PlainRecalls

2023 Recalls

Compiled from official public sources by the editorial team.

6,617 recalls · Page 11 of 133

2023 Recall Year Insight

Federal agencies issued 6,617 product recalls indexed by PlainRecalls in calendar year 2023. That represents about 6.51% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 18.1 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 133 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 2023.

On this page of 50 records, severity classification shows 9 critical, 38 moderate, and 3 lower-severity recalls. The page references 32 distinct recalling firms operating in 10 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (23), CPSC (12), FDA Drug (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 2023 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 Critical Dec 6, 2023

Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736…

Botanical Be

FDA Devices Moderate Dec 6, 2023

PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE

Aizu Olympus Co., Ltd.

FDA Devices Moderate Dec 6, 2023

Da Vinci Single-Site Wristed Needle Driver, REF: 478115, 5 mm

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 6, 2023

SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S

PATH

FDA Devices Moderate Dec 6, 2023

ICM LNQ22 LINQ II, Model LNQ22; Insertable Cardiac Monitor

Medtronic Inc.

FDA Devices Moderate Dec 6, 2023

with Notch 22M/15F sold as part of Breas Medical MPV circuit 2 pc Kits: 006093, 006653, an accessory to ventilator device, Vivo 45LS. intended …

Breas Medical, Inc.

FDA Devices Moderate Dec 6, 2023

Lugol s Iodine Solution 500ML, Part Number 624-71

EMD Millipore Corporation

FDA Devices Moderate Dec 6, 2023

RAPIDPOINT 500 Blood Gas System

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Dec 6, 2023

SENTIERO Screening2, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S2

PATH

FDA Devices Moderate Dec 6, 2023

SENTIERO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098

PATH

FDA Devices Moderate Dec 6, 2023

PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE

Aizu Olympus Co., Ltd.

FDA Devices Moderate Dec 6, 2023

CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE

Aizu Olympus Co., Ltd.

FDA Devices Moderate Dec 6, 2023

BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533

Becton Dickinson Infusion Therapy Systems Inc.

FDA Devices Moderate Dec 6, 2023

RAPIDPOINT 500e Blood Gas System

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Dec 6, 2023

GIF-H190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

Aizu Olympus Co., Ltd.

FDA Devices Moderate Dec 6, 2023

Acumen IQ Sensor with VAMP System, REFs: AIQS6AZ & AIQS6AZ5, STERILEEO, Rx only. For use in intravascular pressure monitoring.

Edwards Lifesciences, LLC

FDA Devices Moderate Dec 6, 2023

Alinity m HCV AMP kit, List (REF) Numbers: a) 08N50-095 and b) 08N50-090. The Alinity m HCV assay is an in vitro reverse transcription-polymerase ch…

Abbott Molecular, Inc.

FDA Devices Moderate Dec 6, 2023

TruWave Pressure monitoring set, REF: PX212: cc/12 in (30cm), PX260: (3 cc/60in (150cm), PX272: 3 cc/72in (180cm), PX284: 3 cc/84 in (210 cm), PX2X2:…

Edwards Lifesciences, LLC

FDA Devices Moderate Dec 6, 2023

FloTrac Sensor, REF: MHD8 & MHD85,MHD6R5, MHD8R, MHD8R5, MHD8S, STERILEEO, Rx only. For use in intravascular pressure monitoring.

Edwards Lifesciences, LLC

FDA Devices Moderate Dec 6, 2023

TruWave with Vamp System Pressure monitoring set, REF: PXAVMP(3cc)/VAMP 68 in (173cm) PXAVMP3: x3 (3cc)/VAMP PXVK0364:(3cc)/VAMP 96in (241cm); P…

Edwards Lifesciences, LLC

FDA Devices Moderate Dec 6, 2023

FloTrac Sensor with Vamp System, REF: MHD6AZ, MHD6AZ5 , MHD6C502 STIRLEEO, Rx only. For use in intravascular pressure monitoring.

Edwards Lifesciences, LLC

FDA Devices Moderate Dec 6, 2023

Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in intravascular pressure monitoring.

Edwards Lifesciences, LLC

FDA Devices Moderate Dec 6, 2023

GIF-HQ190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

Aizu Olympus Co., Ltd.

FDA Devices Moderate Dec 6, 2023

AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP

PATH

NHTSA Critical Dec 6, 2023

BMW,TOYOTA 2023: POWER TRAIN:AUTOMATIC TRANSMISSION:CONTROL MODULE (TCM/PCM/TECM)

BMW,TOYOTA

CPSC Moderate Dec 5, 2023

Foiresoft Zebra Roller Blinds Recalled Due to Strangulation and Entanglement Hazards; Sold Exclusively on Amazon.com by Softfunch (Recall Alert)

NHTSA Critical Dec 5, 2023

VOLVO 2024: EQUIPMENT:OTHER:LABELS

VOLVO

NHTSA Critical Dec 4, 2023

INFINITI 2022-2024: EXTERIOR LIGHTING:LIGHTING CONTROL MODULE

INFINITI

NHTSA Critical Dec 4, 2023

PORSCHE 2024: ELECTRICAL SYSTEM

PORSCHE

NHTSA Critical Dec 1, 2023

FREIGHTLINER,MERCEDES-BENZ 2021-2023: STRUCTURE:BODY

FREIGHTLINER,MERCEDES-BENZ

CPSC Moderate Nov 30, 2023

Berkshire Blanket & Home Company Recalls Heated Throws and Blankets Due to Fire and Thermal Burn Hazards

Berkshire Blanket & Home Co., of Ware, Massachusetts

CPSC Moderate Nov 30, 2023

GE Appliances, a Haier Company, Recalls Electric Cooktops Due to Burn Hazard

Haier US Appliance Solutions Inc., d/b/a GE Appliances, of Louisville, Kentucky

CPSC Moderate Nov 30, 2023

Klickpick Home Recalls Stainless Steel Children's Cup Sets Due to Violation of Federal Lead Content Ban; Sold Exclusively at Amazon.com (Recall Alert)

Shree Ashtavinayak LLC, dba Klickpick Home, of Throop, Pennsylvania

CPSC Moderate Nov 30, 2023

Pack and Play Mattresses Recalled Due to Suffocation Hazard for Infants; Violations to the Federal Safety Regulation for Crib Mattresses; Sold Exclus…

DODO Baby House, of China

CPSC Moderate Nov 30, 2023

Peg Perego Recalls Inclined Sleeper Bassinets for YPSI and Z4 Strollers Due to Risk of Suffocation and Fall Hazard; Violation of Federal Safety Stand…

Peg Perego SPA, of Italy

CPSC Moderate Nov 30, 2023

Polaris Recalls Patriot 850 MATRYX Snowmobiles Due to Injury Hazard (Recall Alert)

Polaris Industries Inc., of Medina, Minnesota

CPSC Moderate Nov 30, 2023

Polaris Recalls Patriot 9R MATRYX PRO RMK and Patriot 9R MATRYX RMK KHAOS Snowmobiles Due to Injury Hazard (Recall Alert)

Polaris Industries Inc., of Medina, Minnesota

CPSC Moderate Nov 30, 2023

Russound Recalls AW70V6 Loudspeakers Due to Impact Injury Injury Hazard

CPSC Moderate Nov 30, 2023

Specialized Bicycle Components Recalls Supacaz Brand Orbitron Pedals Due to Fall Hazard (Recall Alert)

CPSC Moderate Nov 30, 2023

Tiblue Stainless Steel Children's Cups Recalled Due to Violation of Federal Lead Content Ban; Sold Exclusively on Amazon.com by FENGM (Recall Alert)

FENGM (Hong Kong Fengmang International Co. Ltd.), of China

CPSC Moderate Nov 30, 2023

Vibe Bear Playyard Mattresses Recalled Due to Suffocation Hazards for Infants; Violation of the Federal Safety Regulation for Crib Mattresses; Sold E…

Beyond Baby, of China

FDA Food Low Nov 29, 2023

ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.

ActiPharma, Inc.

FDA Food Moderate Nov 29, 2023

Asenzya Hot & Spicy Cajun Style Seasoning, Item 121331. Net Wt 15 lbs. Distributed by: Asenzya 7616 South Sixth Street, Oak Creek, WI 53154.

Asenzya Inc.

FDA Food Moderate Nov 29, 2023

Jeni's Splendid Ice Cream: Buttercream Birthday Cake Ice Cream packaged in paperboard pint cups with heat seals and paper lids - 8 pints per case

Jeni's Splendid Ice Creams LLC

FDA Food Low Nov 29, 2023

HEB Central Market Blueberry Buckwheat Gluten Free Waffle, 8.25oz, UPC 004122025365 Giant Eagle Blueberry Gluten Free Waffle, 11.3oz, UPC 03003494494…

Treehouse Foods

FDA Drug Critical Nov 29, 2023

ELCYS (cysteine hydrochloride injection), USP, 500 mg/10mL (50 mg/mL), 10x10 mL Single Dose Sterile Vials, For Intravenous Infusion Only, Rx Only, Ma…

Exela Pharma Sciences LLC

FDA Drug Low Nov 29, 2023

Lisinopril Tablets USP 20 mg, packaged in a) 15-count blister card (NDC 0615-7718-05), b) 30-count blister card (NDC 0615-8255-39), Rx only, Mfd By L…

NCS Healthcare of Kentucky Inc

FDA Drug Critical Nov 29, 2023

LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottle, Sterile, Distributed By Cardin…

Cardinal Health Inc.

FDA Drug Critical Nov 29, 2023

LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), 0.5 FL OZ (15 mL) dropper bottles, …

Cardinal Health Inc.

FDA Drug Moderate Nov 29, 2023

Integrity Biochem HSC 70-VA, Alcohol Antiseptic 70%, Hand Sanitizer, Vanilla Scented Topical Gel 208.19L (55 gallons)- drum. Integrity Biochem, 1100…

Integrity Bio-Chemicals LLC

Nearby Recall Years

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

Compare 2023 with 2022 →

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 2023

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 2023 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.