020-2023: SEAT BELTS:FRONT:WARNING LIGHT/DEVICES

LINCOLN

CPSC Moderate Dec 22, 2022

BLU3 Recalls Nomad Battery-Powered Tankless Diving Systems Due to Drowning Hazard for Divers

BLU3, of Pompano Beach, Florida

CPSC Moderate Dec 22, 2022

KTM North America Recalls GASGAS Off-Road Motorcycles Due to Crash and Injury Hazards

CPSC Moderate Dec 22, 2022

Nova Medical Products Recalls Adult Bed Rails Due to Serious Entrapment and Asphyxia Hazards

Bliss Health Products Co. Ltd., of China

CPSC Moderate Dec 22, 2022

Pacific Cycle Recalls Pacific Kids' Igniter and Pacific Bubble Pop 20-Inch Bicycles Due to Fall Hazard; Sold Exclusively at Target

CPSC Moderate Dec 22, 2022

Samsung Recalls Top-Load Washing Machines Due to Fire Hazard; Software Repair Available

Samsung Electronics America Inc., of Ridgefield Park, New Jersey

CPSC Moderate Dec 22, 2022

Target Recalls Children's Pillowfort Weighted Blankets Due to Asphyxiation Hazard; Two Fatalities Reported

NHTSA Critical Dec 22, 2022

ACURA 2022: TIRES:BEAD

ACURA

NHTSA Critical Dec 22, 2022

RAM 2022: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

RAM

FDA Food Moderate Dec 21, 2022

Sardines in tomato sauce packed in cans labeled in part, "WILD PACIFIC SARDINES RAINCOAST TRADING TM***IN TOMATO SAUCE***NET. 4.2 oz (120 g)***INGRED…

St. Jean's Coast Mountain Resources Ltd. (dba) St. Jean's Ca

FDA Drug Moderate Dec 21, 2022

ProSirona, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Dist. by: Endometriosis Assoc. Inc. (International), Mfg. by…

Atlantic Management Resources Ltd.

FDA Drug Moderate Dec 21, 2022

FentaNYL Citrate 2.5 mg/50 mL (50mcg/ml) Injection Solution, Preservative Free, Single Use 50 ml Cassette, Rx Only, Repackaged by OurPharma, LLC. 251…

OurPharma LLC

FDA Drug Low Dec 21, 2022

Lacosamide Oral Solution, USP, CV, 10mg/mL, packaged in 200 mL bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854,…

Camber Pharmaceuticals, Inc

FDA Drug Critical Dec 21, 2022

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, In…

Exela Pharma Sciences LLC

FDA Drug Moderate Dec 21, 2022

Neuroquell Plus, Advanced Formula, A Homeopathic Drug, Calendula Oil packaged in 0.22 Fl. oz. (6.6 mL) bottles, Mfg. for/Dist. By Claire Ellen Topica…

Atlantic Management Resources Ltd.

FDA Drug Critical Dec 21, 2022

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx only, Manufactured and Di…

Exela Pharma Sciences LLC

FDA Drug Moderate Dec 21, 2022

Menastil, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westbor…

Atlantic Management Resources Ltd.

FDA Drug Critical Dec 21, 2022

Iohexol (300 mg Iodine/mL), 2.4 g Iodine/8 ml, Total Volume 8 ml in 10 ml syringe, 5-count syringes packaged in a bag labeled as Omnipaque (iohexol) …

BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy

FDA Drug Moderate Dec 21, 2022

Neuroquell, A Homeopathic Drug, Calendula Oil, packaged in1/8 Fl. oz. (3.5 g) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westboro…

Atlantic Management Resources Ltd.

FDA Devices Moderate Dec 21, 2022

HENRY SCHEIN, Vas Reversal Pack, Item No.888-2549,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal MYELOGRAM PACK, REF 89-9304.05

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal LUMBAR/CERVICAL PACK, REF 89-9521.11

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Angioplasty, Item No.682-1937,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal VIT RD PACK 86ST, REF 89-7308.09

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT2 WAVE REFURBISHED, REF IAP-0535X (IPN000329), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Surg Pk, Item No.40714IES, oral surgery tray

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-05001 (IPN000333), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT 2 WAVE, REF IAP-0535 (IPN000329), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal FOOT PACK, REF 89-9252.08

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal PAIN TRAY, REF 89-10464.03

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

HENRY SCHEIN, SINGLE SHOT EPIDURAL, Item No.570-3089

Stradis Medical, LLC dba Stradis Healthcare

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.