PlainRecalls

2023 Recalls

6,617 recalls · Page 110 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 8 critical, 40 moderate, and 2 lower-severity recalls. The page references 25 distinct recalling firms operating in 4 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (31), FDA Drug (16), NHTSA (3), 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 Mar 15, 2023

Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034 91379 9; Manu…

Pharmedica USA, LLC

FDA Drug Moderate Mar 15, 2023

NaturalCare bioAllers, Allergy Nasal Spray, Homeopathic, All Region Formula, 0.8 fl oz( 24mL), Mfd. Nutraceutical Corp., NaturalCare Park City, UT, 8…

Nutraceutical Corporation

FDA Drug Moderate Mar 15, 2023

Activator Concentrate (sodium fluoride 0.96% in Activator) 1 fl. Oz, liquid oral rinse plastic bottles, Manufactured for: All USA Direct LLC, Broadvi…

Ecometics, Inc.

FDA Drug Moderate Mar 15, 2023

NatraBio, Cold& Sinus Nasal Spray, Homeopathic Medicine, 0.8 FL Oz. ( 24ml), Mfd. for Healthway Corp. Comments or Questions NatraBio Shelburne Falls,…

Nutraceutical Corporation

FDA Drug Moderate Mar 15, 2023

Heparin Sodium Injection, USP, 20,000 USP units per mL, 25 x 1 mL Multi-Dose Vials, Rx Only, For Intravenous or Subcutaneous Use, Mfd. for: Sagent Ph…

Sagent Pharmaceuticals Inc

FDA Drug Moderate Mar 15, 2023

Metformin hydrochloride Extended-Release Tablets, 1000 mg, 60-count bottle, RX only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale,…

Teva Pharmaceuticals USA Inc

FDA Drug Moderate Mar 15, 2023

Vencedor medicated balm (capsaicin 0.028%) 1.5 oz. (43g) tubes, Distributed by: The Larkspur Group Inc. Norwalk, CT 06854

Ecometics, Inc.

FDA Drug Moderate Mar 15, 2023

Unguentine Original Ointment for Burns (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%) packaged in 1 oz. (28g) metal tubes, Distributed by:…

Ecometics, Inc.

FDA Drug Moderate Mar 15, 2023

Purely Soothing MSM Nasal Spray, 15%, packaged in 30ml, 1.014 fl. oz bottles, Manufactured by: Pharmedica USA, Phoenix, AZ, UPC 7 31034 91380 5

Pharmedica USA, LLC

FDA Drug Moderate Mar 15, 2023

Phenylephrine HCl 1mg per 10mL (100 mcg/mL) 10 mL syringes, Rx only, Leiters 13796 Compark Blvd Englewood CO 80112, NDC 71449-001-15

Denver Solutions, LLC DBA Leiters Health

FDA Drug Moderate Mar 15, 2023

Soltice Quick-RUB (Menthol 5.1%, Camphor 5.1%) packaged in a) 1.33 oz (37g) plastic jars and b) 3 Oz (85g) plastic jars

Ecometics, Inc.

FDA Drug Moderate Mar 15, 2023

Phenylephrine HCl 20 mg (80 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV Bag, Rx only, Leiters Compounding Health 13796 Compark Blvd Englewood CO …

Denver Solutions, LLC DBA Leiters Health

FDA Drug Moderate Mar 15, 2023

NaturalCare, children's, Allergy Care, Homeopathic, 4 Months and Up, Liquid Drops, 0.1% Alcohol, 1 FL OZ( 30mL), Mfd. Nutraceutical Corp., Salt Lake …

Nutraceutical Corporation

FDA Drug Low Mar 15, 2023

DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1

Akron Pharma, Inc.

FDA Drug Moderate Mar 15, 2023

Nose Better Gel (0.75% Camphor, 0.50% Menthol, 0.50% Allantoin), packaged in 0.46 oz. (13g) metal tubes, Distributed by: Oakhurst Company Levittown,…

Ecometics, Inc.

FDA Drug Moderate Mar 15, 2023

Verapamil Hydrochloride Extended-Release Tablets, USP, 120 mg, Rx Only, 100 Tablets per Carton (10 x 10), Distributed by: American Health Packaging, …

Amerisource Health Services LLC

FDA Devices Moderate Mar 15, 2023

Sensus Healthcare Inc, SRT-100 Vision IPX 0, HFUS Module IPX 1, with software version 1.9.2; Superficial X-ray Radiation Therapy System with Ultrason…

Sensus Healthcare, Inc.

FDA Devices Moderate Mar 15, 2023

CardioMEMS HF System PA Sensor and Delivery System, Model Number CM3100, The CardioMEMS HF System provides pulmonary artery (PA) hemodynamic data use…

St. Jude Medical

FDA Devices Moderate Mar 15, 2023

Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-75, 0998-00-0800-83, and 0998-00-0800-85

Datascope Corp.

FDA Devices Moderate Mar 15, 2023

CardioMEMS HF System PA Sensor and Delivery System, Model Number CM2000, The CardioMEMS HF System provides pulmonary artery (PA) hemodynamic data use…

St. Jude Medical

FDA Devices Low Mar 15, 2023

PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.

Preat Corp

FDA Devices Moderate Mar 15, 2023

Cardiosave Hybrid Intra-Aortic Balloon Pump. Model Numbers: D998-00-0800-31, D998-00-0800-32, D998-00-0800-33, D998-00-0800-35, D998-00-0800-36, D998…

Datascope Corp.

FDA Devices Moderate Mar 15, 2023

Heartsine Samaritan PAD: SAM 350P semi-automatic defibrillator, SAM 360P fully automatic defibrillator, SAM 500P semi-automatic defibrillator with …

HeartSine Technologies Ltd

FDA Devices Moderate Mar 15, 2023

Cardiosave Rescue. Model Number: 0998-00-0800-83.

Datascope Corp.

FDA Devices Critical Mar 15, 2023

Cardiosave Hybrid Model Nos. 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0998-00-0800-34 0998-00-0800-35 0998-00-0800-45 0998-00-0800-52…

Datascope Corp.

FDA Devices Moderate Mar 15, 2023

LetsGetChecked Blood Sample Collection kit-In vitro diagnostic medical device specifically intended for the primary containment and preservation of b…

LetsGetChecked Inc.

FDA Devices Moderate Mar 15, 2023

Monaco RTP System. Used to make treatment plans for patients with prescriptions for external beam radiation therapy.

Elekta Inc

FDA Devices Moderate Mar 15, 2023

Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.

Linet Spol. S.r.o.

FDA Devices Moderate Mar 15, 2023

CardioMEMS HF System PA Sensor and Delivery System, Model Number CM3000, The CardioMEMS HF System provides pulmonary artery (PA) hemodynamic data use…

St. Jude Medical

FDA Devices Moderate Mar 15, 2023

Tri-Staple 2.0 Black Intelligent Reload, Product Number SIG60AXT

Covidien, LP

FDA Devices Moderate Mar 15, 2023

CardioMEMS HF System Hospital Electronics System (HES), Model number CM3000, The CardioMEMS HF System provides pulmonary artery (PA) hemodynamic data…

St. Jude Medical

FDA Devices Moderate Mar 15, 2023

Simplexa COVID-19 Direct, REF: MOL4150; including Reaction Mix, REF: MOL4150; with previous assay definition v2

DiaSorin Molecular LLC

FDA Devices Moderate Mar 15, 2023

BIOPHEN Protein C 5 kit is for in vitro quantitative determination of Protein C activity on human citrated plasma. Protein C is a glycoprotein, vitam…

Aniara Diagnostica LLC

FDA Devices Moderate Mar 15, 2023

LATITUDE NXT Remote Patient Management System, LATITUDE NXT System Server Software Model 6460.

Boston Scientific Corporation

FDA Devices Moderate Mar 15, 2023

CD5 Series of Genesis Reusable Rigid Sterilization Container Systems catalog number and product name: 1. CD5-3B, CONTAINER SHALLOW LG ENDO 3IN PE…

Carefusion 2200 Inc

FDA Devices Moderate Mar 15, 2023

CardioMEMS HF System Patient Electronics System (PES), Model number CM1010, The CardioMEMS HF System provides pulmonary artery (PA) hemodynamic data …

St. Jude Medical

FDA Devices Moderate Mar 15, 2023

epoc Host 2 as follows: Product SMN epoc Host 10736387 epoc Host 2, Canada 10736388 epoc Host 2, China 10736389 epoc Host 2, …

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Mar 15, 2023

Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory to disposable administration set for peritoneal dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Mar 15, 2023

CardioMEMS HF System Patient Electronics System (PES), Model number CM1000, The CardioMEMS HF System provides pulmonary artery (PA) hemodynamic data …

St. Jude Medical

FDA Devices Moderate Mar 15, 2023

Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-34, 0998-00-0800-35…

Datascope Corp.

FDA Devices Moderate Mar 15, 2023

Simplexa Flu A/B & RSV Direct Gen II, REF: MOL2655; including Reaction Mix REF: MOL2656; with previous assay definition v5.

DiaSorin Molecular LLC

FDA Devices Moderate Mar 15, 2023

epoc Host 2 as follows: Product SMN epoc NXS Host, US 11413475 epoc NXS Host, EU 11413497 epoc NXS Host, Japan 11413498 …

Siemens Healthcare Diagnostics Inc

FDA Devices Critical Mar 15, 2023

Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-00-1801, Model Numbers 0998-00-0800-75, 0998-00-0…

Datascope Corp.

FDA Devices Critical Mar 15, 2023

Cardiosave Rescue Model Nos. 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85

Datascope Corp.

FDA Devices Moderate Mar 15, 2023

CardioMEMS HF System Patient Electronics System (PES), Model number CM1100, The CardioMEMS HF System provides pulmonary artery (PA) hemodynamic data …

St. Jude Medical

FDA Devices Critical Mar 15, 2023

Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-00-1801, Model Numbers 0998-00-0800-31, 0998-00-0…

Datascope Corp.

FDA Devices Moderate Mar 15, 2023

Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis

Stryker Leibinger GmbH & Co. KG

NHTSA Critical Mar 10, 2023

FORD 2021-2022: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

FORD

NHTSA Critical Mar 10, 2023

FORD 2022: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:CALIPER

FORD

NHTSA Critical Mar 10, 2023

FORD 2021: VISIBILITY:WINDSHIELD WIPER/WASHER:LINKAGES

FORD

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 August 2026.